The hop constituent xanthohumol exhibits hepatoprotective effects and inhibits the activation of hepatic stellate cells at different levels
- 1Institute of Molecular Pathobiochemistry, Experimental Gene Therapy and Clinical Chemistry, RWTH University Hospital Aachen, Aachen, Germany
- 2Department of Internal Medicine I, University Hospital Regensburg, Regensburg, Germany
Xanthohumol is the principal prenylated flavonoid of the female inflorescences of the hop plant. In recent years, various beneficial xanthohumol effects including anti-inflammatory, antioxidant, hypoglycemic activities, and anticancer effects have been revealed. This review summarizes present studies indicating that xanthohumol also inhibits several critical pathophysiological steps during the development and course of chronic liver disease, including the activation and pro-fibrogenic genotype of hepatic stellate cells. Also the various mechanism of action and molecular targets of the beneficial xanthohumol effects will be described. Furthermore, the potential use of xanthohumol or a xanthohumol-enriched hop extract as therapeutic agent to combat the progression of chronic liver disease will be discussed. It is notable that in addition to its hepatoprotective effects, xanthohumol also holds promise as a therapeutic agent for treating obesity, dysregulation of glucose metabolism and other components of the metabolic syndrome including hepatic steatosis. Thus, therapeutic xanthohumol application appears as a promising strategy, particularly in obese patients, to inhibit the development as well as the progression of non-alcoholic fatty liver disease.
Hop (Humulus lupulus L.) has been used since ancient times as a medicinal plant. Traditional medicinal indications included the treatment of anxiety and insomnia, mild pain reduction or combating dyspepsia (Zanoli and Zavatti, 2008). Today, hops are used in the manufacturing of beer and female infertile plants are cultivated on high trolleys especially for brewing (Figure 1A). Biologically active substances, which are also important for brewing, are concentrated inside hop cones (Figure 1B) in lupulin glands (Figure 1C) which contain hop resins, bitter acids, essential oils and prenylated flavonoids. These lupulin glands are tiny yellow sacs that are located at the base of the petals of the hop cone (Figure 1D) that are found in female plants, while cones from the male hop plant contain relatively few lupulin glands.
Figure 1. Hop plant and xanthohumol. (A) Hop plant (Humulus lupulus) field in Bavaria, showing the typical form of cultivation on high trolleys. (B) Female hop flowers (hop cones), where the biologically active substances, which are also important for brewing, are concentrated inside in the lupulin glands; (C) lupulin glands, which contain hop resins, bitter acids, essential oils and prenylated flavonoids. (D) Schematic drawing of a female hop cone that is composed of a central spine (i.e., the strig), bracts (i.e., pear-shaped petal that does not contain lupulin glands), bracteoles (i.e., pear-shaped petal of the hop cone that shelters the lupulin glands and any seeds that may be present), and the characteristic lupulin glands that are tiny yellow sacs containing the hop oils. (E) Chemical structure of xanthohumol (3′-[3,3-dimethyl allyl]-2′,4′,4-trihydroxy-6′-methoxychalcone), the major prenylated chalcone of the hop plant.
Xanthohumol (XN; 3′-[3,3-dimethyl allyl]-2′,4′,4-trihydroxy-6′-methoxychalcone) is the principal prenylated chalcone of the hop plant (Figure 1E). The yellow compound (Greek: xantho = yellow) is found in high quantities in the lupulin glands. Since the 1990s, interest in health-promoting activities of XN increased constantly, scientific investigations were initialized worldwide and papers and patents on this topic have increased steadily (Gerhauser and Frank, 2005).
Many studies identified XN as a broad-spectrum cancer chemopreventive agent acting by multiple mechanisms relevant for cancer development and progression (Gerhauser et al., 2002). XN is able to scavenge reactive oxygen species and it modulates many enzymes involved in carcinogen metabolism and detoxification (Gerhauser et al., 2002). Furthermore, XN inhibits cyclooxygenase 2 (COX-2) expression and the activity of both Cox-1 and Cox-2 in lipopolysaccharide-mediated iNOS induction in the macrophages (Stevens and Page, 2004). XN also has been shown to decrease prostaglandin-E2 (PGE2) expression (Jongthawin et al., 2012). These anti-inflammatory properties may contribute to the inhibition of tumor promotion by the inhibition of nuclear factor-κB (NF-κB) signaling and subsequent down-regulation of pro-inflammatory factors (Albini et al., 2006; Colgate et al., 2007). Moreover, estrogen-mediated tumor promotion may be prevented by XN, which suppresses estrogen-signaling through the inhibition of the interaction between the oncoprotein brefeldin A-inhibited guanine nucleotide-exchange protein 3 (BIG3) and tumor suppressor prohibitin 2 (PHB2) (Yoshimaru et al., 2014). XN also inhibits the enzyme aromatase (CYP19), which plays a crucial role in the conversion of testosterone to estrogen (Monteiro et al., 2006). Furthermore, XN inhibits tumor cell growth by different mechanism such as decrease of DNA polymerase alpha activity and inhibition of DNA synthesis (Gerhauser et al., 2002). Moreover, XN induces apoptosis by poly(ADP-ribose)polymerase (PARP) cleavage, activation of caspases or down-regulation of Bcl-2 protein expression (Pan et al., 2005). XN has further been shown to modulate drug metabolism in vitro by inhibition of various Cyp enzymes and by induction of quinone reductase activity (Henderson et al., 2000; Miranda et al., 2000a), which has been considered as a biomarker for cancer chemoprevention (Cuendet et al., 2006). In addition to the molecular mechanism by which XN affects cancer cells, it has been shown to exhibit several further biological effects (Figure 2) which are also playing an important role during the course of chronic liver disease. Hepatic fibrosis is the peril that determines morbidity and mortality in patients with liver disease. Cirrhosis, as the end stage of hepatic fibrosis, is a major clinical issue for its high prevalence in the world and its tight relationship with hepatocellular carcinoma (HCC) incidence (Gines et al., 2004; Villanueva et al., 2007; Minguez et al., 2009). The activation of hepatic stellate cells (HSC) is the key event of hepatic fibrosis (Lang and Brenner, 1999; Kisseleva and Brenner, 2007; Elpek, 2014). Activated HSC/myofibroblasts are the cellular source of the excessive extracellular matrix (ECM) deposition (Lang and Brenner, 1999; Kisseleva and Brenner, 2007). Furthermore, activated HSC/myofibroblasts form and infiltrate the tumor stroma and promote HCC progression (Amann et al., 2009). Therefore, these cells are a critical target for therapy during the whole course of chronic liver disease. However, up to date, no effective therapy is available to block the activation of HSC or to inhibit the pro-inflammatory and pro-fibrogenic activity of the activated HSC. In the following, we provide a summary of present studies indicating the potential of this hop constituent as a therapeutic agent to beneficially affect hepatic fibrosis as well as various further pathological mechanisms during the course of chronic liver disease.
Figure 2. Biological effects of xanthohumol. Xanthohumol (XN) has been shown to have wide spectrum of biological effects, by which it may also affect different pathophysiological mechanisms involved in the development and progression of chronic liver disease. Studies have shown that XN acts anti-angiogenic (Albini et al., 2006; Shamoto et al., 2013), anti-carcinogenic (Dorn et al., 2010a,b,c; Araujo et al., 2011), chemopreventive (Miranda et al., 2000c; Gerhauser et al., 2002; Dorn et al., 2010a), anti-microbial (Gerhauser and Frank, 2005; Rozalski et al., 2013; Kramer et al., 2015), anti-viral (Buckwold et al., 2004; Zhang et al., 2009, 2010; Lou et al., 2014), anti-inflammatoric (Dorn et al., 2010a, 2013; Jongthawin et al., 2012), as a ROS scavenger (Gerhauser et al., 2002), anti-diabetic (Legette et al., 2013), and anti-oxidative (Gerhauser et al., 2002). In regard to liver fibrogenesis, it was shown that XN has anti-fibrogenic potential (Dorn et al., 2010a, 2013; Yang et al., 2013) and inhibits HSC activation and proliferation (Dorn et al., 2010a). Moreover, XN improves the metabolic syndrome (Legette et al., 2013).
Effects of Xanthohumol on Hepatic Stellate Cells in vitro
As already mentioned, the activation of HSC plays a critical pathophysiological role in the progression of chronic liver disease and the activation of these cells in response to liver injury is considered as the key event of hepatic fibrosis (Bataller and Brenner, 2001). Interestingly, XN has been shown to inhibit the activation of primary human HSC in vitro in concentrations as low as 5 μM XN (Dorn et al., 2010a). Furthermore, XN induced apoptosis in activated HSC in vitro in a dose-dependent manner (0–20 μM). Moreover, XN reduced expression of the pro-inflammatory factors such as the monocyte chemoattractant protein-1 (MCP-1) or pro-fibrogenic genes such as type I collagen in HSC. MCP-1 is regulated by NF-κB and increased levels are associated with fibrosis progression in chronic liver disease (Jarrar et al., 2008; Wouters et al., 2008). Further, NF-κB activation is a central pathophysiological mechanism during HSC activation (Hellerbrand et al., 1998a,b; Elsharkawy et al., 2005). Importantly, XN inhibited NF-κB activity in activated HSC in vitro (Dorn et al., 2010a). In summary, in vitro studies revealed that XN inhibits several key pathological factors of HSC activation and their contribution to fibrosis progression in chronic liver disease (Figure 3). In addition, XN has been shown to inhibit HSC-activation and hepatic fibrosis in experimental models of liver injury (please see below). Future research, may aim at the identification of further molecular pathways which may contribute to the anti-fibrogenic effect of XN in HSC.
Figure 3. Reported in vitro effects of xanthohumol in hepatic stellate cells. Xanthohumol (XN) inhibits the activation of hepatic stellate cells (HSC) as well as several key pathological factors of activated HSC including pro-inflammatory and -fibrogenic gene expression, proliferation, apoptosis resistance, and composition of extracellular matrix. In particular, it is known that XN inhibits pro-inflammatory and pro-fibrogenic (Dorn et al., 2010a, 2013) gene expression and HSC activation (Yang et al., 2013) thereby preventing the excessive formation and deposition of extracellular matrix as well as the activation and proliferation of HSC. In addition, XN was shown to interfere with HSC apoptosis (Dorn et al., 2010a).
Anti-viral and Antimicrobial Activities of XN
HSC activation occurs in response to hepatocellular injury, and hepatitis C virus (HCV) infection is a one of the major causes of liver infectious diseases. In vitro studies using virus that causes bovine diarrhea (bovine viral diarrhea virus - BVDV E2), which shows considerable similarities with the human HCV, showed that XN inhibits BVDV replication and enhanced the anti-viral activity of interferon (IFN)-α (Buckwold et al., 2004; Zhang et al., 2009, 2010). Antiviral activity of XN in combination with IFNα-2b, was also demonstrated against herpes simplex virus and cytomegalovirus (Buckwold et al., 2004). More recently, XN was examined for its ability to inhibit HCV virus replication in a cell culture system carrying replicating HCV RNA replicon and it was shown that XN has similar inhibitory effects as IFNα-2b (Lou et al., 2014). Bacteria and bacterial translocation from the intestine have been shown to promote the progression of chronic liver disease, including HSC-activation and fibrogenesis (Seki et al., 2007). More recently, it has been shown that antibiotics improved the intestinal permeability and attenuated liver fibrosis development associated with Nonalcoholic Steatohepatitis (NASH) via the inhibition of HSC activation (Douhara et al., 2015). With regards to this, it is important, that the broad spectrum of antimicrobial activity of XN is well known (Gerhauser, 2005). More recently, the inhibitory effect of a hop extract containing XN was demonstrated against different gram-positive bacteria including Listeria monocytogenes and Staphylococcus aureus (Kramer et al., 2015).
In summary, there is a high rationale that XN may exhibit beneficial effects in liver disease also via inhibiting bacterial translocation or the growth of (gram-positive) bacteria. Still experimental proof of this hypothesis is missing, which may be the subject of future research in appropriate (in vivo) models or clinical studies.
XN Effects on Hepatocellular Cancer Cells and Primary Hepatocytes
As already mentioned, a number of studies indicated the potential of XN to prevent and treat different types of cancers (Araujo et al., 2011). In the pathogenesis of HCC, XN exhibited anti-tumorous effects and induced the apoptosis in two different human HCC cell lines (HepG2 and Huh7) in vitro at concentration of 25 μM (Dorn et al., 2010b). Furthermore, XN repressed proliferation and migration in both cell lines even at lower concentrations (Dorn et al., 2010a). In a study with HepG2 cells, anti-mutagenic effects of XN were demonstrated even at concentrations of 0.01–0.1 μM (Plazar et al., 2008; Viegas et al., 2012). Chemopreventative effects can also occur by detoxifying carcinogens through the action of specific enzymes. One of these enzymes is NAD(P)H: quinone reductase that catalyzes the reduction of quinone to hydroquinones, which are more suitable substrates for subsequent conjugation. It was found that XN increased by several fold the activity of quinone reductase in murine liver cells (Hepa-1c1c7) (Miranda et al., 2000b) at concentrations above 1 μM. Importantly, even at XN concentrations as high as 100 μM, XN did not affect the viability of primary human hepatocytes in vitro (Dorn et al., 2010a).
It should be noted that in cellular experiments performed with XN the reproducibility of all these findings might be affected by the low solubility of XN in cell culture medium, the composition of media used, the tendency of XN to absorb to various plastic materials routinely used in the cell culture, and the reduction of the effective XN dose by conversion to isoxanthohumol (Motyl et al., 2012). Likewise, the bioavailability of XN and its prenylated flavanone (i.e., Isoxanthohumol) is marked by inter-individual variability that is induced by variations in the intestinal microbial community and their degradation pathways that have direct impact on biotransformation of respective compounds (Possemiers et al., 2005).
Therefore, studies that investigate pharmacological effects of XN or its natural or synthetic derivatives should punctiliously describe all details of the chosen experimental setting, not only including sources and concentrations of employed prenylflavonoid but also specification of media and buffer composition, identity and origin of cell lines and animals, details about culture conditions, animal accommodation, supplier of plastic ware, and many others.
Furthermore, future research may focus on the identification of (downstream) signaling pathways responsible for xanthohumol effects in hepatocytes. Recently, it has been shown that the activation of Nrf2 pathway and subsequently phase II enzymes in concert with p53 induction may account for the molecular mechanism of the chemopreventive activity of XN in hepatocytes (Krajka-Kuzniak et al., 2013). On the other hand its cytotoxicity toward HCC cells indicates that it may also be considered as potentially chemotherapeutic (Dorn et al., 2010a). Moreover, the antimutagenic effects of XN were demonstrated against various procarcinogens, which are activated by cytochrome P450 enzymes (Plazar et al., 2007; Ferk et al., 2010). The mechanisms are possibly related to the inhibition of the metabolic activation by human cytochrome P450 1A2 (CYP1A2) and inhibition of the binding of the metabolites to DNA and proteins (Miranda et al., 2000c). Moreover, XN interferes with several stages in the angiogenic process, including inhibition of endothelial cell invasion and migration, growth, and formation of tubular-like structures (Gerhauser et al., 2002; Albini et al., 2006). The mechanisms for its inhibition of angiogenesis are related to the blockage of both the nuclear factor-κB (NFκB) and Akt pathways in endothelial cells (Albini et al., 2006). Furthermore, in addition to the direct effect of XN on the vascular cells, XN inhibits the production of angiogenic factors, e.g., vascular endothelial growth factor (VEGF) and interleukin 8 (IL-8) via the inhibition of NF-κB (Shamoto et al., 2013). Still, according analyses in primary hepatocytes are missing.
XN Effects in Models of Acute Liver Injury
There is already a multitude of reports describing beneficial effects of XN on liver injury in vitro and in vivo (Table 1). Hepatic ischemia/reperfusion (I/R) injury occurs in a variety of clinical scenarios, including transplantation, liver resection, trauma, and hypovolemic shock. The process of hepatic I/R-injury can be divided into two phases; an acute phase (the first 6 h after reperfusion) and the following sub-acute phase (Fan et al., 1999). The acute phase is characterized by generation of reactive oxygen species (ROS) subsequent to reoxygenation of the liver leading to marked hepatocellular damage (Parks and Granger, 1988; Rauen et al., 1994). Noteworthy, pretreatment of mice with XN (1,000 mg/kg body weight for 5 days) significantly ameliorated I/R-induced oxidative stress 6 h after reperfusion (Dorn et al., 2013). Although hepatocellular damage was not modulated at this early phase, the I/R-induced NF-κB activation and pro-inflammatory gene expression was almost completely blunted (Dorn et al., 2013). These factors play a crucial role in the later course of hepatic I/R-injury via recruitment and activation of pro-inflammatory cells (Jaeschke et al., 1992; Jaeschke, 1996). Also in an ex vivo-model of cold hepatic I/R XN revealed an antioxidant and inhibitory effect on NF-κB activity (Hartkorn et al., 2009).
The liver is also frequently exposed to various insults, including toxic chemicals (Zimmerman and Lewis, 1995; Grunhage et al., 2003). Liver damage caused by hepatotoxic chemicals induces liver necrosis due to direct damage of hepatocytes and subsequent inflammation (Mehendale et al., 1994). Carbon tetrachloride (CCl4), an industrial solvent, is a hepatotoxic agent and its administration is widely used as an animal model of toxin-induced liver injury that allows the evaluation of both necrosis and subsequent inflammation (Huh et al., 2004) as well as fibrosis (Iredale, 2007). In this model, oral application of XN (500 mg/kg BW) was shown to significantly inhibit the pro-inflammatory and pro-fibrogenic hepatic gene expression (Dorn et al., 2012). Noteworthy, these effects occurred despite the fact that hepatocellular injury as reflected by serum levels of transaminases or histomorphological analysis was comparable between control mice and XN-fed mice. These findings suggest that the suppressive effect of XN against the progress of acute CCl4-induced hepatic fibrosis involved direct mechanisms related to its ability to block both hepatic inflammation and the activation of HSC.
In summary, these findings indicate the potential of XN to exhibit a beneficial effect in acute liver injury or failure. Still, it has to be mentioned that in the studies cited above XN has be applied before the onset of liver injury, i.e., prevented acute liver injury in experimental models. Further studies are warranted to analyzed the therapeutic potential of XN, i.e., after the onset of liver injury. A further potential clinical application of XN might be the prevention of oxidative stress in conservation solutions during the organ transplantation process. However, also here, future studies are warranted.
Effect of XN in Models of Chronic Liver Injury
Chronic HCV infection is one of the most frequent liver diseases worldwide (Yang et al., 2013). In an elegant study, Yang et al. analyzed the hepatoprotective effect of XN in an in vivo model of HCV infected Tupaias. XN was applied by gavage at a dose of 100 mg/kg BW which led to a significant reduction of hepatic inflammation and fibrosis compared to control animals. Interestingly, XN also inhibited the hepatic steatosis in this model, which was found to be related to an inhibitory effect on microsomal triglyceride transfer protein activity and inhibition of hematopoietic stem cells (Yang et al., 2013).
Besides alcohol abuse, non-alcoholic fatty liver disease (NAFLD) has emerged as the most frequent liver disease in Western countries (Clark et al., 2002; Cobbold et al., 2010; Vernon et al., 2011). Today, the metabolic syndrome (MS) is one of the major public health challenges worldwide that is characterized by clustering of waist circumference, blood triglycerides, high density lipoprotein (HDL) cholesterol and fasting glucose levels. MS is also closely associated with NAFLD, and thus today, NAFLD is considered as a component of the MS (reviewed in Saidijam et al., 2014). MS affects approximately 25 per cent of the adult population in Western countries and also is quickly increasing in young populations. Accordingly, also NAFLD incidence is further increasing and effective strategies to prevent the development and progression of NAFLD to its advanced form NASH are urgently needed. Of note, XN has been shown to exhibit a beneficial effect in different experimental NAFLD models. Yui et al. reported that feeding rats a high-fat diet enriched with XN extract (1% w/w equivalent to a dose of 100 mg/kg BW) inhibited the increase of body and liver weight, as well as triacylglycerol levels in the plasma and in the liver (Yui et al., 2014). The mechanisms were found to be related to the regulation of the hepatic fatty acid metabolism and an inhibition of fat absorption in the intestine (Doddapattar et al., 2013). In this study, XN also tended to reduce hepatic fatty acid synthesis through the reduction of hepatic sterol regulatory element-binding protein (SREBP) 1c mRNA expression in rats fed with a high-fat diet. Furthermore, it was observed that plasma adiponectin levels tended to be elevated by dietary application of the XN-rich hop extract (Yui et al., 2014). Also in a second model, in which NASH was induced by feeding the mice with an NASH-inducing diet, XN exhibited anti-inflammatory and anti-fibrogenic effects (Dorn et al., 2010a). Here, XN was applied in the diet in a concentration of 1% W/W corresponding to a dose of approximately 1000 mg/kg BW. In this model, after 3 weeks feeding, the induction of hepatic inflammation and pro-fibrogenic gene expression was almost completely blunted in mice receiving XN-supplemented NASH diet compared to mice fed with the pure NASH-diet (Dorn et al., 2010a).
Moreover, ApoE−/− mice showed decreased hepatic triglyceride and cholesterol content, activation of AMP-activated protein kinase, phosphorylation and inactivation of acetyl-CoA carboxylase, and reduced expression levels of mature SREBP-1c upon 8 weeks XN feeding (300 mg/kg BW/day) (Doddapattar et al., 2013).
In summary, XN has been shown to beneficially affect several components of the metabolic syndrome. Furthermore, it positively affects other obesity associated pathological factors such as misbalance of adipokine levels, which are known to promote NAFLD development and progression. Fitting to this is the beneficial effect of XN on hepatic steatosis, inflammation and fibrosis in experimental NASH models. In addition to NAFLD/NASH, XN revealed positive effects in other experimental models of chronic liver injury such as HCV, which can be explained by the above described inhibitory effects on fibrogenic and inflammatory gene expression or anti-bacterial effects. Still, it has to be noted that in the published studies, XN was applied in a preventive experimental setting. Future studies are warranted to analyze the potential of XN to treat, i.e., stop or reverse liver fibrosis.
Pharmacokinetics and Effective Dose of XN
Recent studies enhanced our knowledge regarding metabolisms and pharmacokinetics of XN (Nookandeh et al., 2004; Legette et al., 2012, 2014). Investigations using human liver microsomes showed that the hydroxylation of a prenyl methyl group is the primary route of the oxidative metabolism. Furthermore, XN and its metabolites were found to be excreted mainly in feces within 24 h of administration, when XN was fed to rats up to a dose of 500 mg/kg BW (Avula et al., 2004; Hanske et al., 2010). Twenty two metabolites were identified in the feces, most of them confined to modified chalcone structures and flavanone derivatives (Nookandeh et al., 2004). Still, most of the XN remained unchanged in the intestinal tract (89%), and only 11% were found to be metabolites (Nookandeh et al., 2004). Furthermore, two phase I metabolites and five phase II metabolites were identified in rats revealing oxidation, demethylation, hydration and sulfatation reactions (Jirasko et al., 2010). The bioavailability of XN in rats was found to be dose-dependent (0.33, 0.13, and 0.11) upon oral administration of single XN doses (1.86, 5.64, and 16.9 mg/kg BW) (Legette et al., 2012).
Despite the poor bioavailability, the highest XN concentrations are reached in intestinal cells and non-parenchymal liver cells upon oral uptake. Here, the anatomical situation of the liver has to be considered. Thus, it can be expected, that after oral intake of XN its concentration in the portal vein is higher than in the systemic circulation. Further, HSC are located in the liver in the space of Disse (perisinusoidal space), i.e., between the sinusoids and the hepatocytes. Herewith, HSC are directly exposed to XN concentration reaching the liver via the portal vein irrespective of the (subsequent) metabolism in hepatocytes. Anti-fibrogenic effects have been observed at concentrations as low as 5 μM (Dorn et al., 2010a), and in previous studies we found that these concentration levels are reached in the murine hepatic tissue upon oral administration of XN at dose of 1000 mg/kg BW (Dorn et al., 2013). Furthermore, it has to be considered that XN concentrations reaching HSC in the space between the endothelial cells and the hepatocytes (i.e., space of Disse) likely are significantly higher than the levels in whole liver tissue.
Still, the applied dose of 1000 mg/kg BW in this study (Dorn et al., 2013) was quite high and it has not yet been exactly defined what XN doses are required to achieve hepatoprotective effects. In the above described studies revealing beneficial effects in models of acute and chronic liver injury, XN was applied in the dose-range of approximately 100–1000 mg XN/kg BW to mice and rats. Effective doses with regards to beneficial effects on other components of the metabolic syndrome were achieved with doses in the range of 15–300 mg XN /kg BW in rats and mice (Doddapattar et al., 2013; Legette et al., 2013; Yang et al., 2013; Yui et al., 2014). In addition, there are several further studies in other experimental disease models, which revealed beneficial effects in doses as low as 0.2–9 mg XN/kg BW (Benelli et al., 2012; Negrao et al., 2012; Rudzitis-Auth et al., 2012; Yen et al., 2012; Costa et al., 2013). For example, Costa et al. have shown that XN modulates inflammation, oxidative stress, and angiogenesis in a type 1 diabetic rat skin wound healing model by supplementing a stout beer with 10 mg XN/L, which corresponds to approximately 1 mg XN/kg BW/day (Costa et al., 2013). Moreover, Benelli et al. reported that XN revealed beneficial effects in a murine model of leukemia in doses as low as 2 mg XN/kg BW (Benelli et al., 2012).
Potential Forms of XN Application
Elegant studies by Legette et al. (2012) demonstrated the similarity of XN metabolisms and pharmacokinetics between rodents and humans, which allows the translation of data generated in murine and rat models into clinical studies/application. To convert an animal dose (mg/kg BW) to the human equivalent dose (HED), the murine dose should be either divided by 12.3 or multiplied by 0.08. Oral dose ratio can be calculated using allometric interspecies scaling 1.
For humans, beer is the major dietary source of XN. The beer content of XN varies significantly depending on the type of beer (in the range of 0.052–0.628 mg/l) (Chen et al., 2010). Lager and Pilsener beers have fairly low levels of this compound, and the highest levels of XN are found in Stout or Porte (Stevens et al., 1999). Moreover, it was possible to produce a dark beer enriched in XN (3.5 mg/l) (Magalhães et al., 2008), and a brewing process has been developed that produces a beer that contains 10 times the amount of XN as traditional brews (Wunderlich et al., 2005). Even upon consumption of such special types of beer, a daily beer consumption of approximately 150–1500 l would be necessary by a man (75 kg) to reach doses corresponding to 100–1000 mg XN/kg BW/day in mice, i.e., doses which have been shown to exhibit hepatoprotective effects. Thus, with regards to hepatoprotective effects, pharmacologically relevant XN concentrations cannot be reached in men by beer consumption. Moreover, there is certainly unanimous hesitancy among researchers to recommend drinking alcohol to avoid any kind of disease because of the fine line between moderate and binge drinking. Certainly, this is even more true in case of chronic liver disease.
However, XN can also be isolated from hops in large quantities, and different methods (e.g., extraction via liquid supercritical carbon dioxide) were developed to isolate XN from hop cones in large quantities. Thus, independent of beer intake, XN may be used as hepatoprotective dietary supplement. Therefore, pharmacological relevant concentrations can be reached by oral administration of XN enriched functional food, e.g., XN enriched beverages or solid foods. Methods or formulations for increasing the water solubility and bioavailability are presently object of numerous national or global patents2).
Safety of XN Application
One prerequisite for therapeutic application is the good safety profile of the used agent. Especially hepatotoxic properties have to be excluded, when the therapeutic agent must be taken by patients with liver disease. Hop has a long history as a medicinal plant and is known for its good tolerance. More recently, we and others have confirmed the safety of oral application of XN and XN-enriched hop extracts in rats and mice. Oral administration of XN (700 mg/kg/day BW) to mice for 4 weeks did neither affect the major organ functions, nor the protein, lipid, or carbohydrate metabolism (Vanhoecke et al., 2005). Similarly, mice fed with a XN enriched diet (1000 mg/kg BW) for 3 weeks exhibited no adverse effects (Dorn et al., 2010a). Histopathological evaluation of major organs (liver, kidney, colon, lung, heart, spleen, and thymus) as well as biochemical serum analysis, confirmed that XN did not negatively affect organ function and homoeostasis (Dorn et al., 2010c). Most recently, first in man studies confirmed the safety and good tolerability of XN or XN-enriched hop extracts, respectively. An escalating dose study (up to 1.35 mg XN/kg BW/day for 1 week) in menopausal women revealed that the XN enriched extract did neither affect the serum levels of sex hormones nor blood clotting. Also no other side effects were observed (van Breemen et al., 2014). A further study confirmed the safety of oral administration of a single XN dose (160 mg, i.e., approximately 2.5 mg XN/kg BW/day) in healthy volunteers (Legette et al., 2014).
Summary and Conclusion
In vitro and in vivo data indicate that the hop constituent xanthohumol (XN) affects several critical pathophysiological steps during the development and course of chronic liver disease, including hepatic inflammation and fibrosis, as well as the formation and progression of liver cancer (Figure 4). Also on the molecular level, XN ameliorates several mechanisms which play a critical role in the pathogenesis of acute and chronic liver injury. Strikingly, inhibitory XN effects on activated hepatic stellate cells (HSC)/myofibrobasts take place in a concentration range, which is significantly lower than the concentration which is shown to be safe for primary human hepatocytes in vitro. Furthermore, upon oral application, HSC are exposed to relatively high XN concentrations due to their location in the space of Disse irrespective of the hepatic metabolisms. This indicates these non-parenchymal liver cells as attractive targets for therapeutic XN application. Of note, XN also holds promise as a therapeutic agent for treating obesity, dysregulation of glucose metabolism and other components of the metabolic syndrome including hepatic steatosis. Thus, therapeutic XN application appears as promising strategy, particularly in obese patients, to inhibit the development as well as the progression of NAFLD.
Figure 4. Xanthohumol effects on different pathophysiological factors during the course of non-alcoholic fatty liver disease. Xanthohumol (XN) has the potential to inhibit hepatic steatosis, inflammation, fibrosis and even the causes of liver injury by interaction on different levels, i.e., pathogenesis of steatosis (Dorn et al., 2010a; Doddapattar et al., 2013; Yang et al., 2013; Yui et al., 2014), inflammation (Dorn et al., 2010a, 2013; Yang et al., 2013), fibrosis (Dorn et al., 2010a, 2013; Yang et al., 2013), and cancerogenesis (Gerhauser et al., 2002; Dorn et al., 2010b).
Conflict of Interest Statement
Part of the xanthohumol-related research projects from Claus Hellerbrand are funded by Flaxan, a subsidiary of Joh. Barth and Sohn GmbH (Nuremberg, Germany), and by “Wissenschaftsförderung der Deutschen Brauwirtschaft e.V.” (Berlin, Germany). Claus Hellerbrand is a consultant for Flaxan, and Abdo Mahli is working in the laboratory of Claus Hellerbrand. Ralf Weiskirchen and Sabine Weiskirchen have nothing to declare.
We want to thank Dr. Michael Saugspier for providing photographical images of hop plants shown in Figure 1. This work was supported in part by unrestricted research grants from Flaxan, a subsidiary of Joh. Barth and Sohn GmbH (Nuremberg, Germany). Furthermore, this work was supported by “Wissenschaftsförderung der Deutschen Brauwirtschaft e.V.” (Berlin, Germany) (Project No R 437). RW is supported by the German Research Foundation (SFB/TRR57 P13).
BW, body weight; ECM, extracellular matrix; HCC, hepatocellular carcinoma; HCV, hepatitis C virus; HSC, hepatic stellate cells; IFN, interferon; MS, metabolic syndrome; NF-κB, nuclear factor-κB; XN, xanthohumol.
1. ^Guidance for Industry, Estimating the maximum safe starting dose in initial clinical trials for therapeutics in adult healthy volunteers. This guidance can be downloaded at http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM078932.pdf (last downloaded March 20, 2015).
2. ^International application published under the patent cooperation treaty (PCT). A representative example can be downloaded at http://www.lens.org/images/patent/WO/2007016578/A2/WO_2007_016578_A2.pdf (last downloaded March 20, 2015).
Albini, A., Dell'Eva, R., Vene, R., Ferrari, N., Buhler, D. R., Noonan, D. M., et al. (2006). Mechanisms of the antiangiogenic activity by the hop flavonoid xanthohumol: NF-kappaB and Akt as targets. FASEB J. 20, 527–529.
Amann, T., Bataille, F., Spruss, T., Muhlbauer, M., Gabele, E., Scholmerich, J., et al. (2009). Activated hepatic stellate cells promote tumorigenicity of hepatocellular carcinoma. Cancer Sci. 100, 646–653. doi: 10.1111/j.1349-7006.2009.01087.x
Avula, B., Ganzera, M., Warnick, J. E., Feltenstein, M. W., Sufka, K. J., and Khan, I. A. (2004). High-performance liquid chromatographic determination of xanthohumol in rat plasma, urine, and fecal samples. J. Chromatogr. Sci. 42, 378–382. doi: 10.1093/chromsci/42.7.378
Benelli, R., Vene, R., Ciarlo, M., Carlone, S., Barbieri, O., and Ferrari, N. (2012). The AKT/NF-kappaB inhibitor xanthohumol is a potent anti-lymphocytic leukemia drug overcoming chemoresistance and cell infiltration. Biochem. Pharmacol. 83, 1634–1642. doi: 10.1016/j.bcp.2012.03.006
Buckwold, V. E., Wilson, R. J., Nalca, A., Beer, B. B., Voss, T. G., Turpin, J. A., et al. (2004). Antiviral activity of hop constituents against a series of DNA and RNA viruses. Antiviral Res. 61, 57–62. doi: 10.1016/S0166-3542(03)00155-4
Chen, L., Zhao, Q., Jin, H., Zhang, X., Xu, Y., Yu, A., et al. (2010). Determination of xanthohumol in beer based on cloud point extraction coupled with high performance liquid chromatography. Talanta 81, 692–697. doi: 10.1016/j.talanta.2010.01.004
Colgate, E. C., Miranda, C. L., Stevens, J. F., Bray, T. M., and Ho, E. (2007). Xanthohumol, a prenylflavonoid derived from hops induces apoptosis and inhibits NF-kappaB activation in prostate epithelial cells. Cancer Lett. 246, 201–209. doi: 10.1016/j.canlet.2006.02.015
Costa, R., Negrao, R., Valente, I., Castela, A., Duarte, D., Guardao, L., et al. (2013). Xanthohumol modulates inflammation, oxidative stress, and angiogenesis in type 1 diabetic rat skin wound healing. J. Nat. Prod. 76, 2047–2053. doi: 10.1021/np4002898
Dietz, B. M., Hagos, G. K., Eskra, J. N., Wijewickrama, G. T., Anderson, J. R., Nikolic, D., et al. (2013). Differential regulation of detoxification enzymes in hepatic and mammary tissue by hops (Humulus lupulus) in vitro and in vivo. Mol. Nutr. Food Res. 57, 1055–1066. doi: 10.1002/mnfr.201200534
Doddapattar, P., Radovic, B., Patankar, J. V., Obrowsky, S., Jandl, K., Nusshold, C., et al. (2013). Xanthohumol ameliorates atherosclerotic plaque formation, hypercholesterolemia, and hepatic steatosis in ApoE-deficient mice. Mol. Nutr. Food Res. 57, 1718–1728. doi: 10.1002/mnfr.201200794
Dorn, C., Bataille, F., Gaebele, E., Heilmann, J., and Hellerbrand, C. (2010c). Xanthohumol feeding does not impair organ function and homoeostasis in mice. Food Chem. Toxicol. 48, 1890–1897. doi: 10.1016/j.fct.2010.04.030
Dorn, C., Kraus, B., Motyl, M., Weiss, T. S., Gehrig, M., Scholmerich, J., et al. (2010a). Xanthohumol, a chalcon derived from hops, inhibits hepatic inflammation and fibrosis. Mol. Nutr. Food Res. 54(Suppl. 2), S205–S213. doi: 10.1002/mnfr.200900314
Dorn, C., Massinger, S., Wuzik, A., Heilmann, J., and Hellerbrand, C. (2013). Xanthohumol suppresses inflammatory response to warm ischemia-reperfusion induced liver injury. Exp. Mol. Pathol. 94, 10–16. doi: 10.1016/j.yexmp.2012.05.003
Dorn, C., Weiss, T. S., Heilmann, J., and Hellerbrand, C. (2010b). Xanthohumol, a prenylated chalcone derived from hops, inhibits proliferation, migration and interleukin-8 expression of hepatocellular carcinoma cells. Int. J. Oncol. 36, 435–441. doi: 10.1055/s-0029-1246396
Douhara, A., Moriya, K., Yoshiji, H., Noguchi, R., Namisaki, T., Kitade, M., et al. (2015). Reduction of endotoxin attenuates liver fibrosis through suppression of hepatic stellate cell activation and remission of intestinal permeability in a rat non-alcoholic steatohepatitis model. Mol. Med. Rep. 11, 1693–1700. doi: 10.3892/mmr.2014.2995
Ferk, F., Huber, W. W., Filipic, M., Bichler, J., Haslinger, E., Misík, M., et al. (2010). Xanthohumol, a prenylated flavonoid contained in beer, prevents the induction of preneoplastic lesions and DNA damage in liver and colon induced by the heterocyclic aromatic amine amino-3-methyl-imidazo[4,5-f]quinoline (IQ). Mutat. Res. 691, 17–22. doi: 10.1016/j.mrfmmm.2010.06.006
Gerhauser, C. (2005). Broad spectrum anti-infective potential of xanthohumol from hop (Humulus lupulus L.) in comparison with activities of other hop constituents and xanthohumol metabolites. Mol. Nutr. Food Res. 49, 827–831. doi: 10.1002/mnfr.200500091
Gerhauser, C., Alt, A., Heiss, E., Gamal-Eldeen, A., Klimo, K., Knauft, J., et al. (2002). Cancer chemopreventive activity of Xanthohumol, a natural product derived from hop. Mol. Cancer Ther. 1, 959–969.
Hanske, L., Loh, G., Sczesny, S., Blaut, M., and Braune, A. (2010). Recovery and metabolism of xanthohumol in germ-free and human microbiota-associated rats. Mol. Nutr. Food Res. 54, 1405–1413. doi: 10.1002/mnfr.200900517
Hartkorn, A., Hoffmann, F., Ajamieh, H., Vogel, S., Heilmann, J., Gerbes, A. L., et al. (2009). Antioxidant effects of xanthohumol and functional impact on hepatic ischemia-reperfusion injury. J. Nat. Prod. 72, 1741–1747. doi: 10.1021/np900230p
Hellerbrand, C., Jobin, C., Iimuro, Y., Licato, L., Sartor, R. B., and Brenner, D. A. (1998a). Inhibition of NFkappaB in activated rat hepatic stellate cells by proteasome inhibitors and an IkappaB super-repressor. Hepatology 27, 1285–1295. doi: 10.1002/hep.510270514
Hellerbrand, C., Jobin, C., Licato, L. L., Sartor, R. B., and Brenner, D. A. (1998b). Cytokines induce NF-kappaB in activated but not in quiescent rat hepatic stellate cells. Am. J. Physiol. 275(2 Pt 1), G269–G278.
Henderson, M. C., Miranda, C. L., Stevens, J. F., Deinzer, M. L., and Buhler, D. R. (2000). In vitro inhibition of human P450 enzymes by prenylated flavonoids from hops, Humulus lupulus. Xenobiotica 30, 235–251. doi: 10.1080/004982500237631
Huh, C. G., Factor, V. M., Sanchez, A., Uchida, K., Conner, E. A., and Thorgeirsson, SS. (2004). Hepatocyte growth factor/c-met signaling pathway is required for efficient liver regeneration and repair. Proc. Natl. Acad. Sci. U.S.A. 101, 4477–4482. doi: 10.1073/pnas.0306068101
Jaeschke, H., Schini, V. B., and Farhood, A. (1992). Role of nitric oxide in the oxidant stress during ischemia/reperfusion injury of the liver. Life Sci. 50, 1797–1804. doi: 10.1016/0024-3205(92)90064-V
Jarrar, M. H., Baranova, A., Collantes, R., Ranard, B., Stepanova, M., Bennett, C., et al. (2008). Adipokines and cytokines in non-alcoholic fatty liver disease. Aliment. Pharmacol. Ther. 27, 412–421. doi: 10.1111/j.1365-2036.2007.03586.x
Jirasko, R., Holcapek, M., Vrublova, E., Ulrichova, J., and Simanek, V. (2010). Identification of new phase II metabolites of xanthohumol in rat in vivo biotransformation of hop extracts using high-performance liquid chromatography electrospray ionization tandem mass spectrometry. J. Chromatogr. A 1217, 4100–4108. doi: 10.1016/j.chroma.2010.02.041
Jongthawin, J., Techasen, A., Loilome, W., Yongvanit, P., and Namwat, N. (2012). Anti-inflammatory agents suppress the prostaglandin E2 production and migration ability of cholangiocarcinoma cell lines. Asian Pac. J. Cancer Prev. 13(Suppl.), 47–51.
Kisseleva, T., and Brenner, D. A. (2007). Role of hepatic stellate cells in fibrogenesis and the reversal of fibrosis. J. Gastroenterol. Hepatol. 22(Suppl. 1), S73–S78. doi: 10.1111/j.1440-1746.2006.04658.x
Krajka-Kuzniak, V., Paluszczak, J., and Baer-Dubowska, W. (2013). Xanthohumol induces phase II enzymes via Nrf2 in human hepatocytes in vitro. Toxicol. In Vitro. 27, 149–156. doi: 10.1016/j.tiv.2012.10.008
Kramer, B., Thielmann, J., Hickisch, A., Muranyi, P., Wunderlich, J., and Hauser, C. (2015). Antimicrobial activity of hop extracts against foodborne pathogens for meat applications. J. Appl. Microbiol. 118, 648–657. doi: 10.1111/jam.12717
Legette, L., Karnpracha, C., Reed, R. L., Choi, J., Bobe, G., Christensen, J. M., et al. (2014). Human pharmacokinetics of xanthohumol, an antihyperglycemic flavonoid from hops. Mol. Nutr. Food Res. 58, 248–255. doi: 10.1002/mnfr.201300333
Legette, L., Ma, L., Reed, R. L., Miranda, C. L., Christensen, J. M., Rodriguez-Proteau, R., et al. (2012). Pharmacokinetics of xanthohumol and metabolites in rats after oral and intravenous administration. Mol. Nutr. Food Res. 56, 466–474. doi: 10.1002/mnfr.201100554
Legette, L. L., Luna, A. Y., Reed, R. L., Miranda, C. L., Bobe, G., Proteau, R. R., et al. (2013). Xanthohumol lowers body weight and fasting plasma glucose in obese male Zucker fa/fa rats. Phytochemistry 91, 236–241. doi: 10.1016/j.phytochem.2012.04.018
Lou, S., Zheng, Y. M., Liu, S. L., Qiu, J., Han, Q., Li, N., et al. (2014). Inhibition of hepatitis C virus replication in vitro by xanthohumol, a natural product present in hops. Planta Med. 80, 171–176.
Magalhães, P. J., Dostalek, P., Cruz, J. M., Guido Ls, F, and Barros, A. A. (2008). The impact of a xanthohumol-enriched hop product on the behavior of xanthohumol and isoxanthohumol in pale and dark beers: a pilot scale approach. J. Inst. Brewing 114, 246–256. doi: 10.1002/j.2050-0416.2008.tb00335.x
Minguez, B., Tovar, V., Chiang, D., Villanueva, A., and Llovet, J. M. (2009). Pathogenesis of hepatocellular carcinoma and molecular therapies. Curr. Opin. Gastroenterol. 25, 186–194. doi: 10.1097/MOG.0b013e32832962a1
Miranda, C. L., Aponso, G. L., Stevens, J. F., Deinzer, M. L., and Buhler, D. R. (2000a). Prenylated chalcones and flavanones as inducers of quinone reductase in mouse Hepa 1c1c7 cells. Cancer Lett. 149, 21–29. doi: 10.1016/S0304-3835(99)00328-6
Miranda, C. L., Stevens, J. F., Ivanov, V., McCall, M., Frei, B., Deinzer, M. L., et al. (2000b). Antioxidant and prooxidant actions of prenylated and nonprenylated chalcones and flavanones in vitro. J. Agric. Food Chem. 48, 3876–3884. doi: 10.1021/jf0002995
Miranda, C. L., Yang, Y. H., Henderson, M. C., Stevens, J. F., Santana-Rios, G., Deinzer, M. L., et al. (2000c). Prenylflavonoids from hops inhibit the metabolic activation of the carcinogenic heterocyclic amine 2-amino-3-methylimidazo[4, 5-f]quinoline, mediated by cDNA-expressed human CYP1A2. Drug Metab. Dispos. 28, 1297–1302.
Monteiro, R., Becker, H., Azevedo, I., and Calhau, C. (2006). Effect of hop (Humulus lupulus L.) flavonoids on aromatase (estrogen synthase) activity. J. Agric. Food Chem. 54, 2938–2943. doi: 10.1021/jf053162t
Negrao, R., Costa, R., Duarte, D., Gomes, T. T., Coelho, P., Guimaraes, J. T., et al. (2012). Xanthohumol-supplemented beer modulates angiogenesis and inflammation in a skin wound healing model. Involvement of local adipocytes. J. Cell. Biochem. 113, 100–109. doi: 10.1002/jcb.23332
Nookandeh, A., Frank, N., Steiner, F., Ellinger, R., Schneider, B., Gerhauser, C., et al. (2004). Xanthohumol metabolites in faeces of rats. Phytochemistry 65, 561–570. doi: 10.1016/j.phytochem.2003.11.016
Pan, L., Becker, H., and Gerhauser, C. (2005). Xanthohumol induces apoptosis in cultured 40-16 human colon cancer cells by activation of the death receptor- and mitochondrial pathway. Mol. Nutr. Food Res. 49, 837–843. doi: 10.1002/mnfr.200500065
Pinto, C., Duque, A. L., Rodríguez-Galdón, B., Cestero, J. J., Macías, P. (2012). Xanthohumol prevents carbon tetrachloride-induced acute liver injury in rats. Food Chem. Toxicol. 50, 3405–3412. doi: 10.1016/j.fct.2012.07.035
Plazar, J., Zegura, B., Lah, T. T., and Filipic, M. (2007). Protective effects of xanthohumol against the genotoxicity of benzo(a)pyrene (BaP), 2-amino-3-methylimidazo[4,5-f]quinoline (IQ) and tert-butyl hydroperoxide (t-BOOH) in HepG2 human hepatoma cells. Mutat. Res. 632, 1–8. doi: 10.1016/j.mrgentox.2007.03.013
Possemiers, S., Heyerick, A., Robbens, V., De Keukeleire, D., and Verstraete, W. (2005). Activation of proestrogens from hops (Humulus lupulus L.) by intestinal microbiota; conversion of isoxanthohumol into 8-prenylnaringenin. J. Agric. Food Chem. 53, 6281–6288. doi: 10.1021/jf0509714
Rauen, U., Viebahn, R., Lauchart, W., and de Groot, H. (1994). The potential role of reactive oxygen species in liver ischemia/reperfusion injury following liver surgery. Hepatogastroenterology 41, 333–336.
Rozalski, M., Micota, B., Sadowska, B., Stochmal, A., Jedrejek, D., Wieckowska-Szakiel, M., et al. (2013). Antiadherent and antibiofilm activity of Humulus lupulus L. derived products: new pharmacological properties. Biomed. Res. Int. 2013:101089. doi: 10.1155/2013/101089
Rudzitis-Auth, J., Korbel, C., Scheuer, C., Menger, M. D., and Laschke, M. W. (2012). Xanthohumol inhibits growth and vascularization of developing endometriotic lesions. Hum. Reprod. 27, 1735–1744. doi: 10.1093/humrep/des095
Saidijam, M., Tootoonchi, A. S., Goodarzi, M. T., Hassanzadeh, T., Borzuei, S. H., Yadegarazari, R., et al. (2014). Expression of interleukins 7 & 8 in peripheral blood mononuclear cells from patients with metabolic syndrome: a preliminary study. Indian J. Med. Res. 140, 238–243.
Shamoto, T., Matsuo, Y., Shibata, T., Tsuboi, K., Takahashi, H., Funahashi, H., et al. (2013). Xanthohumol inhibits angiogenesis through VEGF and IL-8 in pancreatic cancer. Pancreatology 13, S52–S53. doi: 10.1016/j.pan.2013.07.203
Stevens, J. F., Taylor, A. W., and Deinzer, M. L. (1999). Quantitative analysis of xanthohumol and related prenylflavonoids in hops and beer by liquid chromatography-tandem mass spectrometry. J. Chromatogr. A 832, 97–107. doi: 10.1016/S0021-9673(98)01001-2
van Breemen, R. B., Yuan, Y., Banuvar, S., Shulman, L. P., Qiu, X., Alvarenga, R. F., et al. (2014). Pharmacokinetics of prenylated hop phenols in women following oral administration of a standardized extract of hops. Mol. Nutr. Food Res. 58, 1962–1969. doi: 10.1002/mnfr.201400245
Vanhoecke, B. W., Delporte, F., Van, B. E., Heyerick, A., Depypere, H. T., Nuytinck, M., et al. (2005). A safety study of oral tangeretin and xanthohumol administration to laboratory mice. In Vivo 19, 103–107.
Vernon, G., Baranova, A., and Younossi, Z. M. (2011). Systematic review: the epidemiology and natural history of non-alcoholic fatty liver disease and non-alcoholic steatohepatitis in adults. Aliment. Pharmacol. Ther. 34, 274–285. doi: 10.1111/j.1365-2036.2011.04724.x
Viegas, O., Zegura, B., Pezdric, M., Novak, M., Ferreira, I. M., Pinho, O., et al. (2012). Protective effects of xanthohumol against the genotoxicity of heterocyclic aromatic amines MeIQx and PhIP in bacteria and in human hepatoma (HepG2) cells. Food Chem. Toxicol. 50, 949–955. doi: 10.1016/j.fct.2011.11.031
Villanueva, A., Newell, P., Chiang, D. Y., Friedman, S. L., and Llovet, J. M. (2007). Genomics and signaling pathways in hepatocellular carcinoma. Semin. Liver Dis. 27, 55–76. doi: 10.1055/s-2006-960171
Wouters, K., van Gorp, P. J., Bieghs, V., Gijbels, M. J., Duimel, H., Lutjohann, D., et al. (2008). Dietary cholesterol, rather than liver steatosis, leads to hepatic inflammation in hyperlipidemic mouse models of nonalcoholic steatohepatitis. Hepatology 48, 474–486. doi: 10.1002/hep.22363
Yang, M., Li, N., Li, F., Zhu, Q., Liu, X., Han, Q., et al. (2013). Xanthohumol, a main prenylated chalcone from hops, reduces liver damage and modulates oxidative reaction and apoptosis in hepatitis C virus infected Tupaia belangeri. Int. Immunopharmacol. 16, 466–474. doi: 10.1016/j.intimp.2013.04.029
Yen, T. L., Hsu, C. K., Lu, W. J., Hsieh, C. Y., Hsiao, G., Chou, D. S., et al. (2012). Neuroprotective effects of xanthohumol, a prenylated flavonoid from hops (Humulus lupulus), in ischemic stroke of rats. J. Agric. Food Chem. 60, 1937–1944. doi: 10.1021/jf204909p
Yoshimaru, T., Komatsu, M., Tashiro, E., Imoto, M., Osada, H., Miyoshi, Y., et al. (2014). Xanthohumol suppresses oestrogen-signalling in breast cancer through the inhibition of BIG3-PHB2 interactions. Sci. Rep. 4, 7355. doi: 10.1038/srep07355
Zhang, N., Liu, Z., Han, Q., Chen, J., Lou, S., Qiu, J., et al. (2009). Inhibition of bovine viral diarrhea virus in vitro by xanthohumol: comparisons with ribavirin and interferon-alpha and implications for the development of anti-hepatitis C virus agents. Eur. J. Pharm. Sci. 38, 332–340. doi: 10.1016/j.ejps.2009.08.005
Zhang, N., Liu, Z., Han, Q., Chen, J., and Lv, Y. (2010). Xanthohumol enhances antiviral effect of interferon alpha-2b against bovine viral diarrhea virus, a surrogate of hepatitis C virus. Phytomedicine 17, 310–316. doi: 10.1016/j.phymed.2009.08.005
Keywords: xanthohumol, hops, fibrosis, hepatic stellate cells, liver disease
Citation: Weiskirchen R, Mahli A, Weiskirchen S and Hellerbrand C (2015) The hop constituent xanthohumol exhibits hepatoprotective effects and inhibits the activation of hepatic stellate cells at different levels. Front. Physiol. 6:140. doi: 10.3389/fphys.2015.00140
Received: 21 March 2015; Accepted: 20 April 2015;
Published: 06 May 2015.
Edited by:Ali Canbay, University Hospital Essen, Germany
Reviewed by:Wing-Kin Syn, The Institute of Hepatology, UK
Heike Bantel, Hannover Medical School, Germany
Copyright © 2015 Weiskirchen, Mahli, Weiskirchen and Hellerbrand. 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) or licensor 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.
*Correspondence: Claus Hellerbrand, Department of Internal Medicine I, University Hospital Regensburg, Franz-Josef-Strauss-Allee 11, D-93053 Regensburg, Germany, email@example.com
†These authors have contributed equally to this work.