Abstract
The sinoatrial node (SAN) is composed of highly specialized cells that mandate the spontaneous beating of the heart through self-generation of an action potential (AP). Despite this automaticity, the SAN is under the modulation of the autonomic nervous system (ANS). In diabetes mellitus (DM), heart rate variability (HRV) manifests as a hallmark of diabetic cardiomyopathy. This is paralleled by an impaired regulation of the ANS, and by a pathological remodeling of the pacemaker structure and function. The direct effect of diabetes on the molecular signatures underscoring this pathology remains ill-defined. The recent focus on the electrical currents of the SAN in diabetes revealed a repressed firing rate of the AP and an elongation of its tracing, along with conduction abnormalities and contractile failure. These changes are blamed on the decreased expression of ion transporters and cell-cell communication ports at the SAN (i.e., HCN4, calcium and potassium channels, connexins 40, 45, and 46) which further promotes arrhythmias. Molecular analysis crystallized the RGS4 (regulator of potassium currents), mitochondrial thioredoxin-2 (reactive oxygen species; ROS scavenger), and the calcium-dependent calmodulin kinase II (CaMKII) as metabolic culprits of relaying the pathological remodeling of the SAN cells (SANCs) structure and function. A special attention is given to the oxidation of CaMKII and the generation of ROS that induce cell damage and apoptosis of diabetic SANCs. Consequently, the diabetic SAN contains a reduced number of cells with significant infiltration of fibrotic tissues that further delay the conduction of the AP between the SANCs. Failure of a genuine generation of AP and conduction of their derivative waves to the neighboring atrial myocardium may also occur as a result of the anti-diabetic regiment (both acute and/or chronic treatments). All together, these changes pose a challenge in the field of cardiology and call for further investigations to understand the etiology of the structural/functional remodeling of the SANCs in diabetes. Such an understanding may lead to more adequate therapies that can optimize glycemic control and improve health-related outcomes in patients with diabetes.
1 The Sinoatrial Node as a Pacemaker of the Heart
Cardiac rhythm is controlled by the activity of a heterogeneous collection of highly specialized cells forming the SAN, located at the wall (epicardium) of the right atrium, laterally to the entrance of the superior vena cava, and in the vicinity to the cristae terminalis (, ). Since its discovery about a century ago (1907) by Arthur Keith and Martin Flack, the SAN has attracted the attention of scientists to decipher its characteristics ().
The length of the SAN ranges from 8-21.5 mm, comprising the head, the central area and the tail (, ). Optical mapping techniques identified several spots, within the SAN, that discharge action potentials (APs), ultimately leading to the depolarization of the atrial muscle (). The unique electrophysiological properties of the SAN cells (SANCs) are conducive to self-excitation yielding spontaneous depolarization, thus pacemaker activity, in the absence of external stimuli (). This is mandated by the ingress of sodium (funny current) and calcium ions through the sarcolemma () which constantly lifts up the unstable resting membrane potential (~ 60 mV) of SANCs towards the threshold (~ -40 mV), before the upstroke of the AP arises (, ). Despite this, the self-excitation process per se is insufficient; it still requires a special cellular organization/structure that promotes the exit of the AP throughout well-defined pathways to spread through, and efficiently depolarize the adjacent myocardium (left atrium) (). These include a remarkable cell-cell communication profile implicating low conductance gap junctions with a particular transmission pattern of the electrical signals, along with an electrical insulator (connective tissue) surrounding the grouped SANCs (). The connective tissue is needed to avoid the random dissipation of the depolarization wave and to focus its trajectory through specific exit pathways for an effective propagation of the AP through the atrial myocardium (). The blood supply to the SAN is mainly through the right coronary artery in most cases, to a lesser extent by the circumflex of the left coronary artery, and by both coronary arteries in a very minor portion of the population (–). Therefore, the safety of cardiac rhythm highly hinges on a properly functioning SAN that must be constantly supplied by the appropriate amount of oxygen/nutrients.
2 SAN Cells Lineage and Developmental Changes
SANCs are structurally and functionally different from the surrounding cardiomyocytes (, ). The SAN comprises a collection of weakly connected cells (pacemaker cells, adipocytes, myocytes, and fibroblasts) out of which those defining the pacemaker activity of the node are divided into three main types of cells; the elongated spindle shaped cells (~80 µm in length), the spindle cells (~ 40µm), and the spider-shaped cells [reviewed in ()]. A careful inspection of human SAN revealed the presence of mainly three different types of cells: the pale (P) cells organized in clusters with elongated cytoplasmic extensions, the transitional (T) cells that resemble cardiomyocytes but with fewer sarcomeres, and the fibroblast-like cells with long bi-tripolar contacting cells (). All together, these cells are insulated by fibrous tissues from the rest of the atrial myocardium. This insulation shields the SANCs from atrial hyperpolarization and provides a unidirectional route for the depolarization wave initiated at the SAN center to spread in mainly three directions (outside the superior vena cava, outside the inferior vena cava, and between both venae cava) and therefore to invade the atrial muscle (). Despite the heterogeneity of these cells, along with the difference in their distribution across the SAN (cristae terminals vs atrial septum), there are unifying active electrical properties at the plasma membrane that support the pacing activity under normal circumstances. At the initial stages of cardiac development, all cardiac cells possess pacemaker activity, however, the majority develop into working myocardium and few cells form the conduction system of the heart (SAN, Atrioventricular node, and His-Purkinje fibers). This is achieved by localized and targeted repression of differentiation of specific genes that drive these cells into cardiac muscle via an interplay between different modulators of the transcription (example: Tbx5, Nkx-5, Tbx-2, Tb-3, and Id2) (). A primordium SAN is shown as early as Embryonic (E) day 10.5 in mouse hearts (). At this stage, SANCs are relatively poor in organelles and myofibrils compared to the other cardiomyocytes at E16 and E18 in mice, and they are characterized by a strikingly poor proliferative capacity at embryonic levels (compared with cardiomyocytes) (). At birth, the pacing of the SAN overrides all other parts of the conduction system (Atrioventricular node and His-Purkinje fibers) and guarantees a heart rate of about 70-90 beats per min in healthy subjects. Heart rate variability (HRV) is tightly linked to changes in the activity of the SAN (intrinsic or extrinsic factors). With age, the decrease in the volume of nodal cells and SAN tissues, along with the development of fibrosis can result in dysfunction of the SAN (, ).
3 Regulation of SAN by the Autonomic Nervous System and the Coupled-Clock System
Under physiological conditions, HRV is regulated by two main signaling cascades: the autonomic nervous system (ANS) and the coupled-clock system within the SANCs (). The involvement of the ANS implicates the brain as a modulator of the SANCs automaticity through a balanced control of G-protein-coupled receptors (GPCRs) from both ANS branches: the sympathetic and the parasympathetic nervous system (SNS and PNS). Stimulation of the sympathetic nervous system (SNS) increases HR while stimulation of the parasympathetic nervous system (PNS) decreases the HR (, ). Acetylcholine that is released upon PNS stimulation acts on muscarinic receptors (M2R) in the SAN of the human heart and reduces its rate of firing ().
The sympathetic activation of the heart (adrenergic), via the release of its neurotransmitter norepinephrine (NE), leads to the activation of the β-adrenergic receptors (β-AR) expressed at the sarcolemma of SANCs, thus causing the activation of the β-AR cyclase. The β-AR pathway involves the activation of adenylyl cyclase (AC), via the stimulatory guanosine triphosphate (GTP) regulatory protein (Gs), which converts adenosine triphosphate (ATP) into adenosine 3′, 5′- monophosphate (cAMP), which in turn stimulates cAMP-dependent protein kinase A (PKA) (). PKA is a central mediator of β-AR regulation of cardiac function. Subsequently, a multitude of target proteins including the ryanodine receptors (RyR) and the sarco-/endoplasmic reticulum Ca2+ ATPase (SERCA) Ca2+ pumps in the SAN are phosphorylated by PKA to evoke intracellular Ca2+ [(Ca2+)i] oscillations affecting currents through the Na+/Ca2+ exchanger (NCX) (). This surge of [Ca2+]i ultimately increases the slope of the spontaneous diastolic depolarization (SDD) and consequently the heart rate (HR) (positive chronotropic effect) (). There is increasing evidence that SAN pacemaker activity is subject to an intrinsic regulation by CaMKII via modulation of L-type Ca2+ currents (ICa,L)inactivation and reactivation (, ). Additionally, the hyperpolarization-activated cyclic nucleotide-gated (HCN) channel gene family is a key determinant of mechanisms underlying chronotropic effects of β-AR stimulation (). HCN4 channels are the most prevalent in SAN. These channels are regulated by PKA and therefore they are involved in the auto-pacing activity of SAN, as well as in the autonomic modulation of the HR ().
In contrast, the parasympathetic input represses the rhythm of SANCs through the release of acetylcholine (ACh) which reduces the production of cAMP in SANCs. More importantly, ACh activates the potassium channels driving the SANCs into the hyperpolarized state. This leads to a reduced slope of SDD and a decrease in HR (negative chronotropic effect) (36). Nonetheless, exposure of SAN cells to adrenaline or acetylcholine revealed a shift in the pacemaker locus across the SAN tissues, thus implying a different expression pattern of the effectors/signaling cascades (to these neurotransmitters) by SANCs and reinstating their heterogeneity ().
Although debatable, the “coupled-clock” system is believed to regulate the automaticity of the SANCs (). It comprises an ensemble of highly dynamic membranes: the surface membrane (Sarcolemma-SL) and the sarcoplasmic reticulum (SR) membrane. The SL and SR membranes express ion channels and transporters defining the membrane clock or “M clock” and “Ca2+ clock”. Both clocks work interdependently but synergistically contribute to SDD, triggering the AP upstroke (37). The degree of the coupling between the “M” and the “Ca2+” clocks delineates the normal pacemaker function ().
Electrophysiological studies identified electrical currents that form the pacemaker AP in SANCs. The ionic currents defining the “M clock” include the funny current (If) carried by HCN channel (38), T-type (Cav3.1) calcium current (ICa,T) (39), L-type (Cav1.3 and Cav1.2) calcium currents (ICa,L) (40), sodium-calcium exchange current (INCX) (41), and rapid and slow delayed rectifier potassium currents (IK,r and IK,s) (42, 43). Proteins defining the “Ca2+ clock” include RyR2 (44) and SERCA (45).
In general, local diastolic Ca2+ releases (LCRs) from the SR occur rhythmically. This promotes the Na+/Ca2+ exchange (NCX) current (INCX) to generate a local AP which subsequently spreads as a depolarization wave over the SANCs and the neighboring myocardium (46). It is believed that the Ca2+-cAMP-PKA pathway is also involved in regulating the clock coupling (45). In fact, Ca2+ release stimulates both the CaMKII and PKA via Ca2+-calmodulin activated ACs. These kinases phosphorylate the SL “M clock” proteins and the SR Ca2+ cycling proteins, which promotes SR Ca2+ release, thus further promoting the Ca2+ -calmodulin-activated ACs and CaMKII (). It has been shown that withdrawal of β-AR stimulation uncouples the clocks, thus failing to generate a spontaneous AP in SANCs (45). Recently, Sirenko and colleagues reported that the inhibition of the phosphoprotein phosphatases (PP) increases the firing rate of APs via the coupled-clock mechanism, including respective increases in the SR Ca2+ pumping rate, ICa,L, and INCX (46).
4 SAN Remodeling and Dysfunction in Diabetes
Diabetes mellitus (DM) is a global health problem that affects hundreds of millions of people worldwide (47). The chronic hyperglycemia seen in diabetes is precipitated due to abnormalities in insulin secretion, insulin action, or a combination of both in the form of insulin resistance. The prevalence worldwide ranges from around 5% to more than 15%. In the Middle East, the prevalence is reported to be among the highest in the world, with an average of 11.4% (48). The prevalence of cardiovascular risk factors is high among patients with diabetes and in those with earlier onset of the disease, where higher cardiovascular risks and poorer cardiovascular outcomes and mortality are seen (49). In fact, the leading cause of mortality among patients with diabetes is cardiovascular disease (50). Besides mechanical changes, alteration in the electrical function is another main characteristic of a diabetic heart.
Overall, metabolic abnormalities have been linked to a reduction in sympathetic activity and atypical SAN function (51, 52). This is mainly blamed on nerve growth factor production by adipocytes (53). Such release of growth factors can also account for the higher level of innervation seen in the nodal tissue (53). For example, the adipocyte-derived metabolic hormone leptin has also been suggested to be linked to the SAN function. Leptin receptor-deficient mice are at higher risk of developing arrhythmias due to a reduction in SAN recovery time and relative autonomic denervation (54). The SAN function has also been linked to metabolic changes through the role of free fatty acids (FFA) whereby the If current is upregulated by FFA and sympathetic innervation, which results in increasing intracellular Ca2+ level and Ist current (55, 56). Collectively, these studies demonstrate that diabetes induces metabolism-mediated dysfunction of the SAN.
4.1 Effects of the Impaired Autonomic Nervous System on SAN Function in Diabetic Conditions
One of the most important determinants of cardiac function and performance is the HR, which is modulated by the intrinsic rhythmical firing of the SAN. DM is associated with significant cardiovascular complications and neuropathies (57, 58). The regulation of HR by the ANS has been shown to be impaired in diabetic patients (59, 60). This condition is referred to as cardiovascular autonomic neuropathy (CAN), one of the earliest manifestations of DM (59). Up to 90% of diabetic patients exhibit CAN, which is often accompanied by impairment of the nerves of the heart and possible damage to the PNS mechanisms regulating HR (59, 60). These findings are of crucial clinical significance since DM patients with CAN have increased mortality as compared to patients with DM who do not exhibit CAN (61).
In type 2 DM (T2DM), PNS activity is impaired (59, 62). In addition, in type 1 DM (T1DM), there is an impairment in the mechanisms regulating HR by PNS, and that this impairment is accompanied by a change in the response of the SAN to PNS agonists such as carbachol (CCh) (63, 64). The impaired PNS activity and CAN are demonstrated earlier in T2DM as compared to T1DM (59); however, the mechanisms that are involved in the impaired regulation of HR by PNS in T2DM are not completely understood. It appears that the cardiac autonomic dysfunction that is associated with T2DM is mainly caused by direct damage to the autonomic nerves themselves (59, 65, 66); however, a direct impairment of the SAN function with T2DM cannot be ruled out at this time.
It is important to note that screening diabetic patients for cardiac autonomic neuropathy is highly recommended, especially in those patients with a history of macrovascular or microvascular complications, increased cardiovascular risk, and poor glycemic control (67). While cardiovascular reflex tests are still standard of care, the measurement of HRV is one of the most convenient, pain-free ways to reliably assess the cardiac autonomic neuropathy (68, 69). HRV is defined as the variation between two consecutive heartbeats. A decrease in ANS function has been reported to precede the progression into hypertension (70). Higher HRV indicates higher parasympathetic activity and reflects better adaptations to microenvironmental changes (71), and low HRV is reported as a marker of increased cardiovascular risk (69, 72). Among the general population, increased systolic blood pressure, abdominal diameter, waist–hip ratio, and body mass index (BMI) have been associated with decreased HRV (73, 74). HRV was reported to be improved following weight loss (75). No substantial data is available on the relationship of these parameters in the diabetic state, and the present data on HRV among patients with diabetes is contradictory (76, 77). Nevertheless, it has been reported that HRV is reduced in T1DM youth patients (78).
4.2 Cellular and Molecular Changes Within the Diabetic SAN Tissue
Irrespective of the modality of diabetes (T1DM vs. T2DM), manifestations of the sympathetic and parasympathetic axes certainly precipitate variabilities in cardiac rhythm. Despite this direct modulation of the SAN by the ANS, the cellular, molecular, and structural changes within the SAN tissue in hyperglycemic conditions remain ill-defined.
Spontaneous and rhythmical APs are generated by the SANCs, the primary pacemaker of the heart. Under normal circumstances, these spontaneous APs, and the slow diastolic depolarization between successive APs, contribute to the determination of the intrinsic HR (). The length of time between successive APs in the myocytes of the SAN is determined by the contributions of ionic currents that can affect the transition from the maximum diastolic potential (MDP) to the threshold and the initiation of the next AP. The ionic currents include the hyperpolarization-activated current or funny current (If), and a rapidly activating delayed rectifier K+ currents (IKr) generated by ether-a-go-go (ERG) channels (, , 79). The PNS reduces HR by activation of inhibitory G proteins associated with M2R and attenuating spontaneous firing of AP in SAN myocytes (58). While the primary pacemaker activity of the SAN is spontaneously generated, the rate of this activity and, therefore the HR, can be modified by factors such as ANS, hormones and neurotransmitters, medications, ions, hypoxia, as well as disease states.
In a recent study, Liu et al. (58) examined the effects of carbachol (CCh) on HR and SAN function in isolated SAN cardiomyocytes of male and female db/db mice, an animal model exhibiting features of T2DM. CCh showed an attenuated effect on slowing the spontaneous AP firing which was associated with a smaller decrease in the slope of diastolic depolarization and a reduced hyperpolarization of the MDP. CCh did not produce significant hyperpolarization in SAN cardiomyocytes isolated from male and female db/db mice (58). The results of this study provided some evidence for cellular and molecular mechanisms that might lead to the attenuated regulation of PNS on HR in T2DM (58). The acetylcholine-activated K+ current (IKACh) becomes desensitized and its amplitude diminishes in the presence of an M2R agonist such as CCh (80–82). This channel, IKACh, which mediates the activation of PNS in the SAN, was found to exhibit increased desensitization and faster deactivation kinetics in the SAN of db/db mice, resulting in an attenuated effect of CCh on HR in these mice. Furthermore, the impaired IKACh in SAN myocytes was attributed to altered G protein signaling 4 (RGS4) and phosphatidylinositol (3,4,5) P3 (PIP3) signaling. The authors concluded that their findings may identify new interventions that might benefit diabetic patients with CAN, and with attenuated ANS signaling to the SAN (58). In support of this contention, earlier studies have also shown that the kinetics of IKACh are regulated by RGS4 and PIP3 signaling in the SAN (83). RGS4 is inhibited by PIP3 which is activated by insulin-mediated phosphoinositide-3 kinase (PI3K) signaling. Therefore, impaired insulin and PI3K signaling in T2DM could result in enhanced RGS4 activity due to a loss of PIP3-mediated inhibition of RGS4 (84–86).
At the molecular level, the CaMKII pathway, known to maintain the pacemaker activity of SAN () is altered in diabetes and could lead to SAN anomalies. This is mainly achieved through the oxidation of CaMKII into ox-CaMKII which slows down the pacemaker activity of the SAN and promotes apoptosis of SANCs leading to high mortality in human and in experimentally diabetic animal models (, 87, 88). In fact, inhibition of CaMKII oxidation (mice lacking active NADPH oxidase), or pharmacological inhibition of CaMKII concedes resistance to apoptosis and fibrosis for injured SAN (87). Furthermore, using antioxidants in streptozotocin (STZ)-treated rats successfully reversed this process (87–89).
In addition to CaMKII sustained activity, hyperglycemia furthers the production of detrimental ROS that damage the cells and induce apoptosis leading to reduced SAN function. High blood glucose levels in diabetes increases diacylglycerol (DAG) content that activates protein kinase C (PKC). This in turn phosphorylates NADPH-oxidase, leading to further production of ROS. Such inflammatory reactions may also be associated with the action of advanced glycation end products (AGEs), which interact with their respective receptors (RAGE) on the cell surfaces, to produce the proinflammatory cytokines. Collectively, these promote inflammation, oxidative stress, and cellular death (90).
In SAN, basal PKC activity is crucial for normal spontaneous SANC activity. In freshly isolated rabbit SANCs, inhibition of PKC suppressed SR Ca2+ cycling and the spontaneous beating of the cells. Normally, SANCs firing is regulated by local subsarcolemmal Ca2+ release from the SR. Such release takes place during the SDD and stimulates NCX leading to an increased rate of SDD and acceleration of spontaneous SANC activity (91).
The pathological remodeling of the SAN in diabetic conditions resembles the one noticed in the elderly, whereby nodal cells are atrophied and are surrounded by infiltrated fibrous tissues (, ) (Figure 1). This profoundly alters the electrical conduction between the SANCs. In fact, the diabetes-induced fibrosis in STZ-treated rats detrimentally reduces the conduction properties of SAN tissues, often depicted by a wider P wave on the ECG tracings (92, 93). In contrast, the remodeling of the SAN in obese rats is manifested by hypertrophied SANCs and enlarged SAN tissues (94). Moreover, in diabetic conditions, the adenosine receptor AR1 is upregulated in the heart (95). Functional analysis showed that the upregulation of AR1 promotes SAN dysfunction and nodal conduction abnormalities (96). Thus, the direct effect of diabetes on SAN safety cannot be simply ignored. In addition, the indirect effect of diabetes on SAN tissues exemplified by the hypoperfusion of the SAN by the coronary arteries, due to their pathological remodeling in hyperglycemic conditions, profoundly alters SAN function.
Figure 1
4.3 Insights on Ion Channels Dysfunction and Cytoskeletal Remodeling in Diabetic SAN
Disruption of cardiac electrical activity has been widely observed in the hearts of both T1DM and T2DM patients (97). For example, prolongation of QRS and QT segments (98), disturbance in automaticity of SAN, atrioventricular block, and left bundle branch block have been commonly reported (99–101). T2DM patients have a high risk of atrial fibrillation (102, 103), ventricular arrhythmia (104), and fibrillation (105).
Similarly, prolonged QRS and QT intervals have also been reported in animal studies on diabetes. In isolated perfused hearts of non-obese Goto-Kakizaki (GK) T2DM rats, spontaneous HR was lower compared to control rats. This observation implies that the changes are, at least in part, due to an intrinsic abnormality in the cardiac electrical conduction system (106). Although earlier studies in animal models have reported a profound decrease in HR and increased mortality in diabetic animals (106), reports on SAN remodeling in diabetes are limited. In STZ-treated diabetic rats, HR was found to be slower compared to controls. Furthermore, SAN conduction and pacemaker cycle length and time were prolonged (107). Recently, in a recent, in leptin-receptor deficient T2DM diabetic mice, disturbance of systolic and diastolic activity of the heart, prolongation of SAN recovery time and relative autonomic denervation were reported (54).
Structural and/or functional channelopathies are thought to play a role in the electrical abnormalities reported in the diabetic heart. At the cellular level, diabetes reduces the velocity of SAN conduction and the slope of SDD and prolongs the duration of cardiac AP which is attributed to the altered expression and electrophysiological properties of various ion channels (97, 108–110) (Figure 2).
Figure 2
4.3.1 SAN Ion Channels
As mentioned earlier, the pacemaker activity of the SAN is regulated by several ion channels that are thought to contribute to the SDD. Specifically, the pacemaker activity is determined by a net inward current caused by the deactivation of outward current (IK,s) and the activation of inward currents, carried mainly by voltage-gated sodium channels (Nav1.5), hyperpolarization-activated cyclic nucleotide-gated channels (HCN), Cav3.1 channels and Cav1.3 channels (, , 111). Therefore, disruption of one or more of these ion channels would alter the electrophysiological properties of the SAN. Figure 3 shows the main ionic currents involved in the AP of SANCs.
Figure 3
4.3.1.1 Voltage Gated Sodium Channel (Nav1.5)
The voltage-gated sodium channel (Nav1.5) is predominantly expressed in the heart and governs the upstroke of the AP in the atrial and ventricular cells (112). However, its expression and distribution in the SAN tissues remain debatable. While studies showed the presence of the Nav1.5 in SAN tissues, others indicated that they are mainly expressed at the periphery but absent from the center of the SAN (113). Moreover, developmental studies showed that this particular isoform of the sodium channel is highly expressed at an early stage during development, and its expression is reduced later on when the heart adopts a slower rate of contraction (114). From the functional point of view, while studies showed an implication of Nav1.5 in the conduction of SANCs (115), others indicated that Nav1.5 rescues the pacing activity of SANs in hyperpolarization conditions (114).
In heterozygous knockout mice Nav1.5+/−, delayed conduction and arrhythmia were reported (116). In alloxan-induced diabetic rabbits, the protein level of Nav1.5 and the density of INa in the ventricle were significantly reduced (117). In agreement with this finding, Zhang et al. found that Nav1.5 was significantly decreased in the left atrium and right ventricle by 33% and 37%, respectively (118). However, Ferdous, et al. (2016) showed an upregulation of the gene encoding Nav1.5 in the SAN of STZ diabetic heart compared to normal (107). Such change in the expression of Nav1.5 could be an important determinant for arrhythmogenesis observed in diabetes. Furthermore, increased production of ROS in diabetic hearts, which is known to modify the properties of Na+ channels, could also contribute to the impaired SAN function in diabetes (119, 120).
4.3.1.2 Hyperpolarization-Activated Cyclic Nucleotide-Gated Channel
HCN channel conducts the hyperpolarization current (funny current; If). The channel activity is responsible for the spontaneous diastolic membrane depolarization of the SANCs and therefore the generation of spontaneous SAN AP. The channel is a tetramer that is composed of four HCN subunits that are made of six transmembrane segments. Although four HCN gene family members (HCN1, HCN2, HCN3 and HCN4) have been found in the heart, HCN4 is the prominent HCN in human SAN (121).
The HCN channel is modulated by cAMP (122). Specifically, the activity of the channel rises with the increase in intracellular concentrations of cAMP, which binds to the C-terminus of the channel (123). While cAMP activates the channel, muscarinic agonists inhibit the inward current at diastolic potentials by shifting the activation curve to more negative values (124). It is believed that regulation of HCN4 by cAMP in the heart is essential for HR modulation by the ANS. While cAMP-dependent increase in HCN4 activity is needed for the acceleration of the HR under ANS stimulation, a drop in the levels of cAMP following vagal stimulation lessens HCN4 activity and decreases HR (, 123).
Studies in animal models have reported that SANCs from knockout mice lacking HCN4 have a parallel decrease of 75% in If (125). In STZ T1DM, altered mRNA expression of HCN4 channels was reported (107). In support of this finding, a recent study conducted by Zhang et al. (2019) has shown a significant disturbance in the ECG characteristics of STZ-treated diabetic rats. This change was marked by prolongation of the PR interval, RR interval, QT interval and QRS complex. In addition, the beating rate of SAN was slower compared to control. Electrophysiological experiments showed that blocking of HCN4 channels with CsCl resulted in reduction of the beating rate of rat SAN preparations, indicating that HCN4 channels play a vital role in sustaining the spontaneous pacemaker activity. Along with the downregulation of HCN4 in the SAN, If was significantly reduced which could explain the observed reduction in SAN function (118).
Similarly, altered expression of HCN4 was reported in T2DM animals. In vivo experiments conducted in GK diabetic rats have shown that a decrease in the HR of young animals was coupled to downregulation of the expression of HCN4 gene (126). It is important to note that downregulation of HCN4 and If might be partly responsible for bradyarrhythmia observed in diabetic patients (127).
Although elevated ROS is a consistent finding in cardiovascular complications of diabetes, data on defined molecular targets and pathways that connect increased oxidation with SAN function are very limited. In sick sinus syndrome, mitochondrial oxidative stress was found to induce HCN4 downregulation (128). A recent study found that this effect involves the inhibition of mitochondrial thioredoxin-2, an important ROS scavenger that regulates the mitochondrial apoptosis signaling pathway. Indeed, the deletion of thioredoxin-2 in the whole mouse heart caused dilated cardiomyopathy, atrioventricular block and sinus bradycardia. The mice also displayed reduced expression of HCN4 in SANCs and typical electrophysiological signs of sick sinus syndrome (129).
4.3.1.3 T-Type Voltage-Gated Ca2+ Channel (Cav3.1)
The T-type voltage-gated Ca2+ channel plays a key role in cell excitation and Ca2+ handling in the heart. Three types of T-type Ca2+ channels were cloned; Cav3.1 (α1G), Cav3.2 (α1H) and Cav3.3 (α1I) (130). The Cav3.1 is highly expressed in the SAN and atrioventricular node, while it is poorly expressed in the myocardium. Cav3.1 contributes to the total Ca2+ current in the SAN. It was found to play a vital role in pace-making and impulse conduction in both mice and humans (131). The current generated by Cav3.1(ICa,T) is marked by delayed activation at voltages expanding over the diastolic depolarization phase, and rapid inactivation (132). It was reported that mice deficient in Cav3.1 had slower SAN recovery time, decelerated pacemaker activity of SAN and HR, and delayed atrioventricular conduction. These findings show that Cav3.1 is a major contributor to the generation of cardiac rhythmicity (132). An earlier study demonstrated that ICa,T of mouse SAN is activated by isoproterenol in a PKA-dependent manner; however, the physiological role of adrenergic control of ICa,Tis not well-understood (130).
Studies on the expression of Cav3.1 in diabetic animals reported conflicting results. Ferdous et al. (2016) have shown that in the SAN of STZ diabetic rats, mRNA expression of Cav3.1 is upregulated (107). In agreement with this finding, earlier studies have reported upregulation of Cav3.1 in the ventricle from the GK and the Zucker diabetic fatty rat (133, 134). It is expected that the upregulation of Cav3.1 upsurges T-type Ca2+ current and, consequently the slope of the pacemaker potential and HR in STZ rats. In contrast and in a more recent study, it has been shown that the expression of Cav3.1 gene is downregulated by three folds in GK rats. As a result, reductions in pacemaker activity and the slope of diastolic depolarization are expected (126, 132).
4.3.1.4 L-Type Voltage-Gated Ca2+ Channel (Cav1.3)
Two types of L-type voltage-gated Ca2+ channels, namely Cav1.2 and Cav1.3 are expressed in the heart; however, Cav1.3 is predominantly expressed in the SAN and atrioventricular node. In SAN, Cav1.3 not only contributes to the pacemaker activity but also to the initiation of diastolic depolarization and regulation of Ca2+ release from SR during SAN pacemaker activity (135, 136). Evidence shows that downregulation of the Cav1.3 gene in mice causes a reduction in pacemaker activity and causes spontaneous arrhythmia in SANCs (135).
Experiments in isolated perfused hearts of STZ diabetic animals have shown that decreased HR and prolonged SAN AP were associated with a significant decrease (32%) in the expression of Cav1.3 gene in diabetic SAN compared to control SAN (118). Previous studies have shown that deletion of the channel (Cav1.3–/–) caused the prolongation of the PR interval and the complete block of the atrioventricular conduction (137). As a result, downregulation of Cav1.3 could be a source of bradyarrhythmia and heart block in patients with T1DM. In GK diabetic rats, SAN Cav1.3 was also downregulated (126). This reduction in ICa,T observed in diabetes may be attributed to the change in the activation/inactivation kinetics of the channels, the expression of the channel proteins, or the change in the single-channel conductance. Although several studies have investigated the effect of diabetes on such electrophysiological properties in ventricular myocytes, the data on SAN Cav1.3 is scarce (138).
An earlier study examined the effect of CaMKII on SAN spontaneous excitation and modulation of ICa,L in freshly isolated rabbit single SANCs. It was found that inhibition of CaMKII can completely arrest SANCs largely as a result of depressed ICa, L amplitude, reduced window current, and slowed recovery of L-type Ca2+ channels from inactivation. This finding shows a key role of CaMKII in regulating cardiac pacemaker activity ().
4.3.2 SAN Cytoskeletal Proteins
Cytoskeleton proteins support cell shape, elasticity, and contractility. For example, collagen I is an extracellular protein that provides a structural framework to the cardiac myocytes, stiffness to the myocardial wall, and assists in force transmission (139). Therefore, changes in the level of expression of this protein affects the conduction properties in the heart, thus promoting arrhythmogenesis. In fact, several studies have shown that collagen I is overexpressed in diabetic rat hearts, which would contribute to the decreased ventricular compliance (140). A recent study in STZ diabetic rats has shown an increase in the level of collagen I expression throughout the conduction system in the heart including the SAN (118).
Caveolin-3 is a structural and regulatory protein that modulates the function of ion channels, including those involved in pace-making (141). Mutations in the gene encoding caveolin-3 have been linked to several cardiac diseases such as long QT syndrome, myocardial hypertrophy, and diabetic cardiomyopathy (142, 143). SAN cells are rich in caveolin-3 protein (144). Studies have shown that caveolin-3 co-localizes with HCN4 channel and affects its function (145). The expression of caveolin-3 mutant modifies the gating properties of HCN4 channels by causing a rightward shift in the activation curve (146). Furthermore, when caveolae are disturbed in the SAN, β2-adrenergic receptor regulation of HCN4 channel was found to be lost (145). In spontaneously beating neonatal cardiac cells, the T78M mutation of the caveolin-3 gene significantly enhanced peak-to-peak AP variability linked to rightward shift of activation potential of HCN4 channels (147). In support of the vital role of Caveolin-3 in SAN function, Lang et al. (2016) found that in caveolin-3 knockout mice, heart rate fluctuation with altering periods of bradycardia-tachycardia rhythm was observed. Such change was linked to the disturbance of SAN function (144). In chronic STZ-induced diabetic rats, lower expression of caveolin-3 was detected (148, 149).
PKC-β2 is known to be overexpressed in the diabetic heart and contributes to cardiomyocyte hypertrophy in diabetes. Interestingly, impairment in caveolin-3 expression was found to be one of the underlying mechanisms for cardiac dysfunction that is linked to hyperglycemia-induced PKC-β2 activation (150). Therefore, it is expected that changes in the expression of caveolin-3 in any region in the heart may contribute to the pathogenesis of diabetic cardiomyopathy. However, data on the altered expression of caveolin-3 in the SAN of diabetic rats is scarce. In addition, α-actinin is another structural protein involved in maintaining cell shape and contractility. A significant decrease in the expression of α-actinin was observed throughout the heart regions but not in the diabetic SAN (118).
A hallmark of cell-to-cell coupling is the gap junction at the intercalated discs, forming macrochannels for effective transmission and propagation of the AP between cardiac cells. The expression and distribution of the different variants of connexins-Cx (the proteins forming gap junctions) is specific to each different area of the SAN (151). While Cx40, Cx45, and Cx46 are abundantly distributed in the central area of the SAN, Cx43 is almost non-existent in this tissue (). The heterogeneity of the expression of these Gap junction proteins explains the distinctiveness of conduction through the SAN. Of interest, one of the striking remodeling features in diabetic cardiomyopathy is the persistently reduced transmission of the AP through gap junctions. In fact, the function of Cx43, which is predominantly expressed in the working myocardium, depends on tyrosine phosphorylation. Both the expression/distribution and phosphorylation of Cx43 are altered in diabetic hearts, leading to reduced impulse propagation which increases the risk for the development of fibrillation (152, 153). In SAN from diabetic animal models, the expression of Cx40, Cx43, and Cx45 is still controversial. Howarth et al. (2007) showed a moderate increase of these connexins in the SAN of the STZ-treated rats (154). However, Ferdous et al. (2016) reported an increase in the mRNA of Cx45 in the SAN of STZ-treated rats, without a significant change in the expression pattern of the Cx40 and Cx43 (107). The literature falls short on the implication of Cx40 and Cx45 in the electrical remodeling of the diabetic SAN, the slow conductance of the AP, and consequently cardiac rhythm. This warrants extensive investigation to fill this gap in the literature and to help stabilize cardiac rhythm in diabetic conditions.
4.4 Electrophysiological Effects of Anti-Diabetic Drugs on SAN Currents
While few studies indicate that anti-diabetic drugs significantly protect the cardiovascular system, other controversial reports conclude that anti-diabetic medicine is far from reversing the cardiac complications manifested in diabetic settings (155). For example, Metformin, a medicine used to treat T2DM, stimulates the 5′ adenosine monophosphate-activated protein kinase (AMPK) signaling pathway, which consequently stimulates the ATP-sensitive potassium channels (KATP) involved in the control of HR (156). In the same vein, the activation of AMPK contributes to the maintenance of the ICa,L, the ICa,L- triggered Ca2+ transients amplitude, the Ca2+ content, and promotes cell contraction (157).
Rosiglitazone, the thiazolidinedione class of anti-diabetic drugs, acts to inhibit KATP channels in the pancreatic β-cells (158). Inhibition of these channels by high levels of ATP causes membrane depolarization, Ca2+ influx through voltage-gated Ca2+ channels and Ca2+ -dependent secretion of insulin; thus inhibition of pancreatic KATP channels prevents insulin secretion (159). Conversely, the blockade of the cardiac isoform of the KATP channel (KIR6.2/SUR2A) severely compromises the cardiac ability to cope with ischemic assaults (158, 160–162), implying that the KATP of SANCs would be tremendously altered in diabetic patients on Rosiglitazone treatment. However, existing studies do not provide confirmatory information on the role of anti-diabetic drugs on the AP of SANCs. This field warrants further investigations.
While insulin remains an ultimate treatment for a large group of diabetic patients, its effect on the electrophysiological properties of cardiac cells remains inexplicit. However, few studies highlighted an implication of insulin in the electrical activity of cardiac myocytes. For example, in myocytes isolated from T1DM diabetic hearts, the main affected repolarizing current is the Ito (138). In an earlier report (1999), Shimoni and colleagues have shown that insulin treatment of isolated ventricular myocytes from STZ diabetic rats reverses the depression of ventricular K+ currents (163). Moreover, insulin mediates its effect through insulin receptors and the cAMP-dependent PKA to stimulate ICa,L in isolated rat ventricular myocytes in a dose-dependent and reversible manner (164). Interestingly, insulin may also play a role in both the “M” and “Ca2+” clock systems by stimulating Ca2+-ATPase activity at the SR and the SL, and by increasing the Na+/Ca2+ exchange activity (164).
It is noticed that in insulin-resistant cardiac tissues, the normal rise in a calcium-independent sustained K+ current is either reduced or eradicated (165). The addition of insulin to myocytes isolated from insulin-resistant rats, treated with metformin (an insulin-sensitizing drug), produced a very significant enhancement of sustained K+ current (165). Thus, Metformin modulates the insulin resistance effect observed for cardiac K+ current which implies that these changes may also occur at the SAN level. In addition, both acute and chronic insulin treatment improved sodium currents in the atrial muscle of T1DM Atika mice by promoting the electrical properties of the Nav1.5 channel and by increasing its expression. This stabilization effect of insulin on atrial fibrillation could probably be stretched on SAN tissues since they express the Nav1.5 channel, and since arrhythmic SANCs are a hallmark of diabetes in animal models (54, 166).
5 Conclusion and Future Perspectives
Despite its primordial role in generating the AP waves that drive cardiac contractions, the dynamics of the SAN in diabetic settings remain ill-defined. It is clear that hyperglycemia modulates the expression/function of the ion channels underlying the electrical properties of the SANCs. This is manifested by repression of the currents involved in the upstroke of the AP and the conduction of SAN tissues. Chronic anti-diabetes treatments (metformin, insulin, rosiglitazone) adversely affect the SAN and, consequently, cardiac function. This is in addition to the structural/functional changes that underscore diabetic cardiomyopathy (working myocardium and other parts of the conduction system, i.e., the atrioventricular node and Purkinje fibers). Although various animal models are now established to study diabetes, the literature falls short on the synergy of the SAN during this metabolic syndrome. This includes a gap in the knowledge on the structural remodeling of SAN in diabetes as well as the metabolic changes induced by diabetes in the SANC. This calls for more investigations focused on the molecular signature of diabetes-induced SAN dysfunction to build an informative platform that links the clinical aspect of SAN failure with diabetes, and to provide a safer therapeutic approach for this metabolic disorder of the cardiac pacemaker. The advent of live imaging and optical mapping provides unique tools to study the metabolic and electrical changes in human diabetic SANCs. An alternative and more attractive approach would be a targeted therapy (pharmacological or genetic) of the SAN in diabetic subjects to warrant normal pacemaker activity and typical cardiac function. The different modalities of diabetic SAN injuries showcased herein must be carefully considered in the field of biological SAN engineering to develop a diabetes-resistant SAN for patients with diabetes.
Publisher’s Note
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Author contributions
LTA and MN: Conceptualization of the manuscript. LTA, SC, EA, AAK, MN: Writing the original manuscript and editing. All authors contributed to the article and approved the submitted version.
Conflict of interest
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.
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Summary
Keywords
sinoatrial node, diabetes, action potential, ion channels, gap junctions, structural remodeling, metabolic changes
Citation
Al Kury LT, Chacar S, Alefishat E, Khraibi AA and Nader M (2022) Structural and Electrical Remodeling of the Sinoatrial Node in Diabetes: New Dimensions and Perspectives. Front. Endocrinol. 13:946313. doi: 10.3389/fendo.2022.946313
Received
17 May 2022
Accepted
14 June 2022
Published
07 July 2022
Volume
13 - 2022
Edited by
Lu Cai, University of Louisville, United States
Reviewed by
Di Lang, University of Wisconsin-Madison, United States; Henggui Zhang, The University of Manchester, United Kingdom
Updates
Copyright
© 2022 Al Kury, Chacar, Alefishat, Khraibi and Nader.
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.
*Correspondence: Lina T. Al Kury, Lina.AlKury@zu.ac.ae; Moni Nader, moni.nader@ku.ac.ae
†These authors have contributed equally to this work
This article was submitted to Cardiovascular Endocrinology, a section of the journal Frontiers in Endocrinology
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