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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Synaptic Neurosci.</journal-id>
<journal-title>Frontiers in Synaptic Neuroscience</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Synaptic Neurosci.</abbrev-journal-title>
<issn pub-type="epub">1663-3563</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fnsyn.2020.594484</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Neuroscience</subject>
<subj-group>
<subject>Review</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>The Good, the Bad and the Unknown Aspects of Ghrelin in Stress Coping and Stress-Related Psychiatric Disorders</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name><surname>Fritz</surname> <given-names>Eva Maria</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/405194/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Singewald</surname> <given-names>Nicolas</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/9894/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>De Bundel</surname> <given-names>Dimitri</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x002A;</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/102260/overview"/>
</contrib>
</contrib-group>
<aff id="aff1"><sup>1</sup><institution>Department of Pharmacology and Toxicology, Institute of Pharmacy and CMBI, University of Innsbruck</institution>, <addr-line>Innsbruck</addr-line>, <country>Austria</country></aff>
<aff id="aff2"><sup>2</sup><institution>Department of Pharmaceutical Sciences, Research Group Experimental Pharmacology, Center for Neurosciences (C4N), Vrije Universiteit Brussel</institution>, <addr-line>Brussels</addr-line>, <country>Belgium</country></aff>
<author-notes>
<fn fn-type="edited-by"><p>Edited by: Sigismund Huck, Medical University of Vienna, Austria</p></fn>
<fn fn-type="edited-by"><p>Reviewed by: Wulf Eckhard Haubensak, Research Institute of Molecular Pathology (IMP), Austria; Harriet Schellekens, University College Cork, Ireland</p></fn>
<corresp id="c001">&#x002A;Correspondence: Dimitri De Bundel, <email>dimitri.de.bundel@vub.be</email></corresp>
</author-notes>
<pub-date pub-type="epub">
<day>27</day>
<month>10</month>
<year>2020</year>
</pub-date>
<pub-date pub-type="collection">
<year>2020</year>
</pub-date>
<volume>12</volume>
<elocation-id>594484</elocation-id>
<history>
<date date-type="received">
<day>13</day>
<month>08</month>
<year>2020</year>
</date>
<date date-type="accepted">
<day>14</day>
<month>09</month>
<year>2020</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x00A9; 2020 Fritz, Singewald and De Bundel.</copyright-statement>
<copyright-year>2020</copyright-year>
<copyright-holder>Fritz, Singewald and De Bundel</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/"><p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p></license>
</permissions>
<abstract>
<p>Ghrelin is a peptide hormone released by specialized X/A cells in the stomach and activated by acylation. Following its secretion, it binds to ghrelin receptors in the periphery to regulate energy balance, but it also acts on the central nervous system where it induces a potent orexigenic effect. Several types of stressors have been shown to stimulate ghrelin release in rodents, including nutritional stressors like food deprivation, but also physical and psychological stressors such as foot shocks, social defeat, forced immobilization or chronic unpredictable mild stress. The mechanism through which these stressors drive ghrelin release from the stomach lining remains unknown and, to date, the resulting consequences of ghrelin release for stress coping remain poorly understood. Indeed, ghrelin has been proposed to act as a stress hormone that reduces fear, anxiety- and depression-like behaviors in rodents but some studies suggest that ghrelin may - in contrast - promote such behaviors. In this review, we aim to provide a comprehensive overview of the literature on the role of the ghrelin system in stress coping. We discuss whether ghrelin release is more than a byproduct of disrupted energy homeostasis following stress exposure. Furthermore, we explore the notion that ghrelin receptor signaling in the brain may have effects independent of circulating ghrelin and in what way this might influence stress coping in rodents. Finally, we examine how the ghrelin system could be utilized as a therapeutic avenue in stress-related psychiatric disorders (with a focus on anxiety- and trauma-related disorders), for example to develop novel biomarkers for a better diagnosis or new interventions to tackle relapse or treatment resistance in patients.</p>
</abstract>
<kwd-group>
<kwd>ghrelin</kwd>
<kwd>GHSR</kwd>
<kwd>stress</kwd>
<kwd>anxiety disorders</kwd>
<kwd>PTSD</kwd>
<kwd>central ghrelin resistance</kwd>
<kwd>food intake</kwd>
</kwd-group><counts>
<fig-count count="1"/>
<table-count count="2"/>
<equation-count count="0"/>
<ref-count count="247"/>
<page-count count="23"/>
<word-count count="0"/>
</counts>
</article-meta>
</front>
<body>
<sec id="S1">
<title>The Ghrelin System</title>
<sec id="S1.SS1">
<title>Ghrelin</title>
<p>Ghrelin is a stomach-derived peptide hormone that is tonically released into the blood stream with peak concentrations in response to a negative energy balance (<xref ref-type="bibr" rid="B120">Kojima et al., 1999</xref>; <xref ref-type="bibr" rid="B121">Kojima and Kangawa, 2005</xref>). The 28-amino-acid hormone is primarily produced by X/A-like oxyntic gland cells in the gastric mucosa from its precursor pre-proghrelin (117 amino acids) (<xref ref-type="bibr" rid="B120">Kojima et al., 1999</xref>; <xref ref-type="bibr" rid="B45">Date et al., 2000</xref>). In addition, ghrelin expression has also been described in other organs such as the pancreas, kidneys, lungs, heart and placenta (<xref ref-type="bibr" rid="B159">Mori et al., 2000</xref>; <xref ref-type="bibr" rid="B68">Gualillo et al., 2001</xref>; <xref ref-type="bibr" rid="B64">Gnanapavan et al., 2002</xref>; <xref ref-type="bibr" rid="B93">Iglesias et al., 2004</xref>; <xref ref-type="bibr" rid="B106">Kageyama et al., 2005</xref>).</p>
<p>Ghrelin O-acyltransferase (GOAT) is the enzyme present in the endoplasmatic reticulum of ghrelin-producing cells that ensures the post-translational acylation of desacyl ghrelin (DAG) at the serine-3 residue, resulting in the formation of acyl ghrelin (AG) (<xref ref-type="bibr" rid="B73">Gutierrez et al., 2008</xref>). Both, DAG and AG, are released into the blood stream where AG is rapidly converted to DAG (<xref ref-type="bibr" rid="B48">De Vriese et al., 2004</xref>), resulting in an AG/DAG ratio of 0.1&#x2013;0.4 in plasma compared to 2.5 in stomach tissue (<xref ref-type="bibr" rid="B82">Hassouna et al., 2014</xref>). While DAG has received less attention in literature, an increasing amount of evidence indicates that it is not only a byproduct of AG synthesis but may act as a separate hormone that modulates or even opposes the effects of AG (for review see <xref ref-type="bibr" rid="B49">Delhanty et al., 2014</xref>). For example, DAG was shown to impair the feeding response to peripherally injected AG (<xref ref-type="bibr" rid="B57">Fernandez et al., 2016</xref>) and its actions on anxiety and other stress-related behaviors may also be distinct from those of AG (<xref ref-type="bibr" rid="B218">Stark et al., 2016</xref>; <xref ref-type="bibr" rid="B143">Mahbod et al., 2018</xref>). In this review, we aim to analyze the effects of AG and DAG separately and use the term &#x2018;ghrelin&#x2019; whenever it was not possible to make a clear distinction or acylation status was not specified by the authors.</p>
</sec>
<sec id="S1.SS2">
<title>Ghrelin Receptors (GHSR)</title>
<p>The N-terminus of AG binds with high affinity to the growth hormone secretagogue receptor (GHSR) (<xref ref-type="bibr" rid="B234">Willesen et al., 1999</xref>; <xref ref-type="bibr" rid="B39">Cowley et al., 2003</xref>), of which two different transcripts have been identified: GHSR-1a and GHSR-1b (<xref ref-type="bibr" rid="B150">McKee et al., 1997</xref>). The GHSR-1a, also known as ghrelin receptor (and hereafter simply referred to as &#x2018;GHSR&#x2019;), is a Gq-protein coupled receptor comprising seven transmembrane &#x03B1;-helical domains to which constitutive activity has been ascribed (<xref ref-type="bibr" rid="B87">Holst et al., 2003</xref>). The GHSR-1b form, a truncated splice variant, contains five transmembrane domains and while its physiological role remains poorly understood, it may negatively influence GHSR function by hindering conformational changes (<xref ref-type="bibr" rid="B133">Leung et al., 2007</xref>). AG is the main known high-affinity agonist for the GHSR, while (in physiological concentrations) DAG does not appear to act on the GHSR (<xref ref-type="bibr" rid="B20">Bednarek et al., 2000</xref>). A recent study indicates that the octanoyl chain is essential for the pharmacological action of AG and that DAG, while it might bind to the GHSR with very low affinity, is unlikely to stabilize an active GHSR conformation (<xref ref-type="bibr" rid="B58">Ferre et al., 2019</xref>). Several binding studies propose the existence of a separate receptor specific for DAG in different tissues and also the brain (e.g., <xref ref-type="bibr" rid="B131">Lear et al., 2010</xref>; <xref ref-type="bibr" rid="B225">Togliatto et al., 2010</xref>; <xref ref-type="bibr" rid="B57">Fernandez et al., 2016</xref>). However, such a receptor has not yet been identified (for review see <xref ref-type="bibr" rid="B30">Callaghan and Furness, 2014</xref>).</p>
<p>The GHSR is expressed in several organs such as the brain, the anterior pituitary, adrenal and thyroid glands, pancreas and the heart (<xref ref-type="bibr" rid="B69">Guan et al., 1997</xref>; <xref ref-type="bibr" rid="B64">Gnanapavan et al., 2002</xref>). Within the brain, GHSR expression has been described in several areas including the arcuate nucleus (ARC) and other subregions of the hypothalamus, the ventral tegmental area (VTA), the nucleus tractus solitarius (NTS), the hippocampus and the amygdala (<xref ref-type="bibr" rid="B246">Zigman et al., 2006</xref>; <xref ref-type="bibr" rid="B144">Mani et al., 2014</xref>). The function the GHSR has in those brain areas and whether they are accessible for circulating ghrelin is not yet fully understood (<xref ref-type="bibr" rid="B175">Perello et al., 2018</xref>). Thus, it is essential to note that the GHSR is constitutively active, signaling at 50% of its maximal activity in the absence of its ligand (<xref ref-type="bibr" rid="B87">Holst et al., 2003</xref>; <xref ref-type="bibr" rid="B177">Petersen et al., 2009</xref>). It is very likely that the function of the ghrelin/GHSR system is not solely dependent on the binding of AG to its receptor, but that also changes in GHSR expression levels might have pervasive biological effects. Furthermore, there is evidence that the GHSR can form heterodimers with various other receptors like for example those for dopamine, serotonin or oxytocin (<xref ref-type="bibr" rid="B201">Schellekens et al., 2013b</xref>; <xref ref-type="bibr" rid="B113">Kern et al., 2015</xref>; <xref ref-type="bibr" rid="B230">Wallace Fitzsimons et al., 2019</xref>), which affects downstream signaling and receptor trafficking (for review see <xref ref-type="bibr" rid="B199">Schellekens et al., 2013a</xref>; <xref ref-type="bibr" rid="B2">Abizaid and Hougland, 2020</xref>). Recent findings also suggest that the liver-expressed antimicrobial peptide 2 (LEAP2) acts as an endogenous antagonist/inverse agonist of the GHSR that modulates ghrelin function in response to the feeding status (<xref ref-type="bibr" rid="B61">Ge et al., 2018</xref>).</p>
</sec>
<sec id="S1.SS3">
<title>The Ghrelin System and Energy Homeostasis</title>
<p>Ghrelin is most widely known for its orexigenic effects. Following its release into the bloodstream, AG can diffuse passively through fenestrated capillaries of the median eminence into the ARC (<xref ref-type="bibr" rid="B195">Schaeffer et al., 2013</xref>) where it binds to GHSR that are expressed abundantly on neuropeptide Y/agouti-related peptide (NPY/AGRP) neurons (<xref ref-type="fig" rid="F1">Figure 1</xref>) (<xref ref-type="bibr" rid="B234">Willesen et al., 1999</xref>; <xref ref-type="bibr" rid="B39">Cowley et al., 2003</xref>). Activation of these hypothalamic neurons by AG potently increases food intake and regulates homeostatic feeding behavior in order to maintain energy balance (<xref ref-type="bibr" rid="B108">Kamegai et al., 2000</xref>; <xref ref-type="bibr" rid="B163">Nakazato et al., 2001</xref>). Indeed, re-expression of GHSR in AGRP neurons of GHSR KO mice restores, albeit incompletely, the effect of systemic administration of AG on food intake (<xref ref-type="bibr" rid="B231">Wang et al., 2014</xref>). In addition, ghrelin also plays an important role in reward-based, hedonic eating behaviors (as reviewed in <xref ref-type="bibr" rid="B176">Perello and Zigman, 2012</xref>; <xref ref-type="bibr" rid="B6">Al Massadi et al., 2019</xref>), which are very likely mediated by GHSR on dopaminergic neurons of the VTA (<xref ref-type="bibr" rid="B37">Cornejo et al., 2020</xref>).</p>
<fig id="F1" position="float">
<label>FIGURE 1</label>
<caption><p>The ghrelin system in stress coping. In periods of hunger and stress, AG is produced by acylation of DAG by GOAT in gastric X/A cells and released into the blood stream. Before it is degraded to DAG, it acts on GHSR in the arcuate nucleus of the hypothalamus (ARC) to regulate homeostatic feeding. Increased AG levels during stress also seem to amplify HPA axis activation and induce corticosterone (CORT) release. The exact mechanism is not clear and could involve indirect activation of CRF-producing neurons in the PVN by inhibition of the local GABAergic tone, modulation of ACTH production in the pituitary (PIT) or direct effects on the adrenal cortex (ADR). AG may also indirectly influence the HPA axis via GHSR in the nodose ganglion (NG) of the vagal nerve or in the nucleus tractus solitarius (NTS). Conversely, whether HPA axis activity during stress has an impact on ghrelin release remains a subject of debate. Elevated AG levels following stress may also be secondary to activation of the sympathetic nervous system and beta receptors on ghrelin-producing X/A cells. Whether AG can pass the blood-brain barrier to act on stress-relevant brain areas where GHSR are expressed is not clear. However, constitutive activity of central GHSR may be regulated via changes in GHSR expression levels or formation of heterodimers with other receptors (e.g., dopamine, serotonin) as co-regulators. Such mechanisms might play a role in stress-related changes in feeding and fear, anxiety- and depression like behaviors, possibly via GHSR in the ventral tegmental area (VTA), hippocampus (HPC) and amygdala (AMY). Also mesocorticolimbic dopaminergic projections (DA) of the VTA to nucleus accumbens (NAc), medial prefrontal cortex (mPFC), HPC and AMY may play a role here. <italic>Abbreviations:</italic> AG, acyl ghrelin; DAG, desacyl ghrelin; GOAT, ghrelin O-acyltransferase; BChE, butyryl cholinesterase; ARC, arcuate nucleus of the hypothalamus; PVN, paraventricular nucleus of the hypothalamus; CRF, corticotropin releasing factor; PIT, pituitary gland; ACTH, adrenocorticotropic hormone; CORT, corticosterone/cortisol; ADR, adrenal cortex; NTS, nucleus tractus solitarius; NG, nodose ganglion; VTA, ventral tegmental area; PBN, parabrachial nucleus; DA, dopamine; NAc, nucleus accumbens; mPFC, medial prefrontal cortex; HPC, hippocampus; AMY, amygdala.</p></caption>
<graphic xlink:href="fnsyn-12-594484-g001.tif"/>
</fig>
<p>In humans, plasma ghrelin levels are typically increased under low-calorie conditions before meals and fall back to baseline levels after food consumption (<xref ref-type="bibr" rid="B42">Cummings, 2006</xref>). Also in rodents, ghrelin plasma levels rise during fasting periods and follow a diurnal rhythm peaking shortly after onset of the dark period, which is the major feeding time for rodents (<xref ref-type="bibr" rid="B160">Murakami et al., 2002</xref>; <xref ref-type="bibr" rid="B22">Bodosi et al., 2004</xref>). Peripherally circulating ghrelin has various effects on the gastrointestinal tract: it modulates intestinal motility, gastric emptying and gastric acid secretion as well as insulin release from the pancreas (for review see <xref ref-type="bibr" rid="B121">Kojima and Kangawa, 2005</xref>).</p>
<p>Overall, the role of ghrelin in driving food intake and energy homeostasis seems well established: it communicates with the brain and the gastrointestinal tract to promote feeding and ensure efficient energy storage and metabolism, lowering the risk of hypoglycemia (reviewed comprehensively by <xref ref-type="bibr" rid="B240">Yanagi et al., 2018</xref>). Importantly, while ghrelin signaling stimulates food intake, the effects of a loss of ghrelin signaling on feeding behavior are more subtle if detectable at all (as reviewed in <xref ref-type="bibr" rid="B227">Uchida et al., 2013</xref>). Nevertheless, ghrelin appears critical in the regulation of systemic glucose homeostasis and ensures survival after prolonged starvation (<xref ref-type="bibr" rid="B65">Goldstein et al., 2011</xref>; <xref ref-type="bibr" rid="B148">McFarlane et al., 2014</xref>), potentially through GHSR signaling in the nodose ganglion (NG) of the vagal nerve and the NTS (<xref ref-type="bibr" rid="B204">Scott et al., 2012</xref>; <xref ref-type="bibr" rid="B167">Okada et al., 2018</xref>) (<xref ref-type="fig" rid="F1">Figure 1</xref>). Projections of the NTS to the parabrachial nucleus (<xref ref-type="bibr" rid="B188">Roman et al., 2016</xref>) and to the ARC (<xref ref-type="bibr" rid="B5">Aklan et al., 2020</xref>) were shown to regulate food intake in anorectic or hypoglycemic conditions, but it remains poorly understood how the ghrelin system modulates activity in these neurochemically distinct pathways. The effect of ghrelin on glucose homeostasis also involves the release of growth hormone in response to low blood glucose if body fat stores are depleted, which in turn increases glucose release from the liver and contributes to stabilization of blood glucose levels (<xref ref-type="bibr" rid="B65">Goldstein et al., 2011</xref>). Moreover, ghrelin modulates pancreatic insulin secretion and regulates its peripheral actions, although the exact mechanisms involved are still a matter of debate (as reviewed by <xref ref-type="bibr" rid="B67">Gray et al., 2019</xref>). Interestingly, it has been proposed that a decline in ghrelin system activity may play a role in age-dependent impairment of energy homeostasis and associated disease patterns like reduced appetite, obesity, diabetes or hepatic steatosis, but also cardiovascular dysfunction and neurodegenerative diseases (for review see <xref ref-type="bibr" rid="B222">Stoyanova, 2014</xref>; <xref ref-type="bibr" rid="B242">Yin and Zhang, 2016</xref>; <xref ref-type="bibr" rid="B10">Amitani et al., 2017</xref>).</p>
</sec>
<sec id="S1.SS4">
<title>Ghrelin/GHSR Interactions With the HPA Axis</title>
<p>Beyond its well-established role as a mediator of feeding behavior, the ghrelin system has also been implicated in many other functions. Notably, it has been proposed as a regulator of stress responses, as its function seems to be closely entwined with that of the hypothalamic-pituitary-adrenal (HPA) axis (for review see <xref ref-type="bibr" rid="B216">Spencer et al., 2015</xref>), as illustrated in <xref ref-type="fig" rid="F1">Figure 1</xref>.</p>
<p>Several studies have demonstrated that systemic or central administration of ghrelin increases the plasma concentration of corticosterone in rodents or cortisol in humans (<xref ref-type="bibr" rid="B12">Asakawa et al., 2001a</xref>; <xref ref-type="bibr" rid="B220">Stevanovic et al., 2007</xref>; <xref ref-type="bibr" rid="B128">Lambert et al., 2011</xref>; <xref ref-type="bibr" rid="B28">Cabral et al., 2012</xref>, <xref ref-type="bibr" rid="B27">2016</xref>; <xref ref-type="bibr" rid="B97">Jensen et al., 2016</xref>). The effects of ghrelin on plasma adrenocorticotropic hormone (ACTH), however, appear inconsistent. One study reported elevated ACTH and an increased volume of ACTH-producing cells in the pituitary following central ghrelin administration (<xref ref-type="bibr" rid="B220">Stevanovic et al., 2007</xref>), but another study found no influence of ghrelin on plasma ACTH levels (<xref ref-type="bibr" rid="B97">Jensen et al., 2016</xref>). In line with the notion that the ghrelin system may increase activity of the HPA axis, a blunted release of ACTH and corticosterone after exposure to a brief period of immobilization stress was previously observed in ghrelin KO mice (<xref ref-type="bibr" rid="B217">Spencer et al., 2012</xref>). Similarly, one study showed lower corticosterone levels in GHSR KO compared to wild type mice in a chronic social defeat stress (CSDS) paradigm (<xref ref-type="bibr" rid="B35">Chuang et al., 2011</xref>). In contrast to the aforementioned studies, a more recent publication reported higher corticosterone release after acute restraint stress in non-handled ghrelin KO mice versus wild type controls (<xref ref-type="bibr" rid="B143">Mahbod et al., 2018</xref>). Moreover, more elevated plasma corticosterone levels have also been observed in GHSR KO mice following acute and chronic stress paradigms (<xref ref-type="bibr" rid="B173">Patterson et al., 2013a</xref>; <xref ref-type="bibr" rid="B143">Mahbod et al., 2018</xref>). Interestingly, administration of DAG increased plasma corticosterone levels in non-stressful conditions in ghrelin KO mice, but attenuated corticosterone release during acute stress exposure (<xref ref-type="bibr" rid="B218">Stark et al., 2016</xref>), suggesting that the effects of DAG on HPA axis activity may depend on prior stress exposure.</p>
<p>Taken together, the influence of the ghrelin system on HPA axis activity is not fully resolved yet and the underlying mechanisms remain poorly understood. Cabral and colleagues demonstrated that peripheral AG administration induces c-Fos expression not only in the ARC but also in corticotropin releasing factor (CRF)-producing cells in the paraventricular nucleus (PVN) of the hypothalamus (<xref ref-type="bibr" rid="B28">Cabral et al., 2012</xref>). These cells, however, do not express GHSR, so in a further study the authors suggested that AG may indirectly activate CRF neurons in the PVN via inhibition of the local GABAergic tone (<xref ref-type="bibr" rid="B28">Cabral et al., 2012</xref>, <xref ref-type="bibr" rid="B27">2016</xref>), which was confirmed by a more recent electrophysiological study (<xref ref-type="bibr" rid="B50">Dos-Santos et al., 2018</xref>). Ghrelin may also influence the HPA axis through other mechanisms (<xref ref-type="fig" rid="F1">Figure 1</xref>). Intravenous administration of ghrelin appears to inhibit vagal afferents (<xref ref-type="bibr" rid="B13">Asakawa et al., 2001b</xref>; <xref ref-type="bibr" rid="B46">Date et al., 2006</xref>) and stimulate vagal efferents (<xref ref-type="bibr" rid="B60">Fujitsuka et al., 2011</xref>). The influence of the ghrelin system on activity of the vagal nerve remains controversial (<xref ref-type="bibr" rid="B11">Arnold et al., 2006</xref>) and may involve activation of GHSR in the NG of the vagal nerve or central mechanisms with activation of GHSR in the NTS (<xref ref-type="bibr" rid="B17">Bansal et al., 2012</xref>; <xref ref-type="bibr" rid="B224">Swartz et al., 2014</xref>; <xref ref-type="bibr" rid="B223">Su et al., 2019</xref>). Further elucidation of the interaction of the ghrelin system with the vagus nerve may be relevant in this context, given that vagal nerve stimulation influences HPA axis activity in rodents (<xref ref-type="bibr" rid="B47">De Herdt et al., 2009</xref>) and humans (<xref ref-type="bibr" rid="B232">Warren et al., 2019</xref>). Moreover, ghrelin may also have an impact on glucocorticoid production through direct effects on the adrenal gland (<xref ref-type="bibr" rid="B191">Rucinski et al., 2009</xref>).</p>
<p>Conversely, how activity in the HPA axis may influence the ghrelin system also remains subject of debate (<xref ref-type="fig" rid="F1">Figure 1</xref>). Administration of an ACTH analog was shown to increase plasma ghrelin levels in humans by increasing cortisol levels (<xref ref-type="bibr" rid="B14">Azzam et al., 2017</xref>). On the other hand, chronic immobilization stress increased plasma AG levels in adrenalectomized rats (<xref ref-type="bibr" rid="B153">Meyer et al., 2014</xref>), indicating that stress can drive AG release independently of glucocorticoid production. Interestingly, a recent study demonstrated that elevated AG levels following chronic stress exposure could be reversed by the beta receptor antagonist atenolol (<xref ref-type="bibr" rid="B72">Gupta et al., 2019</xref>). This hydrophilic beta receptor antagonist does not readily cross the blood-brain barrier, suggesting that stress-induced elevations in plasma AG may be secondary to activation of the sympathetic nervous system.</p>
<p>The notion that ghrelin is released upon stress exposure and mediates at least some behavioral adaptations to stress, which we review and discuss in the following two sections, supports the idea of ghrelin as a novel stress hormone, acting in concert with but also partially independent of the central HPA axis.</p>
</sec>
</sec>
<sec id="S2">
<title>The Role of the Ghrelin System in Stress-Related Behaviors in Rodents</title>
<sec id="S2.SS1">
<title>Effects of Stress on Plasma Ghrelin Levels in Rodents</title>
<p>There is ample evidence showing that plasma ghrelin levels are affected by various acute and chronic stressors, as summarized in <xref ref-type="table" rid="T1">Table 1</xref>. Increased total ghrelin levels were reported following acute water avoidance stress in rats (<xref ref-type="bibr" rid="B124">Kristenssson et al., 2006</xref>, <xref ref-type="bibr" rid="B123">Kristenssson et al., 2007</xref>) or maternal separation in mice (<xref ref-type="bibr" rid="B202">Schmidt et al., 2006</xref>), while elevated DAG but not AG was observed in plasma of rats following a short immobilization stress episode (<xref ref-type="bibr" rid="B161">Nahata et al., 2014</xref>). A number of publications also showed no changes in AG or total ghrelin levels after a single exposure to foot shocks (<xref ref-type="bibr" rid="B80">Harmatz et al., 2016</xref>; <xref ref-type="bibr" rid="B189">Rostamkhani et al., 2016</xref>) or immobilization stress in rats (<xref ref-type="bibr" rid="B70">Gul et al., 2017</xref>). Importantly, nutritional status may also play a role, given that acute stressors such as novelty stress (<xref ref-type="bibr" rid="B192">Saegusa et al., 2011</xref>) or a single injection of lipopolysaccharide (LPS) (<xref ref-type="bibr" rid="B219">Stengel et al., 2010</xref>) led to a decrease in plasma AG alone or both, DAG and AG, when blood samples were collected in food-deprived conditions.</p>
<table-wrap position="float" id="T1">
<label>TABLE 1</label>
<caption><p>Effect of stressors on ghrelin levels in rodents.</p></caption>
<table cellspacing="5" cellpadding="5" frame="hsides" rules="groups">
<thead>
<tr>
<td valign="top" align="left">References</td>
<td valign="top" align="center">Animals</td>
<td valign="top" align="center">Feeding status</td>
<td valign="top" align="center">Duration</td>
<td valign="top" align="center">Stress paradigm</td>
<td valign="top" align="center">Ghrelin levels</td>
<td valign="top" align="center">Time point</td>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B124">Kristenssson et al., 2006</xref>) (<xref ref-type="bibr" rid="B123">Kristenssson et al., 2007</xref>)</td>
<td valign="top" align="center"><bold>rats (WKY, SPD)</bold> f</td>
<td valign="top" align="center"><italic>ad libitum</italic> fed</td>
<td valign="top" align="center"><bold>acute</bold></td>
<td valign="top" align="center"><bold>water avoidance</bold> 1 h</td>
<td valign="top" align="center">TG &#x2191; <bold>(WKY</bold> &#x003E; <bold>SPD)</bold></td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B202">Schmidt et al., 2006</xref>)</td>
<td valign="top" align="center"><bold>mice (CD1)</bold> m/f, pups (p8)</td>
<td valign="top" align="center">not specified</td>
<td valign="top" align="center"><bold>acute</bold></td>
<td valign="top" align="center"><bold>maternal separation</bold> 4 h, 8 h, 12 h</td>
<td valign="top" align="center">?G &#x2191;</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B161">Nahata et al., 2014</xref>)</td>
<td valign="top" align="center"><bold>mice (ICR)</bold> m</td>
<td valign="top" align="center">fasted + fed (16 h + 20 min)</td>
<td valign="top" align="center"><bold>acute</bold></td>
<td valign="top" align="center"><bold>immobilization stress</bold> 1 h</td>
<td valign="top" align="center">AG &#x2194; DAG &#x2191;</td>
<td valign="top" align="center">@ during immobilization</td>
</tr>
<tr>
<td/>
<td/>
<td valign="top" align="left" colspan="5"><hr/></td>
</tr>
<tr>
<td valign="top" align="justify"/>
<td valign="top" align="justify"/>
<td valign="top" align="center">fasted (16 h)</td>
<td valign="top" align="center"><bold>acute</bold></td>
<td valign="top" align="center"><bold>immobilization stress</bold> 1 h</td>
<td valign="top" align="center">AG &#x2194; DAG &#x2191;</td>
<td valign="top" align="center">@ during immobilization</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B80">Harmatz et al., 2016</xref>)</td>
<td valign="top" align="center"><bold>rats (LE)</bold> m</td>
<td valign="top" align="center"><italic>ad libitum</italic> fed</td>
<td valign="top" align="center"><bold>acute</bold></td>
<td valign="top" align="center"><bold>foot shock</bold> 3 &#x00D7; 2s</td>
<td valign="top" align="center">AG &#x2194;</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B189">Rostamkhani et al., 2016</xref>)</td>
<td valign="top" align="center"><bold>rats (WST)</bold> m</td>
<td valign="top" align="center"><italic>ad libitum</italic> fed</td>
<td valign="top" align="center"><bold>acute</bold></td>
<td valign="top" align="center"><bold>foot shock</bold> 60 &#x00D7; 10s</td>
<td valign="top" align="center">TG &#x2194;</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B70">Gul et al., 2017</xref>)</td>
<td valign="top" align="center"><bold>rats (WST)</bold> m</td>
<td valign="top" align="center"><italic>ad libitum</italic> fed</td>
<td valign="top" align="center"><bold>acute</bold></td>
<td valign="top" align="center"><bold>immobilization stress</bold> 2 h</td>
<td valign="top" align="center">?G &#x2194;</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B192">Saegusa et al., 2011</xref>)</td>
<td valign="top" align="center"><bold>mice (C57BL/6J)</bold> m</td>
<td valign="top" align="center">fasted (24 h)</td>
<td valign="top" align="center"><bold>acute</bold></td>
<td valign="top" align="center"><bold>novelty (single housing)</bold> 3 h</td>
<td valign="top" align="center">AG &#x2193;</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B219">Stengel et al., 2010</xref>)</td>
<td valign="top" align="center"><bold>rats (SPD)</bold> m</td>
<td valign="top" align="center">fasted (17 h)</td>
<td valign="top" align="center"><bold>acute</bold></td>
<td valign="top" align="center"><bold>LPS injection</bold> 100 &#x03BC;g/kg</td>
<td valign="top" align="center">AG &#x2193; \ &#x2194; DAG &#x2193;\&#x2194;</td>
<td valign="top" align="center">@ 2 h, 5 h, 7 h \ 24 h</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B165">Ochi et al., 2008</xref>)</td>
<td valign="top" align="center"><bold>rats (WST)</bold> m</td>
<td valign="top" align="center"><italic>ad libitum</italic> fed</td>
<td valign="top" align="center"><bold>subchronic</bold></td>
<td valign="top" align="center"><bold>water cage</bold> 5 d</td>
<td valign="top" align="center">TG &#x2194; \ &#x2194; AG &#x2194; \ &#x2191; DAG &#x2194; \ &#x2194;</td>
<td valign="top" align="center">@ 4 h, 8h, 24 h \ 3 d, 5 d</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B238">Yamada et al., 2015</xref>)</td>
<td valign="top" align="center"><bold>mice (C57BL/6)</bold> m/f</td>
<td valign="top" align="center">fasted (18 h)</td>
<td valign="top" align="center"><bold>subchronic</bold></td>
<td valign="top" align="center"><bold>social isolation</bold> 7 d</td>
<td valign="top" align="center">AG &#x2191; <bold>m</bold> vs. &#x2194; <bold>f</bold></td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B95">Izadi et al., 2018</xref>)</td>
<td valign="top" align="center"><bold>rats (WST)</bold> m</td>
<td valign="top" align="center">fasted (16&#x2013;18 h)</td>
<td valign="top" align="center"><bold>subchronic</bold></td>
<td valign="top" align="center"><bold>social stress</bold> 7 d</td>
<td valign="top" align="center">?G &#x2194;</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td/>
<td/>
<td/>
<td valign="top" align="left" colspan="4"><hr/></td>
</tr>
<tr>
<td valign="top" align="justify"/>
<td valign="top" align="justify"/>
<td valign="top" align="justify"/>
<td valign="top" align="center"><bold>subchronic</bold></td>
<td valign="top" align="center"><bold>social isolation</bold> 7 d</td>
<td valign="top" align="center">?G &#x2193;</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B237">Yam et al., 2017</xref>)</td>
<td valign="top" align="center"><bold>mice (C57BL/6J)</bold> m/f, pups (p2-p14)</td>
<td valign="top" align="center">not specified</td>
<td valign="top" align="center"><bold>subchronic</bold></td>
<td valign="top" align="center"><bold>early chronic stress</bold> 7 d (p2-p9)</td>
<td valign="top" align="center">TG &#x2194; \ &#x2194; <bold>m</bold> vs. &#x2191; \ &#x2193; <bold>f</bold> AG &#x2194; \ &#x2194; <bold>m</bold> vs. &#x2194; \ &#x2194; <bold>f</bold> DAG &#x2194; \ &#x2194; <bold>m</bold> vs. &#x2191; \ &#x2193; <bold>f</bold></td>
<td valign="top" align="center">@ p9 \ p14</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B142">Lutter et al., 2008</xref>)</td>
<td valign="top" align="center"><bold>mice (C57BL/6J)</bold> m</td>
<td valign="top" align="center"><italic>ad libitum</italic> fed</td>
<td valign="top" align="center"><bold>chronic</bold></td>
<td valign="top" align="center"><bold>CSDS</bold> 10 d</td>
<td valign="top" align="center">AG &#x2191; \ &#x2191;</td>
<td valign="top" align="center">@ 11d \ 39d</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B35">Chuang et al., 2011</xref>)</td>
<td valign="top" align="center"><bold>mice (GHSR WT/KO)</bold> m, C57BL/6J bckg</td>
<td valign="top" align="center"><italic>ad libitum</italic> fed</td>
<td valign="top" align="center"><bold>chronic</bold></td>
<td valign="top" align="center"><bold>CSDS</bold> 10 d</td>
<td valign="top" align="center">AG &#x2191; (<bold>GHSR KO</bold> and <bold>WT</bold>) DAG &#x2194; (<bold>GHSR KO</bold> and <bold>WT</bold>)</td>
<td valign="top" align="center"></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B173">Patterson et al., 2013a</xref>)</td>
<td valign="top" align="center"><bold>mice (C57BL/6J)</bold> m</td>
<td valign="top" align="center"><italic>ad libitum</italic> fed (STD + HFD)</td>
<td valign="top" align="center"><bold>chronic</bold></td>
<td valign="top" align="center"><bold>CSDS</bold> 21 d</td>
<td valign="top" align="center">AG &#x2191; \ &#x2194;</td>
<td valign="top" align="center">@ 22d \ 62d</td>
</tr>
<tr>
<td valign="top" align="justify"/>
<td valign="top" align="center"><bold>mice (GHSR WT/KO)</bold> m, C57BL/6J bckg</td>
<td valign="top" align="center"><italic>ad libitum</italic> fed (STD + HFD)</td>
<td valign="top" align="center"><bold>chronic</bold></td>
<td valign="top" align="center"><bold>CSDS</bold> 21 d</td>
<td valign="top" align="center">AG &#x2191; (<bold>GHSR WT</bold> only)</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B71">Guo et al., 2019</xref>)</td>
<td valign="top" align="center"><bold>mice (GHSR KO/WT)</bold> m</td>
<td valign="top" align="center"><italic>ad libitum</italic> fed</td>
<td valign="top" align="center"><bold>chronic</bold></td>
<td valign="top" align="center"><bold>CSDS</bold> 10 d</td>
<td valign="top" align="center">TG &#x2191; (<bold>GHSR KO</bold> and <bold>WT</bold>)</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B75">Han et al., 2019</xref>)</td>
<td valign="top" align="center"><bold>C57BL/6J mice</bold> m</td>
<td valign="top" align="center"><italic>ad libitum</italic> fed</td>
<td valign="top" align="center"><bold>chronic</bold></td>
<td valign="top" align="center"><bold>CSDS</bold> 10 d</td>
<td valign="top" align="center">AG &#x2191;</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B185">Razzoli et al., 2015</xref>)</td>
<td valign="top" align="center"><bold>mice (CD1)</bold> m</td>
<td valign="top" align="center"><italic>ad libitum</italic> fed</td>
<td valign="top" align="center"><bold>chronic</bold></td>
<td valign="top" align="center"><bold>CSDS</bold> 28 d</td>
<td valign="top" align="center">TG &#x2193;</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B138">Lopez Lopez et al., 2018</xref>)</td>
<td valign="top" align="center"><bold>rats (WST)</bold> m</td>
<td valign="top" align="center"><italic>ad libitum</italic> fed</td>
<td valign="top" align="center"><bold>chronic</bold></td>
<td valign="top" align="center"><bold>CUMS</bold> 20 d, 40 d, 60 d</td>
<td valign="top" align="center">TG &#x2194; \ &#x2191; \ &#x2194;</td>
<td valign="top" align="center">@ 20 d \ 40 d \ 60 d</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B172">Patterson et al., 2010</xref>)</td>
<td valign="top" align="center"><bold>mice (GHSR WT/KO)</bold> m, C57BL/6J-DBA bckg</td>
<td valign="top" align="center"><italic>ad libitum</italic> fed (STD + HFD)</td>
<td valign="top" align="center"><bold>chronic</bold></td>
<td valign="top" align="center"><bold>CUMS</bold> 14 d</td>
<td valign="top" align="center">AG &#x2191; (<bold>GHSR KO</bold> and <bold>WT</bold>)</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B92">Huang et al., 2017</xref>)</td>
<td valign="top" align="center"><bold>mice (C57BL/6J)</bold> m</td>
<td valign="top" align="center"><italic>ad libitum</italic> fed</td>
<td valign="top" align="center"><bold>chronic</bold></td>
<td valign="top" align="center"><bold>CUMS</bold> 8 w</td>
<td valign="top" align="center">AG &#x2191;</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B54">Elbassuoni, 2014</xref>)</td>
<td valign="top" align="center"><bold>rats (SPD)</bold> m/f</td>
<td valign="top" align="center">fasted (10h)</td>
<td valign="top" align="center"><bold>chronic</bold></td>
<td valign="top" align="center"><bold>immobilization stress</bold> 20 min/d, 21 d</td>
<td valign="top" align="center">?G &#x2191; (<bold>f</bold> &#x003E; <bold>m</bold>)</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B153">Meyer et al., 2014</xref>)</td>
<td valign="top" align="center"><bold>rats (LE)</bold> m</td>
<td valign="top" align="center"><italic>ad libitum</italic> fed</td>
<td valign="top" align="center"><bold>chronic</bold></td>
<td valign="top" align="center"><bold>immobilization stress</bold> 4 h/d, 14 d</td>
<td valign="top" align="center">AG &#x2191;</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B189">Rostamkhani et al., 2016</xref>)</td>
<td valign="top" align="center"><bold>rats (WST)</bold> m</td>
<td valign="top" align="center"><italic>ad libitum</italic> fed</td>
<td valign="top" align="center"><bold>chronic</bold></td>
<td valign="top" align="center"><bold>foot shock</bold> 60 &#x00D7; 10s, 15 d</td>
<td valign="top" align="center">TG &#x2193;</td>
<td valign="top" align="center">&#x2013;</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B243">Yousufzai et al., 2018</xref>)</td>
<td valign="top" align="center"><bold>rats (LE)</bold> m</td>
<td valign="top" align="center"><italic>ad libitum</italic> fed</td>
<td valign="top" align="center"><bold>chronic</bold></td>
<td valign="top" align="center"><bold>immobilization stress</bold> 4 h/d, 14 d</td>
<td valign="top" align="center">AG &#x2191;</td>
<td valign="top" align="center">@ 130 d</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<attrib><italic>Measurements after stressor cessation unless stated otherwise (@ x h/d; 1 = start of stressor). Abbreviations: WKY, Wistar-Kyoto; SPD, Sprague-Dawley; LE, Long-Evans; WST, Wistar; p, postnatal day; bckg, background; STD, standard diet; HFD, high-fat diet; LPS, lipopolysaccharide; CSDS, chronic social defeat stress; CUMS, chronic mild unpredictable stress; TG, total ghrelin; AG, acyl ghrelin; DAG, desacyl ghrelin; ?G, ghrelin (not specified).</italic></attrib>
</table-wrap-foot>
</table-wrap>
<p>In subchronic stress paradigms like exposure of rats to a flooded cage, elevated AG levels were found (<xref ref-type="bibr" rid="B165">Ochi et al., 2008</xref>). Also socially isolated male but not female mice showed increased plasma AG in fasted conditions (<xref ref-type="bibr" rid="B238">Yamada et al., 2015</xref>). However, no changes or even decreases in serum ghrelin levels were reported following subchronic social stress or social isolation in rats in a fasted state (<xref ref-type="bibr" rid="B95">Izadi et al., 2018</xref>). The effects of stress exposure on plasma ghrelin levels may be dependent on developmental stage and sex, given that subchronic stress induced by limited nesting material seemed to affect plasma ghrelin levels differently in male and female mice, with minor alterations in male pups versus pronounced changes in serum DAG in female pups (<xref ref-type="bibr" rid="B237">Yam et al., 2017</xref>).</p>
<p>Regarding chronic stressors, a number of studies reported increased plasma AG levels following CSDS in mice (<xref ref-type="bibr" rid="B142">Lutter et al., 2008</xref>; <xref ref-type="bibr" rid="B35">Chuang et al., 2011</xref>; <xref ref-type="bibr" rid="B173">Patterson et al., 2013a</xref>; <xref ref-type="bibr" rid="B71">Guo et al., 2019</xref>; <xref ref-type="bibr" rid="B75">Han et al., 2019</xref>). Only one study in mice found decreased total ghrelin levels following CSDS (<xref ref-type="bibr" rid="B185">Razzoli et al., 2015</xref>), however, the decrease in total plasma ghrelin was not observed when the food intake was restricted throughout the CSDS paradigm. Similarly, chronic mild unpredictable stress (CUMS) protocols were shown to induce elevated total serum ghrelin levels in rats (<xref ref-type="bibr" rid="B138">Lopez Lopez et al., 2018</xref>) and plasma AG levels in mice (<xref ref-type="bibr" rid="B172">Patterson et al., 2010</xref>; <xref ref-type="bibr" rid="B92">Huang et al., 2017</xref>). Also chronic immobilization stress increased ghrelin or AG levels in rats (<xref ref-type="bibr" rid="B54">Elbassuoni, 2014</xref>; <xref ref-type="bibr" rid="B153">Meyer et al., 2014</xref>). A recent study showed that elevated plasma AG levels following chronic immobilization stress in adolescent rats persisted up to four months after stress exposure (<xref ref-type="bibr" rid="B243">Yousufzai et al., 2018</xref>). Only one study reported decreased total ghrelin levels following repeated exposure to foot shocks (<xref ref-type="bibr" rid="B189">Rostamkhani et al., 2016</xref>). In summary, while literature on the effects of acute or subchronic stress exposure on plasma ghrelin levels is conflicting, chronic exposure to stress relatively consistently increases plasma AG levels.</p>
</sec>
<sec id="S2.SS2">
<title>Effects of Stress on Food Intake and Body Weight in Rodents and the Possible Role of Ghrelin and GHSR Signaling</title>
<p>Exposure to acute and chronic stressors impacts on food intake and body weight in rodents and the ghrelin system has been proposed a role in stress-related feeding behaviors, which, however, is not fully established yet. In <xref ref-type="table" rid="T2">Table 2</xref> we give an extensive, although certainly not exhaustive, overview of the effects of different acute and chronic stress paradigms on food intake and body weight.</p>
<table-wrap position="float" id="T2">
<label>TABLE 2</label>
<caption><p>Effect of stressors on food intake in rodents.</p></caption>
<table cellspacing="5" cellpadding="5" frame="hsides" rules="groups">
<thead>
<tr>
<td valign="top" align="left">References</td>
<td valign="top" align="center">Animals</td>
<td valign="top" align="center">Paradigm <italic>(Feeding status)</italic></td>
<td valign="top" align="center">Food intake (FI)</td>
<td valign="top" align="center">Time point <italic>Measurement</italic></td>
<td valign="top" align="center">Body weight (BW)</td>
<td valign="top" align="center">Time point <italic>Measurement</italic></td>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="center" colspan="7"><bold>Acute stress paradigms</bold></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B151">Meerlo et al., 1996</xref>)</td>
<td valign="top" align="center"><bold>rats (TMDS3)</bold> m</td>
<td valign="top" align="center"><bold>social defeat</bold> 1x or 2x</td>
<td valign="top" align="center">&#x2193; (<bold>2x</bold> only)</td>
<td valign="top" align="center">@ 1 d-3 d <italic>FI daily</italic></td>
<td valign="top" align="center">&#x2194; \ &#x2193; (<bold>2x</bold> &#x003E; <bold>1x</bold>)</td>
<td valign="top" align="center">@ 1 d \ 2 d-3 d <italic>BW g</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B70">Gul et al., 2017</xref>)</td>
<td valign="top" align="center"><bold>rats (WST)</bold> m</td>
<td valign="top" align="center"><bold>immobilization stress</bold> 2 h <italic>(fed)</italic></td>
<td valign="top" align="center">&#x2193;</td>
<td valign="top" align="center">@ 24 h <italic>FI cumul</italic></td>
<td valign="top" align="center">&#x2193;</td>
<td valign="top" align="center">@ 24h <italic>BW change %</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B192">Saegusa et al., 2011</xref>)</td>
<td valign="top" align="center"><bold>mice (C57BL/6J)</bold> m</td>
<td valign="top" align="center"><bold>novelty</bold> 3 h (<italic>fasted, 24h)</italic></td>
<td valign="top" align="center">&#x2193; \ &#x2194;</td>
<td valign="top" align="center">@ 1 h, 3 h \ 6 h <italic>FI cumul</italic></td>
<td valign="top" align="center">-</td>
<td valign="top" align="center">-</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">4&#x002A;(<xref ref-type="bibr" rid="B146">Matsumoto et al., 2017</xref>)</td>
<td valign="top" align="center"><bold>mice (C57BL/6)</bold> f, aged</td>
<td valign="top" align="center"><bold>novelty</bold> 3 h <italic>(fasted, 18 h)</italic></td>
<td valign="top" align="center">&#x2193;</td>
<td valign="top" align="center">@ 1 h, 3 h <italic>FI cumul</italic></td>
<td valign="top" align="center">-</td>
<td valign="top" align="center">-</td>
</tr>
<tr>
<td/>
<td valign="top" align="left" colspan="6"><hr/></td>
</tr>
<tr>
<td/>
<td valign="top" align="center"><bold>mice (C57BL/6)</bold> m/f, aged</td>
<td valign="top" align="center"><bold>novelty</bold> 3 h <italic>(fed)</italic></td>
<td valign="top" align="center">&#x2193; <bold>m</bold> vs. &#x2194; <bold>f</bold></td>
<td valign="top" align="center">@ 6 h, 24 h <italic>FI cumul</italic></td>
<td valign="top" align="center">-</td>
<td valign="top" align="center">-</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B219">Stengel et al., 2010</xref>)</td>
<td valign="top" align="center"><bold>rats (SPD)</bold> m</td>
<td valign="top" align="center"><bold>LPS injection</bold> 100 &#x03BC;g/kg (<italic>fasted, 16h)</italic></td>
<td valign="top" align="center">&#x2193;</td>
<td valign="top" align="center">@ 2 h, 5 h, 7 h, 24 h <italic>FI per time period</italic></td>
<td valign="top" align="center">-</td>
<td valign="top" align="center">-</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="center" colspan="7"><bold>(Sub)chronic stress paradigms</bold></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B98">Jeong et al., 2013</xref>)</td>
<td valign="top" align="center"><bold>mice (ICR)</bold> m</td>
<td valign="top" align="center"><bold>immobilization stress</bold> 2 h/d, 15 d</td>
<td valign="top" align="center">&#x2193; \ (&#x2193;)<sup><italic>ns</italic></sup></td>
<td valign="top" align="center">@ 2 d-6 d \ 7 d-15 d <italic>FI daily</italic></td>
<td valign="top" align="center">&#x2194;</td>
<td valign="top" align="center">@ 2 d-15 d <italic>BW g</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B103">Jiang and Eiden, 2016</xref>)</td>
<td valign="top" align="center"><bold>mice (PACAP WT)</bold> m, C57BL/6N bckg</td>
<td valign="top" align="center"><bold>immobilization stress</bold> 1 h/d, 7 d</td>
<td valign="top" align="center">&#x2193;</td>
<td valign="top" align="center">@ 7 d <italic>FI cumul</italic></td>
<td valign="top" align="center">&#x2193;</td>
<td valign="top" align="center">@ 7 d <italic>BW loss %</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B134">Li et al., 2015</xref>)</td>
<td valign="top" align="center"><bold>mice (ICR)</bold> f, maternal</td>
<td valign="top" align="center"><bold>immobilization stress</bold> ? h/d, 21 d</td>
<td valign="top" align="center">(&#x2193;)<sup><italic>ns</italic></sup></td>
<td valign="top" align="center">@ 1 d-16 d <italic>FI daily</italic></td>
<td valign="top" align="center">&#x2193;</td>
<td valign="top" align="center">@ 3 d-16 d <italic>BW g</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B156">Mograbi et al., 2020</xref>)</td>
<td valign="top" align="center"><bold>rats (WST)</bold> m</td>
<td valign="top" align="center"><bold>immobilization stress</bold> 2,4 or 6 h/d, 21 d</td>
<td valign="top" align="center">-</td>
<td valign="top" align="center">-</td>
<td valign="top" align="center">&#x2193;</td>
<td valign="top" align="center">@ 1 w, 2 w, 3 w <italic>BW gain %</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B165">Ochi et al., 2008</xref>)</td>
<td valign="top" align="center"><bold>rats (WST)</bold> m</td>
<td valign="top" align="center"><bold>water cage</bold> 5 d</td>
<td valign="top" align="center">-</td>
<td valign="top" align="center">-</td>
<td valign="top" align="center">&#x2193;</td>
<td valign="top" align="center">@ d1-d5 <italic>BW change %</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">4&#x002A;(<xref ref-type="bibr" rid="B95">Izadi et al., 2018</xref>)</td>
<td valign="top" align="center"><bold>rats (WST)</bold> m</td>
<td valign="top" align="center"><bold>social stress</bold> 7 d</td>
<td valign="top" align="center">&#x2194;</td>
<td valign="top" align="center">@ 8 d <italic>FI cumul (3 h)</italic></td>
<td valign="top" align="center">&#x2194;</td>
<td valign="top" align="center">@ 7 d <italic>BW change g</italic></td>
</tr>
<tr>
<td/>
<td valign="top" align="left" colspan="6"><hr/></td>
</tr>
<tr>
<td/>
<td valign="top" align="center"><bold>rats (WST)</bold> m</td>
<td valign="top" align="center"><bold>social isolation</bold> 7 d</td>
<td valign="top" align="center">&#x2193;</td>
<td valign="top" align="center">@ 8 d <italic>FI cumul (3 h)</italic></td>
<td valign="top" align="center">&#x2193;</td>
<td valign="top" align="center">@ 7 d <italic>BW change g</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B189">Rostamkhani et al., 2016</xref>)</td>
<td valign="top" align="center"><bold>rats (WST)</bold> m</td>
<td valign="top" align="center"><bold>foot shock</bold> 60 &#x00D7; 10 s, 15 d</td>
<td valign="top" align="center">&#x2194; \ &#x2193; \ (&#x2193;)<sup><italic>ns</italic></sup></td>
<td valign="top" align="center">@ 2 d \ 7 d \ 15 d <italic>FI cumul (24 h)</italic></td>
<td valign="top" align="center">&#x2194; \ &#x2193;</td>
<td valign="top" align="center">@ d1 \ d15 <italic>BW g</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B237">Yam et al., 2017</xref>)</td>
<td valign="top" align="center"><bold>mice (C57BL/6J)</bold> m/f, pups (p2-p14)</td>
<td valign="top" align="center"><bold>early chronic stress</bold> 7 d (p2-p9)</td>
<td valign="top" align="center">-</td>
<td valign="top" align="center">-</td>
<td valign="top" align="center">&#x2193; \ &#x2191;</td>
<td valign="top" align="center">@ p2-p9 \ p9-p14 <italic>BW gain g</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B54">Elbassuoni, 2014</xref>)</td>
<td valign="top" align="center"><bold>rats (SPD)</bold> m/f</td>
<td valign="top" align="center"><bold>immobilization stress</bold> 20 min/d, 21 d</td>
<td valign="top" align="center">&#x2191; (<bold>m</bold> &#x003E; <bold>f</bold>)</td>
<td valign="top" align="center">@ 1 d-21 d <italic>FI daily avgd</italic></td>
<td valign="top" align="center">&#x2191; (<bold>m</bold> &#x003E; <bold>f</bold>)</td>
<td valign="top" align="center">@ 21d <italic>BW gain g</italic></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B172">Patterson et al., 2010</xref>)</td>
<td valign="top" align="center"><bold>mice (GHSR WT/KO)</bold> m, C57BL/6J-DBA bckg</td>
<td valign="top" align="center"><bold>CUMS</bold> 14 d <italic>(STD</italic> + <italic>HFD)</italic></td>
<td valign="top" align="center">&#x2193; &#x2194; <bold>GHSR-KO</bold></td>
<td valign="top" align="center">@ 1 d-14 d <italic>kcal daily avgd</italic></td>
<td valign="top" align="center">&#x2193; &#x2194; <bold>GHSR-KO</bold></td>
<td valign="top" align="center">@ d14 <italic>BW change g</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B241">Yao et al., 2016</xref>)</td>
<td valign="top" align="center"><bold>mice (C57BL/6N)</bold> m</td>
<td valign="top" align="center"><bold>CUMS + social isolation</bold> 21 d <italic>(fasted, 12 h)</italic></td>
<td valign="top" align="center">&#x2193;</td>
<td valign="top" align="center">@ 21 d <italic>FI cumul (24 h)/BW</italic></td>
<td valign="top" align="center">-</td>
<td valign="top" align="center">-</td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B83">He et al., 2018</xref>)</td>
<td valign="top" align="center"><bold>rats (SPD)</bold> f</td>
<td valign="top" align="center"><bold>CUMS</bold> 4 w</td>
<td valign="top" align="center">-</td>
<td valign="top" align="center">-</td>
<td valign="top" align="center">&#x2193;</td>
<td valign="top" align="center">@ 1 w, 2 w, 3 w, 4 w <italic>BW change %</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B239">Yan et al., 2018</xref>)</td>
<td valign="top" align="center"><bold>mice (C57BL/6J)</bold> m</td>
<td valign="top" align="center"><bold>CUMS</bold> 21 d</td>
<td valign="top" align="center">&#x2194; \ &#x2193;</td>
<td valign="top" align="center">@ 7 d, 14 d \ 21 d <italic>FI cumul (24 h) ?</italic></td>
<td valign="top" align="center">&#x2194; \ &#x2193;</td>
<td valign="top" align="center">@ 7 d, 14 d \ 21 d <italic>BW g</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B59">Forbes et al., 1996</xref>)</td>
<td valign="top" align="center"><bold>rats (LH)</bold> m</td>
<td valign="top" align="center"><bold>CUMS</bold> 6 w</td>
<td valign="top" align="center">-</td>
<td valign="top" align="center">-</td>
<td valign="top" align="center">&#x2193;</td>
<td valign="top" align="center">@ 1 w-6 w <italic>BW g</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B81">Harris et al., 1997</xref>)</td>
<td valign="top" align="center"><bold>rats (WST)</bold> m</td>
<td valign="top" align="center"><bold>CUMS</bold> 40 d</td>
<td valign="top" align="center">&#x2194;</td>
<td valign="top" align="center">@ 1 d-40 d <italic>FI daily</italic></td>
<td valign="top" align="center">&#x2194; \ &#x2193;</td>
<td valign="top" align="center">@ 1 d-3 d \ 4 d-40 d <italic>BW g</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B138">Lopez Lopez et al., 2018</xref>)</td>
<td valign="top" align="center"><bold>rats (WST)</bold> m</td>
<td valign="top" align="center"><bold>CUMS</bold> 60 d</td>
<td valign="top" align="center">&#x2194;</td>
<td valign="top" align="center">@ 1 d-60 d <italic>FI daily</italic></td>
<td valign="top" align="center">&#x2194; \ &#x2193;</td>
<td valign="top" align="center">@ 1 d-40 d \ 40 d-60 d <italic>BW g</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">8&#x002A;(<xref ref-type="bibr" rid="B207">Simas et al., 2018</xref>)</td>
<td valign="top" align="center"><bold>rats (WST)</bold> m</td>
<td valign="top" align="center"><bold>CUMS</bold> 4 w <italic>(STD)</italic></td>
<td valign="top" align="center">&#x2194;</td>
<td valign="top" align="center">@ 1 w, 2 w, 3 w, 4 w <italic>FI daily avgd</italic></td>
<td valign="top" align="center">&#x2194; (but no BW gain from 0w as control)</td>
<td valign="top" align="center">@ 1 w, 2 w, 3 w, 4 w <italic>BW g</italic></td>
</tr>
<tr>
<td/>
<td valign="top" align="left" colspan="6"><hr/></td>
</tr>
<tr>
<td/>
<td valign="top" align="justify"/>
<td valign="top" align="center"><bold>CUMS</bold> 4 w <italic>(HFD)</italic></td>
<td valign="top" align="center">&#x2194; \ &#x2193; \ (&#x2193;)<sup><italic>ns</italic></sup></td>
<td valign="top" align="center">@ 1 w, 2 w \ 3 w \ 4 w <italic>FI daily avgd</italic></td>
<td valign="top" align="center">&#x2194; \ &#x2193;</td>
<td valign="top" align="center">@ 1 w, 2 w, 3 w \ 4 w <italic>BW g</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B136">Li et al., 2019</xref>)</td>
<td valign="top" align="center"><bold>rats (WST)</bold> m</td>
<td valign="top" align="center"><bold>CUMS</bold> 4 w</td>
<td valign="top" align="center">-</td>
<td valign="top" align="center">-</td>
<td valign="top" align="center">&#x2194; \ &#x2193; (and &#x2193; BW gain from 1 w)</td>
<td valign="top" align="center">@ 1 w \ 2 w, 3 w, 4 w <italic>BW g</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B244">Yun et al., 2020</xref>)</td>
<td valign="top" align="center"><bold>mice (C57BL/6N)</bold> m</td>
<td valign="top" align="center"><bold>CUMS</bold> 6 w</td>
<td valign="top" align="center">-</td>
<td valign="top" align="center">-</td>
<td valign="top" align="center">&#x2194; \ &#x2193;</td>
<td valign="top" align="center">@ 2 w \ 4 w, 6 w <italic>BW change g</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B92">Huang et al., 2017</xref>)</td>
<td valign="top" align="center"><bold>mice (C57BL/6J)</bold> m</td>
<td valign="top" align="center"><bold>CUMS</bold> 8 w</td>
<td valign="top" align="center">&#x2191;</td>
<td valign="top" align="center">@ 0 w-8 w <italic>(1x/w) FI daily avgd</italic></td>
<td valign="top" align="center">&#x2194;</td>
<td valign="top" align="center">@ 8 w <italic>BW change g</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B142">Lutter et al., 2008</xref>)</td>
<td valign="top" align="center"><bold>mice (GHSR WT/KO)</bold> m, C57BL/6 J bckg</td>
<td valign="top" align="center"><bold>CSDS</bold> 10 d</td>
<td valign="top" align="center">&#x2191; &#x2194; <bold>GHSR KO</bold></td>
<td valign="top" align="center">@ 1 d-10 d, 11 d-13 d <italic>FI daily avgd</italic></td>
<td valign="top" align="center">&#x2194;</td>
<td valign="top" align="center">@ 1 d-13 d <italic>BW change g</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">5&#x002A;(<xref ref-type="bibr" rid="B173">Patterson et al., 2013a</xref>)</td>
<td valign="top" align="center"><bold>mice (C57BL/6J)</bold> m</td>
<td valign="top" align="center"><bold>CSDS</bold> 21 d <italic>(STD</italic> + <italic>HFD 4h/d)</italic></td>
<td valign="top" align="center">&#x2191; <bold>STD</bold> vs. &#x2193; <bold>HFD</bold></td>
<td valign="top" align="center">@ 1 d-21 d <italic>FI daily avgd</italic></td>
<td valign="top" align="center"><italic>&#x2191;</italic></td>
<td valign="top" align="center">@ 1 d-21 d <italic>BW g avgd</italic></td>
</tr>
<tr>
<td/>
<td valign="top" align="left" colspan="6"><hr/></td>
</tr>
<tr>
<td/>
<td valign="top" align="center"><bold>mice (GHSR WT/KO)</bold> m, C57BL/6J bckg</td>
<td valign="top" align="center"><bold>CSDS</bold> 21 d <italic>(STD</italic> + <italic>HFD 4h/d)</italic></td>
<td valign="top" align="center">&#x2191; &#x2194; <bold>GHSR KO</bold></td>
<td valign="top" align="center">@ 1 d-21 d <italic>kcal daily avgd</italic></td>
<td valign="top" align="center"><italic>&#x2191;</italic> &#x2194; <bold>GHSR KO</bold></td>
<td valign="top" align="center">@ 21 d <italic>BW gain g</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B174">Patterson et al., 2013b</xref>)</td>
<td valign="top" align="center"><bold>mice (C57BL/6J)</bold> m</td>
<td valign="top" align="center"><bold>CSDS</bold> 21 d</td>
<td valign="top" align="center">&#x2191;</td>
<td valign="top" align="center">@ 1 d-21 d <italic>FI and kcal daily avgd</italic></td>
<td valign="top" align="center">&#x2194;</td>
<td valign="top" align="center">@ 21 d <italic>BW, BW change g</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">5&#x002A;(<xref ref-type="bibr" rid="B185">Razzoli et al., 2015</xref>)</td>
<td valign="top" align="center"><bold>mice (C57BL/6J)</bold> m</td>
<td valign="top" align="center"><bold>CSDS</bold> 4 w</td>
<td valign="top" align="center">&#x2191;</td>
<td valign="top" align="center">@ 1 w-4 w ? <italic>FI daily avgd</italic></td>
<td valign="top" align="center">-</td>
<td valign="top" align="center">-</td>
</tr>
<tr>
<td/>
<td valign="top" align="center"><bold>mice (CD1)</bold> m</td>
<td valign="top" align="center"><bold>CSDS</bold> 4 w <italic>(STD 1 w</italic>, <italic>HFD 3 w)</italic></td>
<td valign="top" align="center">&#x2191; \ &#x2194;</td>
<td valign="top" align="center">@ 1 w, 2 w, 3 w \ 4 w <italic>kcal daily avgd ?</italic></td>
<td valign="top" align="center">&#x2194; \ &#x2191;</td>
<td valign="top" align="center">@ 1 w \ 2 w, 3 w, 4 w <italic>BW g</italic></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B35">Chuang et al., 2011</xref>)</td>
<td valign="top" align="center"><bold>mice (GHSR WT/KO)</bold> m, C57BL/6J bckg</td>
<td valign="top" align="center"><bold>CSDS</bold> 10 d</td>
<td valign="top" align="center"><bold>STD</bold> &#x2194; vs. <bold>HFD</bold> &#x2191;&#x2194; <bold>GHSR KO</bold></td>
<td valign="top" align="center">@ 26 d (during CPP) <italic>FI cumul (CPP)</italic></td>
<td valign="top" align="center"><italic>&#x2191;</italic> &#x2194; <bold>GHSR KO</bold></td>
<td valign="top" align="center">@ 26 d (during CPP) <italic>BW change % (CPP)</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B21">Berton et al., 1998</xref>)</td>
<td valign="top" align="center"><bold>rats (LEW)</bold> m</td>
<td valign="top" align="center"><bold>RI SDS</bold> 7 d</td>
<td valign="top" align="center">&#x2193; \ (&#x2193;)<sup><italic>ns</italic></sup></td>
<td valign="top" align="center">@ 1 d-5 d \ 6 d-7 d <italic>FI daily (g/100g)</italic></td>
<td valign="top" align="center">&#x2193; \ &#x2194;</td>
<td valign="top" align="center">@ 1 d-4 d \ 5 d-6 d <italic>BW change %</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B56">Fanous et al., 2011</xref>)</td>
<td valign="top" align="center"><bold>rats (SPD)</bold> m</td>
<td valign="top" align="center"><bold>RI SDS</bold> every 3 d, 10 d</td>
<td valign="top" align="center">-</td>
<td valign="top" align="center">-</td>
<td valign="top" align="center">&#x2193;</td>
<td valign="top" align="center">@ 10 d <italic>BW gain g</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="7"><hr/></td>
</tr>
<tr>
<td valign="top" align="left">(<xref ref-type="bibr" rid="B171">Patki et al., 2013</xref>)</td>
<td valign="top" align="center"><bold>rats (SPD)</bold> m</td>
<td valign="top" align="center"><bold>RI SDS</bold> 7 d</td>
<td valign="top" align="center">&#x2194;</td>
<td valign="top" align="center">@ 1 d-7 d <italic>FI daily avgd</italic></td>
<td valign="top" align="center">&#x2193;</td>
<td valign="top" align="center">@ 7 d <italic>BW gain g</italic></td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<attrib><italic>Acute paradigms: Measurements after stressor cessation (@ x h/d/w; 1 = start of stressor). Chronic paradigms: Measurements during paradigm and/or after stressor cessation as indicated (@ x h/d). Abbreviations: TMDS3, Tryon Maze Dull S3; WST, Wistar; SPD, Sprague-Dawley; bckg, background; p, postnatal day; LH, Lister hooded; LEW, Lewis; LPS, lipopolysaccharide; CUMS, chronic mild unpredictable stress; STD, standard diet; HFD, high-fat diet; CSDS, chronic social defeat stress; RI, resident-intruder; SDS, social defeat stress; FI, food intake; cumul, cumulative; avgd, averaged; BW, body weight; ()<sup><italic>ns</italic></sup>, non-significant.</italic></attrib>
</table-wrap-foot>
</table-wrap>
<p>Acute stressors such as a single session of social defeat (<xref ref-type="bibr" rid="B151">Meerlo et al., 1996</xref>), immobilization stress (<xref ref-type="bibr" rid="B70">Gul et al., 2017</xref>), novelty stress (<xref ref-type="bibr" rid="B192">Saegusa et al., 2011</xref>; <xref ref-type="bibr" rid="B146">Matsumoto et al., 2017</xref>) but also LPS injection (<xref ref-type="bibr" rid="B219">Stengel et al., 2010</xref>) were mostly found to reduce food intake. While only a few of these studies measured body weight, they reported a decrease following exposure to an acute stressor (<xref ref-type="bibr" rid="B151">Meerlo et al., 1996</xref>; <xref ref-type="bibr" rid="B70">Gul et al., 2017</xref>).</p>
<p>Also in subchronic and chronic stress paradigms food intake and body weight are typically negatively affected. For example, repeated immobilization stress decreased food intake (<xref ref-type="bibr" rid="B98">Jeong et al., 2013</xref>; <xref ref-type="bibr" rid="B103">Jiang and Eiden, 2016</xref>) and in parallel decreased (<xref ref-type="bibr" rid="B134">Li et al., 2015</xref>; <xref ref-type="bibr" rid="B103">Jiang and Eiden, 2016</xref>; <xref ref-type="bibr" rid="B156">Mograbi et al., 2020</xref>) or had no effect on body weight (<xref ref-type="bibr" rid="B98">Jeong et al., 2013</xref>). Also exposure to a flooded cage for five days decreased body weight (<xref ref-type="bibr" rid="B165">Ochi et al., 2008</xref>) and, similarly, social isolation for a week (<xref ref-type="bibr" rid="B95">Izadi et al., 2018</xref>) or chronic administration of foot shocks (<xref ref-type="bibr" rid="B189">Rostamkhani et al., 2016</xref>) reduced food intake and body weight. Early life stress induced by limited access to bedding and nesting material for a week led to attenuated weight gain during stress exposure in male and female pups, which was compensated by an increased weight gain after termination of the stress exposure (<xref ref-type="bibr" rid="B237">Yam et al., 2017</xref>). As an exception, only one study found increased food intake and body weight gain during immobilization stress over a period of three weeks, which was more pronounced in male than female rats (<xref ref-type="bibr" rid="B54">Elbassuoni, 2014</xref>).</p>
<p>Exposure to CUMS, which utilizes a battery of different stressors over a time course of several weeks, relatively consistently led to decreases in food intake (<xref ref-type="bibr" rid="B172">Patterson et al., 2010</xref>; <xref ref-type="bibr" rid="B241">Yao et al., 2016</xref>; <xref ref-type="bibr" rid="B83">He et al., 2018</xref>; <xref ref-type="bibr" rid="B239">Yan et al., 2018</xref>) and body weight in mice and rats (<xref ref-type="bibr" rid="B59">Forbes et al., 1996</xref>; <xref ref-type="bibr" rid="B81">Harris et al., 1997</xref>; <xref ref-type="bibr" rid="B172">Patterson et al., 2010</xref>; <xref ref-type="bibr" rid="B138">Lopez Lopez et al., 2018</xref>; <xref ref-type="bibr" rid="B207">Simas et al., 2018</xref>; <xref ref-type="bibr" rid="B239">Yan et al., 2018</xref>; <xref ref-type="bibr" rid="B136">Li et al., 2019</xref>; <xref ref-type="bibr" rid="B244">Yun et al., 2020</xref>). A few studies reported decreases in body weight or body weight gain, while food intake was not significantly altered (<xref ref-type="bibr" rid="B81">Harris et al., 1997</xref>; <xref ref-type="bibr" rid="B138">Lopez Lopez et al., 2018</xref>; <xref ref-type="bibr" rid="B207">Simas et al., 2018</xref>). Only one study found an increase in daily chow consumption and no differences in body weight between CUMS and non-CUMS mice after eight weeks of stress exposure (<xref ref-type="bibr" rid="B92">Huang et al., 2017</xref>). Interestingly, Simas et al. reported a decreased food intake in mice exposed to CUMS compared to non-stressed mice when only a high-fat diet (HFD) was provided, but not when fed a standard diet (<xref ref-type="bibr" rid="B207">Simas et al., 2018</xref>). This suggests that the rewarding properties of calorically dense food are abolished during CUMS. In line with this notion, several of the previously mentioned studies also evaluated sucrose or saccharine preference. Some found no differences (<xref ref-type="bibr" rid="B59">Forbes et al., 1996</xref>; <xref ref-type="bibr" rid="B81">Harris et al., 1997</xref>; <xref ref-type="bibr" rid="B244">Yun et al., 2020</xref>), but in several studies CUMS exposure led to reduced sucrose or saccharine intake (<xref ref-type="bibr" rid="B241">Yao et al., 2016</xref>; <xref ref-type="bibr" rid="B92">Huang et al., 2017</xref>; <xref ref-type="bibr" rid="B83">He et al., 2018</xref>; <xref ref-type="bibr" rid="B239">Yan et al., 2018</xref>), which may reflect stress-induced anhedonia.</p>
<p>On the other hand, CSDS in mice quite robustly led to increases in food intake (<xref ref-type="bibr" rid="B142">Lutter et al., 2008</xref>; <xref ref-type="bibr" rid="B173">Patterson et al., 2013a</xref>, <xref ref-type="bibr" rid="B174">b</xref>; <xref ref-type="bibr" rid="B185">Razzoli et al., 2015</xref>), associated with an increase in body weight in some studies (<xref ref-type="bibr" rid="B173">Patterson et al., 2013a</xref>; <xref ref-type="bibr" rid="B185">Razzoli et al., 2015</xref>) but not in others (<xref ref-type="bibr" rid="B142">Lutter et al., 2008</xref>; <xref ref-type="bibr" rid="B174">Patterson et al., 2013b</xref>). Chuang and colleagues showed that conditioned place preference (CPP) for HFD was significantly increased in CSDS-exposed mice, which was associated with a higher intake of HFD chow and a greater weight gain over the course of the CPP paradigm (<xref ref-type="bibr" rid="B35">Chuang et al., 2011</xref>). However, in contrast to these studies in mice, subchronic and chronic social defeat paradigms in rats resulted in decreases in daily food intake (<xref ref-type="bibr" rid="B21">Berton et al., 1998</xref>) and body weight (<xref ref-type="bibr" rid="B21">Berton et al., 1998</xref>; <xref ref-type="bibr" rid="B56">Fanous et al., 2011</xref>; <xref ref-type="bibr" rid="B171">Patki et al., 2013</xref>).</p>
<p>Some of the aforementioned studies also investigated the role of the GHSR in stress-related changes in feeding behavior and found that both increases (CSDS) or decreases (CUMS) in food intake and body weight gain were abolished in GHSR KO mice (<xref ref-type="bibr" rid="B142">Lutter et al., 2008</xref>; <xref ref-type="bibr" rid="B172">Patterson et al., 2010</xref>, <xref ref-type="bibr" rid="B173">2013a</xref>). Moreover, increased CPP for and higher intake of HFD and an associated weight gain after CSDS exposure were not present in GHSR KO mice (<xref ref-type="bibr" rid="B35">Chuang et al., 2011</xref>), indicating a central role of ghrelin signaling in these stress-induced changes. The increased CPP, however, could be reinstated by selective re-expression of GHSR in tyrosine hydroxylase-positive neurons, which the authors concluded are very likely involved in mediating stress-induced food reward. Interestingly, a recent study used re-expression of GHSR in dopamine transporter (DAT)-positive neurons of GHSR KO mice to confirm that GHSR signaling in dopaminergic neurons controls appetitive and consummatory behaviors toward HFD in <italic>ad libitum</italic> fed mice (<xref ref-type="bibr" rid="B37">Cornejo et al., 2020</xref>). Indeed, it has been proposed previously that the ghrelin system may play an important role in stress-induced food reward behavior and act as a critical modulator at the interface of homeostatic control of appetite and food reward during stress, promoting hyperphagia and hedonic intake of calorically dense &#x2018;comfort foods&#x2019; (<xref ref-type="bibr" rid="B200">Schellekens et al., 2012</xref>).</p>
<p>Even though stress paradigms typically increase AG levels and in some instances increase feeding, paradoxically, exposure to stress may also be associated with a decrease in food intake and body weight. During acute stress exposure, it is likely that the orexigenic effects of high plasma AG are overcome by other factors, such as stress-induced changes in CRF signaling in the brain (<xref ref-type="bibr" rid="B105">Jochman et al., 2005</xref>; <xref ref-type="bibr" rid="B79">Haque et al., 2013</xref>; <xref ref-type="bibr" rid="B51">Dunn et al., 2015</xref>; <xref ref-type="bibr" rid="B155">Mogami et al., 2016</xref>). Chronic stress, on the other hand, might induce central ghrelin resistance, associated with lower GHSR expression in particular brain areas (<xref ref-type="bibr" rid="B80">Harmatz et al., 2016</xref>), which then may further contribute to reduced food intake and anhedonia-like behaviors in a GHSR-dependent manner, but irrespective of high circulating AG concentrations. This may apply for physical stressors like foot shocks, immobilization stress or various stressors used during CUMS which are typically associated with reduced food intake and decreases in body weight. The same hypothesis, however, does not seem to hold true for CSDS in mice, where high plasma AG is mostly associated with increases in food intake and where GHSR signaling in dopaminergic neurons has been proposed to mediate stress-induced food reward as a coping mechanism (<xref ref-type="bibr" rid="B35">Chuang et al., 2011</xref>). The observation that CSDS increases food intake and/or body weight specifically in mice but not in rats could be attributed to species differences in social dominance behavior (<xref ref-type="bibr" rid="B122">Kondrakiewicz et al., 2019</xref>). The question remains what impact circulating ghrelin and central GHSR signaling may have on other stress-related behaviors in rodents.</p>
</sec>
<sec id="S2.SS3">
<title>Role of Circulating Ghrelin in Fear, Anxiety- and Depression-Like Behaviors</title>
<p>While some studies propose that ghrelin reduces fear, anxiety- and depression-like behaviors in rodents, others actually suggest an opposite role. One early study showed that central administration of ghrelin antisense DNA had anxiolytic and antidepressant-like effects and reduced the retrieval of conditioned fear in unstressed rats (<xref ref-type="bibr" rid="B109">Kanehisa et al., 2006</xref>). Similarly, Spencer and colleagues found reduced anxiety-like behaviors in ghrelin KO mice under baseline conditions, but increased anxiety scores following acute immobilization stress (<xref ref-type="bibr" rid="B217">Spencer et al., 2012</xref>). However, a more recent study also found higher anxiety-like behavior in ghrelin KO mice under non-stressed conditions (<xref ref-type="bibr" rid="B143">Mahbod et al., 2018</xref>). A genetic deletion of GOAT and thus attenuated AG levels (<xref ref-type="bibr" rid="B245">Zhao et al., 2010</xref>) reduced anxiety-like behavior prior to stress exposure (<xref ref-type="bibr" rid="B143">Mahbod et al., 2018</xref>) or was anxiogenic regardless of stress conditions (<xref ref-type="bibr" rid="B218">Stark et al., 2016</xref>).</p>
<p>Pharmacological studies investigating the effects of AG and other GHSR ligands have also delivered contradictory results. Systemic or central injection of a single dose of AG has been shown to induce anxiety- and depression-like behaviors in mice and rats that were not previously subjected to stress (<xref ref-type="bibr" rid="B12">Asakawa et al., 2001a</xref>; <xref ref-type="bibr" rid="B31">Carlini et al., 2002</xref>, <xref ref-type="bibr" rid="B32">2004</xref>; <xref ref-type="bibr" rid="B43">Currie et al., 2012</xref>, <xref ref-type="bibr" rid="B44">2014</xref>; <xref ref-type="bibr" rid="B25">Brockway et al., 2016</xref>; <xref ref-type="bibr" rid="B96">Jackson et al., 2019</xref>). Similarly, central infusion of ghrelin for one month increased anxiety- and depression-like behavior in rats (<xref ref-type="bibr" rid="B78">Hansson et al., 2011</xref>). In contrast, a few other studies reported anxiolytic and antidepressant-like effects of a single systemic dose of AG in non-stressed mice (<xref ref-type="bibr" rid="B142">Lutter et al., 2008</xref>; <xref ref-type="bibr" rid="B97">Jensen et al., 2016</xref>). In a recent publication, the administration of AG into the dorsal raphe nucleus was anxiolytic in an inhibitory avoidance test but facilitated learned escape behavior in rats (<xref ref-type="bibr" rid="B33">Cavalcante et al., 2019</xref>).</p>
<p>In studies where AG is administered systemically, it should generally be considered that it can be converted to DAG (<xref ref-type="bibr" rid="B48">De Vriese et al., 2004</xref>). This could be relevant, given that DAG was found to have anxiogenic effects in ghrelin KO mice which were not previously subjected to stress (<xref ref-type="bibr" rid="B218">Stark et al., 2016</xref>). Moreover, the effects of exogenous AG administration may also depend on feeding state. An injection of ghrelin into the amygdala had no significant effect in fed mice, but was anxiolytic when no food was available (<xref ref-type="bibr" rid="B9">Alvarez-Crespo et al., 2012</xref>), suggesting that AG may promote foraging and risk-taking in response to a negative energy balance.</p>
<p>When focusing on the effects of exogenously administered ghrelin following stress exposure, an anxiolytic effect appears more evident. Peripherally administered AG attenuated anxiety-like behavior and stress responses after exposure to air puffs or immobilization stress (<xref ref-type="bibr" rid="B97">Jensen et al., 2016</xref>). Interestingly, DAG also produced anxiolytic-like effects following stress exposure in ghrelin KO mice (<xref ref-type="bibr" rid="B218">Stark et al., 2016</xref>). Moreover, anxiety- and depression-like behaviors induced by CUMS were at least partly rescued by administration of ghrelin or the ghrelin agonist GHRP-6 (<xref ref-type="bibr" rid="B92">Huang et al., 2017</xref>, <xref ref-type="bibr" rid="B91">2019</xref>). A recent study demonstrated that intra-hippocampal administration of ghrelin fully and intraperitoneal injection partly normalized stress-enhanced anxiety- and depression-like phenotypes in a CSDS paradigm (<xref ref-type="bibr" rid="B75">Han et al., 2019</xref>). However, another study found that reduced social interaction following CSDS exposure could not be rescued by subcutaneous administration of AG or ghrelin agonist GHRP-2 (<xref ref-type="bibr" rid="B72">Gupta et al., 2019</xref>).</p>
<p>A number of studies also investigated how GHSR ligands affect fear conditioning and extinction. Administration of the GHSR agonist MK0677, systemically or directly into the basolateral amygdala, around the time of fear conditioning reduced contextual and cued fear memory strength in unstressed rats, while the GHSR antagonist D-Lys3 increased it (<xref ref-type="bibr" rid="B80">Harmatz et al., 2016</xref>). An earlier study of the same group, however, showed that repeated systemic or intra-amygdalar injection of MK0677 led to an enhancement of cued fear memory strength (<xref ref-type="bibr" rid="B153">Meyer et al., 2014</xref>). In rats that were subjected to chronic immobilization stress, stress-induced increases in cued fear were abolished when the GHSR antagonist D-Lys3-GHRP-6 was administered daily before stress exposure (<xref ref-type="bibr" rid="B153">Meyer et al., 2014</xref>). In their 2016 study, this group reported that increased cued fear in chronically stress-exposed rats was associated with reduced binding of fluorescently labeled ghrelin in the basolateral amygdala, which they defined as central ghrelin resistance (<xref ref-type="bibr" rid="B80">Harmatz et al., 2016</xref>). Therefore, the authors hypothesized that a stress-induced elevation of AG levels and prolonged GHSR activation may lead to impaired GHSR signaling in the brain via downregulation of GHSR expression (<xref ref-type="bibr" rid="B80">Harmatz et al., 2016</xref>). Interestingly, infusion of MK0677 into the lateral amygdala was also shown to improve cued fear extinction in non-stressed mice (<xref ref-type="bibr" rid="B90">Huang et al., 2016</xref>). However, in our recently published study, we did not find significant effects of systemic or intra-VTA administration of MK0677 on cued fear expression or extinction in non-stressed mice (<xref ref-type="bibr" rid="B179">Pierre et al., 2020</xref>). Importantly, as the GHSR is constitutively active in the absence of ghrelin (<xref ref-type="bibr" rid="B87">Holst et al., 2003</xref>; <xref ref-type="bibr" rid="B177">Petersen et al., 2009</xref>), it is therefore important to consider the effects of central GHSR signaling independently of circulating AG or exogenous administration of an GHSR agonist.</p>
</sec>
<sec id="S2.SS4">
<title>Role of GHSR Signaling in Fear, Anxiety- and Depression-Like Behaviors</title>
<p>Under non-stressed conditions, no or only marginal effects on fear, anxiety- and depression like behaviors were observed in GHSR KO mice compared to wild type controls (<xref ref-type="bibr" rid="B143">Mahbod et al., 2018</xref>; <xref ref-type="bibr" rid="B71">Guo et al., 2019</xref>; <xref ref-type="bibr" rid="B140">Lu et al., 2019</xref>; <xref ref-type="bibr" rid="B178">Pierre et al., 2019</xref>). Nevertheless, one study found anxiolytic and antidepressant-like effects following overexpression of GHSR in the basolateral amygdala in non-stressed mice (<xref ref-type="bibr" rid="B97">Jensen et al., 2016</xref>). Another study reported reduced fear memory retention after contextual fear conditioning in unstressed GHSR KO mice (<xref ref-type="bibr" rid="B7">Albarran-Zeckler et al., 2012</xref>), but this observation was not confirmed in a more recent study (<xref ref-type="bibr" rid="B88">Hornsby et al., 2016</xref>).</p>
<p>Clearer evidence for behavioral effects in mice lacking the GHSR was obtained following stress exposure, where most studies reported impaired stress coping. For example, mild stressors like air puffs induced an exacerbated avoidance response in GHSR KO mice (<xref ref-type="bibr" rid="B97">Jensen et al., 2016</xref>). Similarly, CSDS resulted in more pronounced depression-like behavior in GHSR KO mice, as assessed by a social avoidance test (<xref ref-type="bibr" rid="B142">Lutter et al., 2008</xref>; <xref ref-type="bibr" rid="B35">Chuang et al., 2011</xref>). A local knockdown of the GHSR in the hippocampus also aggravated anxiety- and depression-like behaviors in mice following exposure to a CSDS or CUMS paradigm (<xref ref-type="bibr" rid="B75">Han et al., 2019</xref>; <xref ref-type="bibr" rid="B91">Huang et al., 2019</xref>), pointing to a protective role of the GHSR during chronic stress.</p>
</sec>
<sec id="S2.SS5">
<title>Effects of Caloric Restriction on Fear, Anxiety- and Depression-Like Behaviors</title>
<p>Caloric restriction and food deprivation paradigms typically increase plasma ghrelin levels and were also used in several studies to manipulate the endogenous ghrelin system and thus indirectly study its effects on fear, anxiety- and depression-related behaviors in rodents. An initial study demonstrated anxiolytic and antidepressant-like effects of caloric restriction that were abolished in GHSR KO mice (<xref ref-type="bibr" rid="B142">Lutter et al., 2008</xref>). In a later publication, the same group showed that the neuroprotective agent P7C3 restored the antidepressant-like effect of caloric restriction in GHSR KO mice, potentially by increasing hippocampal neurogenesis (<xref ref-type="bibr" rid="B229">Walker et al., 2015</xref>). This suggests that the effects of caloric restriction on depression-like behaviors may depend on GHSR signaling in the hippocampus and ensuing neurogenesis. Recently, a study reported that acute food deprivation for 24 h and chronic caloric restriction had anxiolytic- and antidepressant-like effects in wild type mice, which were abolished after re-feeding (<xref ref-type="bibr" rid="B140">Lu et al., 2019</xref>). In GHSR-KO mice, however, acute food deprivation enhanced, while only chronic caloric restriction reduced anxiety- and depression-like responses. This led the authors to conclude that the positive effect of acute but not chronic fasting was GHSR-dependent (<xref ref-type="bibr" rid="B140">Lu et al., 2019</xref>). The finding that the anxiolytic-like action of 24 h food deprivation in wild type mice was neutralized by administration of a GHSR antagonist further supported this conclusion (<xref ref-type="bibr" rid="B140">Lu et al., 2019</xref>).</p>
<p>In fear conditioning paradigms, caloric restriction and overnight fasting before extinction training were shown to enhance fear extinction and suppress return of fear in mice (<xref ref-type="bibr" rid="B187">Riddle et al., 2013</xref>; <xref ref-type="bibr" rid="B90">Huang et al., 2016</xref>; <xref ref-type="bibr" rid="B228">Verma et al., 2016</xref>), an effect that was abolished by administration of the GHSR antagonist D-Lys3 into the lateral amygdala (<xref ref-type="bibr" rid="B90">Huang et al., 2016</xref>). Interestingly, also in humans spontaneous recovery and reinstatement of fear were reduced after an overnight fast, which was correlated with ghrelin plasma levels (<xref ref-type="bibr" rid="B205">Shi et al., 2018</xref>). However, we could not confirm the extinction-promoting effect of overnight fasting using a weak extinction protocol and also found no difference between wild type and GHSR KO mice (<xref ref-type="bibr" rid="B179">Pierre et al., 2020</xref>). Thus, while manipulation of GHSR signaling may be an interesting avenue to curb fear expression or promote fear extinction, it appears that the experimental conditions under which such effects can be observed remain uncertain.</p>
</sec>
<sec id="S2.SS6">
<title>Summary, Shortcomings and Future Directions of Rodent Studies Investigating the Role of the Ghrelin System in Stress-Related Behaviors</title>
<p>The often mixed findings of rodent studies make it challenging to draw a general conclusion about the role of ghrelin and GHSR in stress-related behaviors. Possible reasons for these inconsistencies are diverse: the use of different mouse or rat strains, different age or sex of the animals, varying breeding, handling or habituation conditions, different time of day for testing and use of diverse behavioral and stress paradigms. The feeding status of the animals during testing may be of particular importance, as administration of exogenous ghrelin or GHSR agonists may confound the readout of behavioral assays by the instatement of hunger.</p>
<p>In summary, published literature suggests that the ghrelin system plays a different role in individuals depending on the amount and quality of previous stress exposure. This seems most obvious for GHSR signaling, which does not appear to affect fear, anxiety- and depression-like behaviors under non-stressed conditions but may exert mostly protective effects during chronic stress. A similar trend can be observed in pharmacological studies using GSHR ligands, where, without prior stress exposure, GHSR agonists predominantly promote anxiety- and depression-like behaviors, but seem to reduce chronic stress-related phenotypes. Also, caloric restriction may have beneficial effects on fear, anxiety- and depression-like behaviors in unstressed rodents through activation of GHSR. Nevertheless, the response of rodents to the potentially stressful nature of food deprivation might additionally challenge stress coping mechanisms and, together with differences in fasting procedures, contribute to inconsistencies in literature.</p>
<p>It has been proposed that prolonged elevation of plasma AG levels during chronic stress induces a central ghrelin resistance with reduced GHSR expression (<xref ref-type="bibr" rid="B80">Harmatz et al., 2016</xref>), which would impede ligand-dependent as well as ligand-independent GHSR signaling and thereby eliminate its protective role during stress. In the face of central ghrelin resistance, a rescue of stress-related phenotypes by AG or GHSR agonists as well as caloric restriction, which elevates endogenous ghrelin levels, seems unlikely. Nevertheless, many studies suggest beneficial effects of GHSR agonism and fasting on fear, anxiety-, and depression-like behaviors.</p>
<p>Only a few studies have considered the role of DAG in stress coping, although it constitutes the majority of total circulating plasma ghrelin and may have behavioral effects that are distinct from those of AG. This applies not only for feeding behaviors (<xref ref-type="bibr" rid="B57">Fernandez et al., 2016</xref>) but also for stress-related behaviors (<xref ref-type="bibr" rid="B218">Stark et al., 2016</xref>). This may be relevant during chronic stress and associated central ghrelin resistance, as AG can be rapidly converted to DAG (<xref ref-type="bibr" rid="B48">De Vriese et al., 2004</xref>), which appears to not act via the GHSR (<xref ref-type="bibr" rid="B20">Bednarek et al., 2000</xref>; <xref ref-type="bibr" rid="B58">Ferre et al., 2019</xref>). Thus, the reported beneficial effects of exogenous AG administration during chronic stress paradigms in rodents may be attributed to DAG rather than AG action. In this context, it also can be noted that the way of reporting plasma ghrelin levels has not been consistent in existing literature. Studies often report either only total or AG levels or do not specify acylation status at all, thereby hindering the overview of ghrelin alterations in baseline versus stressed conditions.</p>
<p>One more point to consider is that the GHSR may have functions independent from binding of AG, which is of particular importance since accessibility of many GHSR-expressing brain areas for the ghrelin peptide is not resolved yet (<xref ref-type="bibr" rid="B175">Perello et al., 2018</xref>). While the endogenous peptide LEAP2 has been shown to act as an antagonist/inverse agonist of the GHSR (<xref ref-type="bibr" rid="B61">Ge et al., 2018</xref>), it remains unknown to what extent it influences GHSR activity in different brain areas. Because of its high constitutive activity (<xref ref-type="bibr" rid="B87">Holst et al., 2003</xref>; <xref ref-type="bibr" rid="B177">Petersen et al., 2009</xref>) also changes in GHSR expression levels will accordingly alter activation of downstream signaling pathways as well as a possible formation of heterodimers with other receptors, such as receptors for dopamine and serotonin (<xref ref-type="bibr" rid="B201">Schellekens et al., 2013b</xref>; <xref ref-type="bibr" rid="B113">Kern et al., 2015</xref>). Given that heterodimer formation influences receptor signaling and trafficking (for review see <xref ref-type="bibr" rid="B199">Schellekens et al., 2013a</xref>; <xref ref-type="bibr" rid="B2">Abizaid and Hougland, 2020</xref>), this could serve to fine-tune GHSR signaling in response to certain neurotransmitters and, conversely, GHSR signaling would also affect these neurotransmitter systems. These complex (inter)actions of the GHSR could further result in individual differences, where an impairment of GHSR signaling occurs in stress-susceptible but not stress-resilient individuals, in which GHSR agonism still would have beneficial effects. Therefore, it might be useful to identify such individual differences in GHSR sensitivity and investigate which factors contribute to constitutive GHSR signaling.</p>
<p>Furthermore, this requires a clear distinction between findings from studies manipulating peptide hormone levels or using GHSR ligands (e.g., ghrelin KO mice, GOAT KO mice, pharmacological studies) versus studies conducted in GHSR KO mice. For a comprehensive dissection of the role of GHSR signaling in distinct neuronal populations, the development of new biomolecular tools like GHSR-Cre mice is indispensable in order to perform targeted pharmaco- and optogenetic manipulations and selectively employ new viral techniques. Such novel genetic and viral tools could also be used to create conditional knockouts of GHSR, GOAT or ghrelin. It cannot be excluded that in conventional germ-line knockouts compensatory mechanisms are at play that disguise the loss-of-function effect, thereby confounding results and leading to mixed findings and wrong conclusions.</p>
</sec>
</sec>
<sec id="S3">
<title>The Ghrelin System as a Novel Therapeutic Avenue in Stress-Related Psychiatric Disorders?</title>
<sec id="S3.SS1">
<title>A Need for New Treatment Strategies: Ghrelin as a Vantage Point?</title>
<p>In this review, we aimed to provide an overview of the current literature on the role of ghrelin system in stress coping. We summarized findings on fear, anxiety- and depression-like behaviors in rodent models and in this final chapter, we want to discuss the possible therapeutic utility of the ghrelin system in stress-related psychiatric disorders, with a focus on anxiety disorders and post-traumatic stress disorder (PTSD). They are the most common cause of psychiatric illness, with an estimated lifetime prevalence of up to 30% (<xref ref-type="bibr" rid="B115">Kessler et al., 2005a</xref>, <xref ref-type="bibr" rid="B117">2012</xref>) and women being affected almost twice as often as men (<xref ref-type="bibr" rid="B19">Baxter et al., 2013</xref>). Besides reducing the quality of life of patients and their families dramatically, they cause an immense socioeconomic burden in modern western societies (<xref ref-type="bibr" rid="B235">Wittchen et al., 2011</xref>; <xref ref-type="bibr" rid="B168">Olesen et al., 2012</xref>). However, a lack of major advances in psychopharmacotherapy over the past three decades as well as limited validity of current symptom-based diagnostic manuals (<xref ref-type="bibr" rid="B129">Lang et al., 2016</xref>) leave anxiety disorders and PTSD poorly diagnosed and undertreated (<xref ref-type="bibr" rid="B41">Craske et al., 2017</xref>). Moreover, a large number of anxiety patients do not show long-term benefit from currently available treatments and fail to achieve full remission or often relapse with time (<xref ref-type="bibr" rid="B86">Hofmann and Smits, 2008</xref>; <xref ref-type="bibr" rid="B16">Bandelow et al., 2015</xref>; <xref ref-type="bibr" rid="B119">Koek et al., 2016</xref>; <xref ref-type="bibr" rid="B41">Craske et al., 2017</xref>). Currently, there are also no biomarkers for the measurement of treatment response available (<xref ref-type="bibr" rid="B41">Craske et al., 2017</xref>). Thus, there is an urgent need for the development of novel strategies to augment existing diagnostic and treatment options to improve their efficiency and tackle under- and misdiagnosis as well as treatment resistance (<xref ref-type="bibr" rid="B210">Singewald et al., 2015</xref>; <xref ref-type="bibr" rid="B194">Sartori and Singewald, 2019</xref>).</p>
<p>There is a growing interest in the involvement and therapeutic potential of the ghrelin system in psychiatric diseases. Positioned at the interface between feeding circuitry, metabolism and the HPA axis, its dysregulation could not only potentially influence food intake and energy homeostasis but also stress vulnerability. This involvement of the ghrelin system in different physiological processes has sparked a discussion about its role in a variety of pathological conditions like obesity and eating disorders, but also addictive disorders as well as anxiety disorders, PTSD and mood disorders (for review see <xref ref-type="bibr" rid="B126">Labarthe et al., 2014</xref>; <xref ref-type="bibr" rid="B236">Wittekind and Kluge, 2015</xref>; <xref ref-type="bibr" rid="B15">Bali and Jaggi, 2016</xref>; <xref ref-type="bibr" rid="B221">Stievenard et al., 2016</xref>; <xref ref-type="bibr" rid="B104">Jiao et al., 2017</xref>; <xref ref-type="bibr" rid="B206">Shi et al., 2017</xref>). The potential role of the ghrelin system is further underscored by the notion that mood-, anxiety- and trauma-related disorders are often associated with metabolic dysregulation and also show a high level of comorbidity with obesity or eating disorders (<xref ref-type="bibr" rid="B203">Scott et al., 2008</xref>; <xref ref-type="bibr" rid="B164">Ng et al., 2013</xref>; <xref ref-type="bibr" rid="B145">Mason et al., 2014</xref>; <xref ref-type="bibr" rid="B152">Meng and D&#x2019;Arcy, 2015</xref>; <xref ref-type="bibr" rid="B1">Aaseth et al., 2019</xref>). It is very likely that comorbid diseases share a common neurobiological pathology, which could be of use to gain a better understanding of underlying disease mechanisms and to identify potential therapeutic targets.</p>
</sec>
<sec id="S3.SS2">
<title>(Dysregulation of) the Ghrelin System in Stress-Related Psychiatric Disorders</title>
<p>In humans, acute exposure to stressors is associated with elevated plasma ghrelin concentrations. In healthy individuals but also in obese patients with binge-eating disorder, total plasma ghrelin levels were elevated in those individuals who also had a high cortisol response to a Trier social stress test (TSST) (<xref ref-type="bibr" rid="B190">Rouach et al., 2007</xref>). Similarly, two studies with only female participants found elevated plasma cortisol and AG levels in healthy women (<xref ref-type="bibr" rid="B184">Raspopow et al., 2010</xref>) and higher saliva ghrelin but not cortisol levels in women suffering from bulimia nervosa (<xref ref-type="bibr" rid="B157">Monteleone et al., 2012</xref>) after stress exposure in a TSST. Other studies with only male participants reported no changes or, after alcohol consumption, even decreased AG levels following a TSST (<xref ref-type="bibr" rid="B247">Zimmermann et al., 2007</xref>) and no changes in total plasma ghrelin levels before and after a forced arithmetic task in a cohort of lean and obese men (<xref ref-type="bibr" rid="B128">Lambert et al., 2011</xref>). Taken together, these studies strongly suggest that the effects of acute stress exposure on plasma ghrelin levels may be dependent on sex. While the effects of chronic stress exposure have not been investigated explicitly in humans, one translational study reported elevated AG in teenagers 4.5 years after experiencing a severe traumatic event and proposed high plasma AG levels as a long-lasting biomarker for chronic stress exposure and a perpetuating risk factor for stress-enhanced fear (<xref ref-type="bibr" rid="B243">Yousufzai et al., 2018</xref>).</p>
<p>In line with the notion that alterations of the ghrelin system may be a biomarker for stress exposure, several other studies have investigated possible dysregulations of the ghrelin system in stress-related psychiatric disorders such as anxiety disorders, PTSD or major depressive disorder (MDD). The Gln90Le polymorphism in the pre-proghrelin gene has been linked to an increased risk of panic disorder (<xref ref-type="bibr" rid="B77">Hansson et al., 2013</xref>), while, in contrast, the Leu72Met variant of the pre-proghrelin gene was not associated with panic disorder (<xref ref-type="bibr" rid="B162">Nakashima et al., 2008</xref>) but with symptom severity in PTSD (<xref ref-type="bibr" rid="B135">Li et al., 2018</xref>) and MDD (<xref ref-type="bibr" rid="B162">Nakashima et al., 2008</xref>). A recent study reported elevated plasma ghrelin levels in children with a diagnosis of an anxiety disorder, which was more pronounced in girls than boys (<xref ref-type="bibr" rid="B169">Ozmen et al., 2019</xref>). Interestingly, ghrelin levels, serum cortisol and anxiety scores together with body mass index were more reduced in obese children following a combined dietary and mindfulness intervention in comparison to a control group that only underwent a dietary intervention (<xref ref-type="bibr" rid="B139">Lopez-Alarcon et al., 2020</xref>). However, in female patients diagnosed with anorexia nervosa or obesity, ghrelin levels were not correlated with depression- and anxiety-like symptoms independently of weight and body fat (<xref ref-type="bibr" rid="B130">Lawson et al., 2012</xref>). Numerous studies investigated plasma ghrelin levels in patients with MDD, which is often comorbid with anxiety- and trauma-related disorders and associated with stress-induced changes in food intake (<xref ref-type="bibr" rid="B114">Kessler, 1997</xref>, <xref ref-type="bibr" rid="B116">Kessler et al., 2005b</xref>; <xref ref-type="bibr" rid="B112">Kendler et al., 1999</xref>; <xref ref-type="bibr" rid="B66">Grant et al., 2013</xref>). They found increased fasting AG (<xref ref-type="bibr" rid="B125">Kurt et al., 2007</xref>; <xref ref-type="bibr" rid="B8">Algul and Ozcelik, 2018</xref>) and total ghrelin (<xref ref-type="bibr" rid="B170">Ozsoy et al., 2014</xref>), but also decreased fasting AG and DAG (<xref ref-type="bibr" rid="B18">Barim et al., 2009</xref>) or no changes in fasting AG or total ghrelin levels at all (<xref ref-type="bibr" rid="B197">Schanze et al., 2008</xref>; <xref ref-type="bibr" rid="B118">Kluge et al., 2010</xref>; <xref ref-type="bibr" rid="B63">Gimenez-Palop et al., 2012</xref>; <xref ref-type="bibr" rid="B147">Matsuo et al., 2012</xref>). Two of these studies showed a positive correlation of eating behavior with total ghrelin levels in MDD patients (<xref ref-type="bibr" rid="B197">Schanze et al., 2008</xref>; <xref ref-type="bibr" rid="B147">Matsuo et al., 2012</xref>), while another one reported lower AG levels in depressed patients with increased appetite (<xref ref-type="bibr" rid="B208">Simmons et al., 2020</xref>), indicating that plasma AG may not be good predictor for appetite or food intake in depressed patients.</p>
<p>The effect of treatment on ghrelin plasma levels in stress-related psychiatric disorders (mainly MDD) has also been examined. One study that found reduced plasma AG and DAG when comparing untreated MDD patients with healthy controls reported no effect of citalopram on ghrelin levels (<xref ref-type="bibr" rid="B18">Barim et al., 2009</xref>). Maprotiline treatment in male lean MDD patients, on the other hand, resulted in mildly increased plasma ghrelin levels (<xref ref-type="bibr" rid="B180">Pinar et al., 2008</xref>). In a mixed patient group suffering from bipolar disorder or MDD, serum AG levels were elevated compared to controls and decreased after electroconvulsive therapy (<xref ref-type="bibr" rid="B125">Kurt et al., 2007</xref>). A similar decrease in total ghrelin levels was reported in another study where patients received electroconvulsive therapy and/or different antidepressant drugs (<xref ref-type="bibr" rid="B170">Ozsoy et al., 2014</xref>). Interestingly, one study found, that therapy resistance in MDD and panic disorder was correlated with elevated AG (<xref ref-type="bibr" rid="B94">Ishitobi et al., 2012</xref>) and the effect of lithium augmentation treatment in treatment-resistant MDD could be characterized by a slight decrease in plasma AG in responders compared to an increase in non-responders (<xref ref-type="bibr" rid="B186">Ricken et al., 2017</xref>).</p>
<p>The conflicting findings in these studies probably result from confounding factors like nutritional status and time of day at sample collection, gender, age, body mass index, comorbid disorders and drug treatments, such as the type of antidepressant. Moreover, not all studies distinguished between AG and DAG and only measured total ghrelin levels or did not specify acylation status. Overall, it remains inconclusive whether genetic variants in the ghrelin system are causally involved in stress-related psychiatric disorders and whether altered ghrelin plasma levels are a predisposing factor for or just a byproduct of these diseases. Elevated plasma AG could indicate prior chronic stress exposure (<xref ref-type="bibr" rid="B243">Yousufzai et al., 2018</xref>), which in turn may enhance the risk for mental health disorders. Nevertheless, plasma AG appears to correlate with treatment resistance, suggesting more than mere association. Moreover, experiments in rodents indicate that stress-induced activation of the ghrelin system not only influences feeding but may also have a direct impact on fear, anxiety- and depression-like behaviors.</p>
</sec>
<sec id="S3.SS3">
<title>Therapeutic Potential of Targeting the Ghrelin System in Stress-Related Psychiatric Disorders</title>
<p>Despite the role of the ghrelin system in stress-related psychiatric disorders is not fully resolved yet, it provides a new and interesting vantage point in the search for more efficient diagnostic and therapeutic strategies (also see <xref ref-type="fig" rid="F1">Figure 1</xref>). It remains unknown whether a modulation of the ghrelin system could be beneficial in the treatment of stress-related psychiatric disorders, however multiple pharmacological tools to do so have become available over the last two decades (<xref ref-type="bibr" rid="B149">McGovern et al., 2016</xref>; <xref ref-type="bibr" rid="B132">Lee et al., 2020</xref>; <xref ref-type="bibr" rid="B158">Moose et al., 2020</xref>). This includes GHSR agonists and antagonists as well as inverse agonists and GOAT inhibitors, although no authorized medicine is commercially available to date. The pharmacological characterization of many ligands has only just begun and it will be of great importance to consider their central penetrance and possible signaling bias and further elucidate downstream signaling in order to allow targeted predictive modeling and the design of future ghrelin-based therapies (<xref ref-type="bibr" rid="B183">Ramirez et al., 2019</xref>; <xref ref-type="bibr" rid="B89">Howick et al., 2020</xref>). To our knowledge, there are currently no studies published that directly investigated the effect of ghrelin-targeted interventions in stress-related psychiatric conditions. One study in healthy human participants found enhanced extinction memory retention and reduced return of fear following an overnight fast, which was negatively correlated with ghrelin plasma levels (<xref ref-type="bibr" rid="B205">Shi et al., 2018</xref>). Whether fasting may improve exposure-based psychotherapy outcomes in patients with anxiety disorders or PTSD and whether this would be associated with changes in plasma AG concentrations or brain GHSR function remains to be established.</p>
<p>As a biomarker, high plasma AG could indicate prior stress exposure (<xref ref-type="bibr" rid="B243">Yousufzai et al., 2018</xref>), which in turn may enhance the risk for stress-related psychiatric disorders. While plasma AG concentrations were not consistently associated with disease, they may predict treatment resistance (<xref ref-type="bibr" rid="B94">Ishitobi et al., 2012</xref>; <xref ref-type="bibr" rid="B186">Ricken et al., 2017</xref>). In several studies, a decrease in plasma AG or total ghrelin levels during therapy was also associated with treatment response (<xref ref-type="bibr" rid="B125">Kurt et al., 2007</xref>; <xref ref-type="bibr" rid="B170">Ozsoy et al., 2014</xref>; <xref ref-type="bibr" rid="B186">Ricken et al., 2017</xref>; <xref ref-type="bibr" rid="B139">Lopez-Alarcon et al., 2020</xref>). A lack of changes in plasma AG concentrations may thus reflect decreased sensitivity of the GHSR and dysregulation of its feedback system. In light of our previous discussion that GHSR in the brain may act partly independent of circulating AG, this highlights the therapeutic potential for the development of diagnostic tools to study brain GHSR function in order to aid further stratification of patients for an optimization of treatment strategies.</p>
<p>It also should be kept in mind that potentially beneficial effects associated with activation of the ghrelin system, as observed in some rodent experiments, may be lost in patients with impaired GHSR function (<xref ref-type="bibr" rid="B80">Harmatz et al., 2016</xref>). To this end, a precise definition of the phenomenon of central ghrelin resistance and corresponding neurobiological correlates is indispensable. Present literature merely suggests an impaired feeding response following ghrelin (agonist) administration, associated with reduced c-Fos expression in the ARC (<xref ref-type="bibr" rid="B23">Briggs et al., 2010</xref>) and a reduction of AG binding (<xref ref-type="bibr" rid="B80">Harmatz et al., 2016</xref>) as markers for disrupted GHSR function. In addition, it is presently unclear whether fasting or other interventions could rapidly reverse central ghrelin resistance. A loss of GHSR function in hypothalamic NPY/AgRP neurons as a result of diet-induced obesity could be rescued by caloric restriction (<xref ref-type="bibr" rid="B23">Briggs et al., 2010</xref>, <xref ref-type="bibr" rid="B24">2013</xref>), but so far no study investigated whether this can be extrapolated to stress-induced central ghrelin resistance in brain regions beyond the hypothalamus. Instead of treatment, also a prevention of central ghrelin resistance could be considered. For example, a study in rats showed that administration of a GHSR antagonist during a chronic immobilization paradigm prevented the emergence of stress-enhanced fear (<xref ref-type="bibr" rid="B153">Meyer et al., 2014</xref>), while the same paradigm without GHSR antagonist administration led to reduced GHSR expression in the basolateral amygdala, which hampered the attenuation of stress-enhanced fear memories by a GHSR agonist (<xref ref-type="bibr" rid="B80">Harmatz et al., 2016</xref>). Therefore, preservation of GHSR function during chronic stress may keep the ghrelin system targetable for treatment interventions.</p>
<p>Also indirect targeting of the ghrelin system by other approaches may be of relevance in stress-related psychiatric disorders, for example via the gut microbiome (<xref ref-type="bibr" rid="B196">Schalla and Stengel, 2020</xref>). Changes in diet and gut microbiota composition have been linked to changes in plasma ghrelin levels in rodents and humans (for review see <xref ref-type="bibr" rid="B127">Lach et al., 2018</xref>). Moreover, it has been proposed that short-chain fatty acids produced by gastrointestinal microbiota may compete with octanoate for binding at the GOAT and interfere with the acylation of ghrelin (<xref ref-type="bibr" rid="B85">Heiman and Greenway, 2016</xref>). A recent study showed that different microbiota-derived metabolites, amongst them also short-chain fatty acids, may also directly attenuate GHSR signaling (<xref ref-type="bibr" rid="B226">Torres-Fuentes et al., 2019</xref>). Interestingly, one clinical study demonstrated that the use of dietary capsaicin altered gut microbiota composition and reduced ghrelin levels in healthy subjects (<xref ref-type="bibr" rid="B110">Kang et al., 2016</xref>). This is of particular interest, given that elevated plasma AG may reflect a higher risk for the development of stress-related psychiatric conditions (<xref ref-type="bibr" rid="B243">Yousufzai et al., 2018</xref>). Overall, this highlights the possibility of utilizing the gut microbiome to influence ghrelin signaling and thereby modulate the gut-brain axis in stress, although the underlying mechanisms how gut microbiota interact with the ghrelin system are not fully resolved yet.</p>
<p>We believe that the therapeutic potential of ghrelin-targeted interventions in stress-related psychiatric disorders is just starting to be explored. Especially a better understanding of the interactions of ghrelin with the HPA axis, the role of DAG versus AG and factors that control constitutive GHSR activity or lead to ghrelin resistance in the brain may uncover novel diagnostic and therapeutic avenues that have not been considered so far.</p>
</sec>
<sec id="S3.SS4">
<title>Interaction of Ghrelin With Neurotransmitter Systems as a Gateway to the Treatment of Psychiatric Disorders</title>
<p>Abundant evidence demonstrates interaction of the ghrelin system with different neurotransmitters, neuromodulators and their receptors, including monoamines, neuropeptides and endocannabinoids (<xref ref-type="bibr" rid="B26">Brunetti et al., 2002</xref>; <xref ref-type="bibr" rid="B214">Skibicka et al., 2012b</xref>; <xref ref-type="bibr" rid="B52">Edwards and Abizaid, 2016</xref>; <xref ref-type="bibr" rid="B84">Hedegaard and Holst, 2020</xref>). One possibility how the ghrelin system may affect behaviors relevant for psychiatric disorders is through its effect on the limbic system. These effects may result from direct activation of GHSR in different limbic areas like hippocampus or amygdala but may also be the consequence of activation of GHSR in neurotransmitter systems projecting to these limbic areas. In this regard, the effect of ghrelin signaling on the release of noradrenalin, serotonin and dopamine merits further discussion. Only few studies have investigated the effect of ghrelin on noradrenalin and serotonin release. One study found that peripheral ghrelin may activate the noradrenergic pathway from the hindbrain to the hypothalamus (<xref ref-type="bibr" rid="B46">Date et al., 2006</xref>) and another study reported that food deprivation and central administration of ghrelin augmented the increase of noradrenalin release in the PVN following foot shock stress in rats (<xref ref-type="bibr" rid="B111">Kawakami et al., 2008</xref>). Concerning ghrelin&#x2019;s effects on serotonin signaling, one study showed that ghrelin postsynaptically depolarized serotonin neurons in rat brain slices containing the dorsal raphe nucleus (<xref ref-type="bibr" rid="B166">Ogaya et al., 2011</xref>), while a second study found that ghrelin reduced the firing rate of dorsal raphe neurons in brain slices prepared from rats chronically treated with ghrelin (<xref ref-type="bibr" rid="B78">Hansson et al., 2011</xref>). Interestingly, acute central administration of ghrelin in mice was shown to increase serotonin turnover and the expression of serotonin-related genes in the amygdala (<xref ref-type="bibr" rid="B76">Hansson et al., 2014</xref>). While these studies demonstrate that ghrelin influences serotonin and noradrenaline signaling, the direct implications for fear, anxiety- and mood-related behaviors remain unclear.</p>
<p>Because the interaction of the ghrelin with the dopamine system is studied more extensively, we will further highlight certain aspects of this interaction and, as an example, discuss possible therapeutic relevance. Ghrelin was shown to modulate the spontaneous firing frequency of mesolimbic dopaminergic neurons in the VTA (<xref ref-type="bibr" rid="B3">Abizaid et al., 2006</xref>) and trigger dopamine release in the nucleus accumbens (NAc), predominantly in the shell region (<xref ref-type="bibr" rid="B100">Jerlhag et al., 2007</xref>; <xref ref-type="bibr" rid="B99">Jerlhag, 2008</xref>; <xref ref-type="bibr" rid="B181">Quarta et al., 2009</xref>; <xref ref-type="bibr" rid="B36">Cone et al., 2014</xref>). Associated with this rise of extracellular dopamine levels in the NAc following systemic or intra-VTA administration of ghrelin, stimulation of locomotor activity and conditioned place preference was observed (<xref ref-type="bibr" rid="B100">Jerlhag et al., 2007</xref>; <xref ref-type="bibr" rid="B99">Jerlhag, 2008</xref>). GHSR antagonism or a ghrelin KO, on the other hand, attenuated alcohol-, cocaine-, amphetamine- or morphine-induced locomotor stimulation and CPP and abolished the associated increase of accumbal dopamine release (<xref ref-type="bibr" rid="B101">Jerlhag et al., 2010</xref>; <xref ref-type="bibr" rid="B102">Jerlhag et al., 2011</xref>; <xref ref-type="bibr" rid="B55">Engel et al., 2015</xref>). In paradigms offering a free choice between standard chow and rewarding (palatable) food, ghrelin in the VTA stimulated hedonic feeding, but not homeostatic food intake (<xref ref-type="bibr" rid="B53">Egecioglu et al., 2010</xref>; <xref ref-type="bibr" rid="B212">Skibicka et al., 2011</xref>, <xref ref-type="bibr" rid="B215">2013</xref>; <xref ref-type="bibr" rid="B198">Schele et al., 2016</xref>). The mechanism via which ghrelin entrains the midbrain dopaminergic system, however, is not fully resolved yet. Recently, it was shown that ghrelin-binding cells are present in most subnuclei of the VTA, but not in the NAc (<xref ref-type="bibr" rid="B38">Cornejo et al., 2018</xref>). Moreover, Cornejo and colleagues demonstrated that centrally but not peripherally injected ghrelin recruits specific subsets of dopaminergic neurons in the parabrachial nucleus and GABAergic neurons in the interfascicular nucleus of the VTA (<xref ref-type="bibr" rid="B38">Cornejo et al., 2018</xref>). As for many other brain areas where the GHSR is expressed, there is no clear evidence whether peripherally circulating ghrelin reaches the VTA and directly acts on midbrain dopaminergic neurons (<xref ref-type="bibr" rid="B175">Perello et al., 2018</xref>). Also indirect mechanisms of activation (e.g., via orexigenic neurons in the lateral hypothalamus) have yet to be elucidated (<xref ref-type="bibr" rid="B182">Quarta and Smolders, 2014</xref>; <xref ref-type="bibr" rid="B6">Al Massadi et al., 2019</xref>). Furthermore, it has been proposed that (hippocampal) dopamine signaling is dependent on heterodimerization between dopamine D1 (DRD1) and GHS receptors, regulating DRD1-induced hippocampal synaptic plasticity and learning (<xref ref-type="bibr" rid="B113">Kern et al., 2015</xref>).</p>
<p>The role of ghrelin signaling on mesolimbic dopamine was previously reviewed extensively in the context of food reward (<xref ref-type="bibr" rid="B211">Skibicka and Dickson, 2011</xref>; <xref ref-type="bibr" rid="B176">Perello and Zigman, 2012</xref>; <xref ref-type="bibr" rid="B213">Skibicka et al., 2012a</xref>; <xref ref-type="bibr" rid="B137">Liu and Borgland, 2015</xref>; <xref ref-type="bibr" rid="B6">Al Massadi et al., 2019</xref>). However, these actions of ghrelin may also be relevant for stress-related psychiatric disorders. A possible role in mood disorders seems likely, given that ghrelin has been proposed to mediate CSDS-induced food reward (<xref ref-type="bibr" rid="B35">Chuang et al., 2011</xref>) and protect against depressive-like symptoms following CSDS in mice (<xref ref-type="bibr" rid="B142">Lutter et al., 2008</xref>). This is further corroborated by the observation that hyperphagic depressed patients showed a greater change in AG in response to a meal, which was associated with increased activity in the VTA (<xref ref-type="bibr" rid="B34">Cerit et al., 2019</xref>). As such, ghrelin signaling on mesolimbic dopamine neurons may indeed constitute the interface of stress, mood and food reward (<xref ref-type="bibr" rid="B200">Schellekens et al., 2012</xref>). With respect to anxiety disorders and PTSD, the abundant expression of the GHSR and GHSR mRNA on/in midbrain dopamine neurons of the VTA (<xref ref-type="bibr" rid="B246">Zigman et al., 2006</xref>; <xref ref-type="bibr" rid="B144">Mani et al., 2014</xref>) is particularly interesting (<xref ref-type="fig" rid="F1">Figure 1</xref>), as accumulating evidence suggests midbrain dopaminergic signaling as an important player in fear extinction (<xref ref-type="bibr" rid="B4">Abraham et al., 2014</xref>; <xref ref-type="bibr" rid="B107">Kalisch et al., 2019</xref>). The extinction of fear is the driving mechanism behind the reduction of fear responses and very basis of exposure-based cognitive behavioral therapy (<xref ref-type="bibr" rid="B154">Milad and Quirk, 2012</xref>), which is first-line in the treatment of anxiety- and trauma-related disorders (<xref ref-type="bibr" rid="B40">Craske, 2010</xref>; <xref ref-type="bibr" rid="B41">Craske et al., 2017</xref>). Also translationally, this paradigm is very appealing as it is easy to model in the laboratory in rodent models as well as humans (<xref ref-type="bibr" rid="B154">Milad and Quirk, 2012</xref>; <xref ref-type="bibr" rid="B209">Singewald and Holmes, 2019</xref>). Moreover, impaired fear extinction was suggested as a relevant endophenotype for anxiety disorders and PTSD (<xref ref-type="bibr" rid="B209">Singewald and Holmes, 2019</xref>). Recently, it has been proposed that during extinction learning midbrain dopaminergic neurons encode a quasi-appetitive reward prediction error, signaling the omission of the aversive unconditioned stimulus as a &#x2018;better-than-expected&#x2019; outcome (<xref ref-type="bibr" rid="B141">Luo et al., 2018</xref>; <xref ref-type="bibr" rid="B193">Salinas-Hernandez et al., 2018</xref>; <xref ref-type="bibr" rid="B29">Cai et al., 2020</xref>). Besides this temporally restricted role in extinction acquisition, dopamine was also suggested to play a key role in the consolidation phase in a human fMRI study (<xref ref-type="bibr" rid="B62">Gerlicher et al., 2018</xref>). In a collaborative study, our lab has previously shown that enhancing dopaminergic signaling by L-DOPA treatment helps the formation of long-lasting extinction memories and prevents return of fear in extinction-competent mice and healthy humans (<xref ref-type="bibr" rid="B74">Haaker et al., 2013</xref>). Moreover, we were able to show that L-DOPA treatment can rescue deficient fear extinction in a mouse model for refractory anxiety disorders (<xref ref-type="bibr" rid="B233">Whittle et al., 2016</xref>).</p>
<p>Despite this clear evidence of interaction of the two systems, very few studies have investigated the possible benefits of targeting the ghrelin-dopamine axis in stress-related psychiatric disorders. We were able to show recently, that administration of the ghrelin agonist MK0677 directly into the VTA induces dopamine release in the NAc but also in amygdala and medial prefrontal cortex, which are important parts of fear and anxiety circuitries (<xref ref-type="bibr" rid="B179">Pierre et al., 2020</xref>). But despite increasing dopamine release in VTA projection areas, in our hands, MK0677 did not influence fear acquisition or extinction and extinction memory retrieval in unstressed mice. One explanation could be that the achieved rise in dopamine may not have been sufficient or not timed adequately, which may be enhanced by optimizing ghrelin agonists, dosage and ways of administration. Since the elucidation of the exact role of dopamine during fear extinction has only begun, advances in this field could help to utilize the ghrelin-dopamine axis in a more targeted manner (e.g., timing, individual differences) in future studies.</p>
</sec>
</sec>
<sec id="S4">
<title>Conclusion and Future Directions</title>
<p>Although the body of literature about the ghrelin system is growing rapidly, a great amount of questions regarding its effect on brain function remain unanswered. This complicates the evaluation of pathological relevance and therapeutic utility of ghrelin and GHSR in stress-related psychiatric disorders. To this end, a better understanding of the role of the ghrelin system in stress coping and its interplay with the HPA axis will be important. Further studies will be necessary to characterize brain GHSR signaling beyond the action of AG on its receptor, as DAG and ligand-independent GHSR activity have received little attention in existing literature. Moreover, the phenomenon of central ghrelin resistance in chronic stress needs to be studied more intensely in order to establish associated neurobiological correlates. The notion that ghrelin modulates fear, anxiety- and depression-like behaviors as a stress hormone seems to arise mostly from rodent experiments, while evidence from human studies is sparse and inconclusive. Nevertheless, it appears evident that ghrelin is much more than a &#x2018;hunger hormone&#x2019; and represents an interesting target for novel interventions in stress-related psychiatric disorders that will become more accessible once its dynamics in the context of stress are better understood.</p>
</sec>
<sec id="S5">
<title>Author Contributions</title>
<p>EMF and DDB conceptualized the review and performed literature research. EMF wrote the manuscript with contributions and supervision from DDB. DDB and NS reviewed and revised all sections. All authors read and approved the final manuscript.</p>
</sec>
<sec id="conf1">
<title>Conflict of Interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
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<back>
<fn-group>
<fn fn-type="financial-disclosure">
<p><bold>Funding.</bold> This work was supported by the Austrian Science Fund (FWF, I2433-B26 and DKW-1206-B18) and the Fund for Scientific Research Flanders (FWO-G001816N and FWO-11ZL616N) and the Strategic Research Programme of the Vrije Universiteit Brussel (SRP49).</p>
</fn>
</fn-group>
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<title>Abbreviations</title>
<def-list id="DL1">
<def-item><term>ACTH</term><def><p>adrenocorticotropic hormone</p></def></def-item>
<def-item><term>AG</term><def><p>acyl ghrelin</p></def></def-item>
<def-item><term>AGRP</term><def><p>agouti-related peptide</p></def></def-item>
<def-item><term>ARC</term><def><p>arcuate nucleus</p></def></def-item>
<def-item><term>CPP</term><def><p>conditioned place preference</p></def></def-item>
<def-item><term>CRF</term><def><p>corticotropin-releasing factor</p></def></def-item>
<def-item><term>CSDS</term><def><p>chronic social defeat stress</p></def></def-item>
<def-item><term>CUMS</term><def><p>chronic mild unpredictable stress</p></def></def-item>
<def-item><term>DAG</term><def><p>desacyl ghrelin</p></def></def-item>
<def-item><term>GABA</term><def><p>gamma aminobutyric acid</p></def></def-item>
<def-item><term>GHSR</term><def><p>ghrelin receptor (growth hormone secretagogue receptor)</p></def></def-item>
<def-item><term>GOAT</term><def><p>ghrelin-O-acyltransferase</p></def></def-item>
<def-item><term>HFD</term><def><p>high-fat diet</p></def></def-item>
<def-item><term>HPA</term><def><p>hypothalamic-pituitary-adrenal</p></def></def-item>
<def-item><term>KO</term><def><p>knockout</p></def></def-item>
<def-item><term>LEAP2</term><def><p>liver-expressed antimicrobial peptide 2</p></def></def-item>
<def-item><term>LPS</term><def><p>lipopolysaccharide</p></def></def-item>
<def-item><term>MDD</term><def><p>major depressive disorder</p></def></def-item>
<def-item><term>NAc</term><def><p>nucleus accumbens</p></def></def-item>
<def-item><term>NG</term><def><p>nodose ganglion</p></def></def-item>
<def-item><term>NPY</term><def><p>neuropeptide Y</p></def></def-item>
<def-item><term>NTS</term><def><p>nucleus tractus solitarius</p></def></def-item>
<def-item><term>PTSD</term><def><p>post-traumatic stress disorder</p></def></def-item>
<def-item><term>PVN</term><def><p>paraventricular nucleus</p></def></def-item>
<def-item><term>TSST</term><def><p>Trier social stress test</p></def></def-item>
<def-item><term>VTA</term><def><p>ventral tegmental area.</p></def></def-item>
</def-list>
</glossary>
</back>
</article>