The Pattern of mRNA Expression Is Changed in Sinoatrial Node from Goto-Kakizaki Type 2 Diabetic Rat Heart.
Cardiovascular complications are widely reported in diabetic patients and may be associated with various cardiac arrhythmias and sudden cardiac death [1-5]. Although coronary artery disease and hypertension are risk factors for cardiovascular dysfunction in diabetic patients, there is also a risk of developing cardiac dysfunction that is independent of coronary atherosclerosis and hypertension . Electrical disturbances have been widely reported in diabetic heart [7, 8]. Bolognesi et al.  reported that sinus bradycardia and QT prolongation can occur in insulin-treated diabetic patients with severe hypoglycemia. Abnormal functions of sinus node automaticity, third-degree atrioventricular block, and left bundle branch block occur more frequently in diabetic patients [10-12]. Type 2 diabetic patients have an increased risk of supraventricular arrhythmias including atrial fibrillation [1, 13-16], ventricular tachyarrhythmias, and ventricular fibrillation [3, 5, 7, 17]. Various studies have shown that QT prolongation is an independent risk factor for cardiovascular mortality in diabetic patients [2, 18-21]. Howarth et al.  reported disturbances in the electrocardiogram including bradycardia and prolongation of the QRS and QT intervals in the GK rat. Soltysinska et al.  reported alterations in systolic and diastolic function and prolonged SAN recovery time in db/db diabetic mice. Hyperglycemia, a hallmark of diabetes mellitus, is associated with oxidative stress which in turn exacerbates inflammation and further exacerbates oxidative stress, which in turn may partly underlie QT prolongation and trigger ventricular arrhythmias [24, 25].
In the Zucker diabetic fatty rat, myocardial impulse propagation was impaired . Little is known about the effects of type 2 diabetes mellitus (T2DM) on the electrophysiology of the SAN. In the streptozotocin- (STZ-) induced diabetic rat, SAN conduction, pacemaker cycle length, and action potential duration were prolonged [27, 28]. Various ion channels and ionic conductances including L-type and T-type [Ca.sup.2+] current, hyperpolarization-activated "funny" current, [Na.sup.+] current, [Na.sup.+]/[Ca.sup.2+] exchange current, and various [K.sup.+] currents are essential for the generation, propagation, and regulation of the SAN action potential . Sarcoplasmic reticulum (SR) [Ca.sup.2+] might also contribute to the generation and decay of the SAN action potential . Structural and/or functional channelopathies may underlie some of the electrical abnormalities that have been reported in diabetic heart . In order to further elucidate the molecular basis of these heart rhythm disturbances, we have investigated the pattern of more than 70 genes encoding proteins that are associated with the generation and conduction of electrical activity in the SAN in the GK type 2 diabetic heart. Results from this study will provide direction for future structural and functional studies of the electrical conduction system in the diabetic SAN.
2. Materials and Methods
2.1. Experimental Protocol. Ethical approval for this project was obtained from the Animal Ethics Committee, College of Medicine & Health Sciences, UAE University. Male GK and Wistar control rats were reared as previously described . Rats were kept in cages, under a 12 h-12 h light-dark cycle, and had free access to food and tap water. Room temperature was kept between 21 and 25[degrees]C. Experiments commenced when the animals were 12-13 months of age. Blood glucose, after an overnight fast, and blood glucose 120 min after a glucose challenge (2 g/kg body weight, intraperitoneal) were measured in GK and age-matched controls. Prior to experiments, the body weight, heart weight, and the nonfasting blood glucose were also measured. The heart to body weight ratio was calculated.
2.2. Measurement of Heart Rate. Rats were sacrificed as previously described using a guillotine . The chest was then opened, and the hearts were rapidly removed and mounted in Langendorff mode and perfused at a constant flow rate of 8 ml.g [heart.sup.-1] [min.sup.-1] at 36-37[degrees]C with normal Tyrode containing 140 mM NaCl, 5 mM KCl, 1 mM Mg[Cl.sub.2], 10 mM glucose, 5 mM HEPES, and 1.8 mM Ca[Cl.sub.2] and adjusted to pH7.4 with NaOH bubbled with oxygen. An extracellular suction electrode was used to measure heart rate according to previously described techniques . Action potentials were recorded in the left ventricle. Electrical signals were collected at 400 Hz. Signals were then amplified (ADInstuments, ML136 Bioamp), delivered to a Powerlab (ADInstruments, PL410), and displayed on a PC monitor. Analysis was performed using ADInstruments software version v 4.21 (ADInstruments, Australia).
2.3. Expression of mRNA. Previously described techniques were used to evaluate the expression of genes encoding more than 70 proteins involved in electrical activity in the SAN [32, 34-36]. After rats were sacrificed, the hearts were rapidly removed and placed in a plastic dish containing NaCl 140 mM, KCl 5.4 mM, Mg[Cl.sub.2] 1 mM, HEPES 5 mM, D-glucose 5.5 mM, and Ca[Cl.sub.2] 1.8 mM and adjusted to pH7.4 with NaOH. The ventricles and the left atrium were removed, and the right atrium was opened to expose the SAN and crista terminalis. The SAN artery was used to identify the SAN. The SAN was exposed, and 2 mm biopsy samples of SAN were carefully collected from GK and control rat hearts according to previously described techniques . The samples were placed in RNA later (AM7021, Life Technologies, Carlsbad, CA, USA) and stored overnight at room temperature to allow thorough penetration of the tissue . The following day, tissue samples were frozen at -20[degrees]C in readiness for further processing. Tissue samples were homogenized in homogenization microtubes containing 1.4 mm ceramic beads using a Precellys 24 tissue homogenizer (Bertin Technologies, USA). The homogenization protocol comprised 2 runs at 6500 rpm of 20 seconds each with a 15-second gap. The SV Total RNA Isolation System (Promega, Madison, USA) was used to isolate total RNA from the tissue, in accordance with the manufacturer's instructions. Spectrophotometric techniques were used to measure the concentration and purity of the RNA samples. The absorbance was measured at 260 nm, and the ratio of absorbance was measured at 260 nm and 280nm (ND-1000, NanoDrop). cDNA was generated using a 2-step RT-PCR procedure. Total RNA (500 ng) was converted into cDNA in a 25 [micro]l PCR reaction with 10x RT Buffer 2.0 [micro]l, 25x dNTP Mix (100mM) 0.8 [micro]l, 10x RT Random Primers 2.0 [micro]l, MultiScribe[TM] Reverse Transcriptase 1.0 [micro]l, RNase inhibitor 1.0 [micro]l, and Nuclease-free H2O (High Capacity cDNA Reverse Transcription Kit, 4374966, Applied Biosystems, USA). A Veriti thermal cycler (Applied Biosystems, USA) was used to perform reverse transcription. The cycles were as follows: 10 min at 5[degrees]C, 120 min at 37[degrees]C, and 5 min at 85[degrees]C. Customized TaqMan Low Density Arrays (Format 32, 4346799, Applied Biosystems, USA) were used for gene expression assays. The TaqMan assays were preloaded in triplicate for each RNA sample. Rat glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was selected as the endogenous control [35, 37]. The expression of GAPDH was not significantly different (p > 0.05) between GK and control SAN samples. 100 ng of cDNA was loaded, together with 2x TaqMan Gene Expression Master Mix (No AmpErase UNG, Applied Biosystems, USA), for a total of 100 [micro]l per port. Two SAN tissue samples were combined for each real-time RT-PCR assay. Real-time RT-PCR was carried out in a Fast ABI Prism 7900HT Sequence Detection System (Applied Biosystems, USA). Standard mode PCR thermal cycling parameters were run as follows: 2 min at 50[degrees]C, 10 min at 94.5[degrees]C, and 40 cycles of 30 sec at 97[degrees]C and 59.7[degrees]C for 1 min. Analysis was performed using ABI Prism 7900HT SDS, v2.4 software. Statistical analysis was performed using SDS RQ Manager 1.1.4 software employing the [2.sup.-[DELTA][DELTA]Ct] method with a relative quantification RQmin/RQmax confidence set at 95%. The lists of target genes, encoded proteins, and description of the proteins are shown in Table 1.
2.4. Statistics. Data were expressed as the mean [+ or -] SEM of "n" observations. Statistical comparisons were performed using an independent samples t-test (SPSS v. 20), and a "p" value of less than 0.5 was considered to indicate a significant difference.
3.1. General Characteristics. Nonfasting blood glucose and fasting blood glucose were significantly (p < 0.01) elevated in GK rats compared to age-matched controls. After an overnight fast blood glucose, 120 min following a glucose challenge (2 g/kg body weight, intraperitoneal), was also significantly (p < 0.01) elevated in GK compared to controls. Body weight and heart weight were significantly (p < 0.01) increased, and heart weight/body weight ratio was significantly (p < 0.05) reduced in GK compared to controls (Table 2).
3.2. Heart Rate. Heart rate is shown in Figure 1. Heart rate was significantly (p < 0.01) reduced in GK (161 [+ or -] 12 bpm, n = 10) compared to control (229 [+ or -] 11 bpm, n = 10) heart (Figure 1).
3.3. Expression of mRNA. Figure 2 shows the expression of mRNA for gap junction proteins. Expression of Gja1 (2-fold), Gja5 (4-fold), Gjc1, and Gjd3 (4-fold) were all downregulated in GK compared to control SAN. Figures 3(a) and 3(b) show expression of mRNA for cell membrane transport and intracellular [Ca.sup.2+] transport and regulatory proteins, respectively. Expression of Trpc1 and Trpc6 (6-fold) and Itpr1-3 (2-fold) were downregulated, and Ryr2 was upregulated in GK compared to control SAN. Figure 4 shows the expression of mRNA for hyperpolarization-activated cyclic nucleotide-gated channel proteins. Expression of Hcn1 (4-fold) and Hcn4 (5-fold) were downregulated in GK compared to control SAN. Figure 5 shows the expression of mRNA for calcium channel proteins. Expression of Cacna1d (3-fold), Cacna1g, Cacna1h (4-fold), Cacna2d1, Cacna2d3, and Cacng4 (3-fold) were downregulated in GK compared to control SAN. Figures 6(a) and 6(b) show the expression of mRNA for potassium channel proteins. Expression of Kcna2, Kcna4, Kcna5 (5-fold), Kcnb1, Kcnd3, Kcnj2, Kcnk1 (7-fold), Kcnk5 (3-fold), Kcnk6, and Kcnn2 were downregulated, and Kcnj11, Kcnj5, and Kcnk2 were upregulated in GK compared to control SAN. Figure 7 shows the expression of mRNA for various other proteins that might affect electrical activity in the SAN. Expression of Abcc9 and Nppb were upregulated in GK compared to control SAN.
Previous in vivo biotelemetry experiments performed in GK type 2 diabetic rats have demonstrated disturbances in the electrocardiogram. These disturbances have included reduced heart rate which was associated with prolonged QRS and QT intervals . The spontaneous heart beat in isolated perfused heart was also lower in GK compared to control rats which suggests that the bradycardia is at least partly attributed to an intrinsic defect in the electrical conduction system of the heart . Changes in membrane potential that occur during the different phases of the SAN action potential are produced by changes in the movement of various ions ([Na.sup.+], [Ca.sup.2+], and [K.sup.+]) across the cell membrane and by the movement of [Ca.sup.2+] in or out of the SR .
Disturbances in one or more of these ionic conductances would be expected to alter the electrophysiological properties of the SAN. In order to further clarify the molecular basis of the low heart rate in the GK rat, the expression of more than 70 genes that encode proteins that are associated with the generation and conduction of electrical activity in the GK SAN were evaluated.
Regarding the changes in mRNA of particular interest were (i) downregulation of Gja5 and Gjd3 (4-fold), (ii) downregulation of Trpc6 (6-fold), (iii) downregulation of Hcn4 (5-fold), (iv) downregulation of Cacna1d (3-fold), Cacna1h (4-fold), and Cacng4 (3-fold), (v) downregulation of Kcna5 (5-fold) and Kcnk1 (7-fold) in GK compared to control SAN, and (vi) upregulation of Nppb in GK compared to control SAN.
Gja5 (Cx40) and Gjd3 (Cx31.9) were downregulated in GK compared to control SAN. The connexins are structurally related proteins that assemble to form gap junctions which play an important role in cell-to-cell electrical communication and cardiac rhythmicity. At least 5 connexins (Connexin30.2, Connexin37, Connexin40, Connexin43, and Connexin45) are expressed in the heart, and each connexin displays regional and cell type-specific expression . Downregulation of connexin proteins may result in impaired electrical conduction between cells and, hence, may have implications for electrical transmission among the cells of the SAN and between the SAN and other regions of the heart .
Trpc6 (TRPC6) and to a lesser extent Trpc1 (TRPC1) were downregulated in GK compared to control SAN. The transient receptor potential channels (TRPCs) are a large family of ion channels that are widely expressed in human tissue including the heart and the vasculature [39, 40]. TRPC1 and TRPC6 are stretch-activated, nonselective cation channels expressed in ventricular muscle from mouse heart . The TRPCs have been found to play a role in cardiovascular disease . Upregulation of TRPCs is involved in the pathophysiology of cardiac hypertrophy and heart failure [39, 43, 44]. Previous studies have demonstrated that cardiac hypertrophy upregulated TRPC6 and inhibition of TRPC6 suppressed agonist-induced hypertrophic responses [45-47]. Downregulation of Trpc1 and Trpc6 in the GK SAN may have implications for the conduction of [Na.sup.+] or [Ca.sup.2+] current through nonselective TRPCs and in turn implications for the generation of action potentials in SAN cells [43, 48, 49].
The SAN generates action potentials automatically, and the cells of the SAN appear to have two separate but closely communicating mechanisms (often referred to as "clocks"). There is a "membrane clock" which consists of ion channels that include the hyperpolarization-activated cyclic nucleotide-gated channels (mainly HCN4), the L-type [Ca.sup.2+] channels (mainly [Ca.sub.v]1.3), and the T-type [Ca.sup.2+] channels (mainly [Ca.sub.v]3.1). There is also a "calcium clock" which consists of [Ca.sup.2+]-handling proteins that include the ryanodine receptor (RyR2), the sarcoplasmic reticulum-ATPase (SERCA2a), and the [Na.sup.+]/[Ca.sup.2+] exchanger (NCX1) [50, 51]. Recent studies in human nodal cells have shown that when the clocks become uncoupled, SAN cells fail to generate spontaneous action potentials and [beta]-adrenergic receptor stimulation, which in turn increases cyclic AMP concentration and was able to restore spontaneous, rhythmic action potentials . HCN1-4 proteins are the structural components of the funny channels, and the funny current (If) is the main electrical driving force behind diastolic depolarization.
Hcn4 (HCN4) and to a lesser extent Hcn1 (HCN1) were downregulated in GK compared to control SAN. Shinagawa et al.  have shown that a variety of time-dependent and voltage-dependent ionic currents contribute to the rat action potential including the delayed rectifier [K.sup.+] current, the L-type [Ca.sup.2+] current, and [Na.sup.+] current. Hcn4 and Hcn1 are variously expressed in rat atrioventricular node, SAN, right atrium, and ventricle . In human, SAN Hcn4 accounts for 75%, Hcn1 for 21%, Hcn2 for 3%, and Hcn3 for 0.7% of the Hcn in human SAN . It has been shown that Hcn4-related inheritable arrhythmias, resulting in four different mutations of the Hcn4 gene, are associated with reduced heart rate and various arrhythmias . Hcn1 (HCN1) was reduced in GK compared to control SAN. In the absence of the pacemaker channel protein HCN1, mice display congenital SAN dysfunction that was characterized by low heart rate, sinus arrhythmia, increased SAN conduction and recovery time, and recurrent sinus pauses . Downregulation of Hcn1 and Hcn4 might be expected to reduce the slope of the pacemaker potential, prolong the time to threshold potential, and partly underlie the bradycardia in the GK rat heart.
Cacna1d ([Ca.sub.v]1.3), Cacna1h (Cav3.2), and Cacng4 ([Cav.sub.[gamma]]4) were downregulated in GK compared to control SAN. Voltage-gated L-type and T-type [Ca.sup.2+] channels are found in the heart. L-type and T-type [Ca.sup.2+] currents are important in the generation of phase 4, and L-type [Ca.sup.2+] current is also important in the generation of phase 0 of SAN and atrioventricular node action potentials. The T-type [Ca.sup.2+] channels also have roles in cell growth and cardiovascular remodeling. Cacna1g ([Ca.sub.v]3.1) and Cacna 1h ([Ca.sub.v]3.2) encode pore-forming alpha(1) subunits of the T-type [Ca.sup.2+] channel in cardiac muscle . Cacna1g ([Ca.sub.v]3.1) and Cacna1h (Cav3.2) may be involved in the development of the heart's electrical conduction system . In adult heart, the T-type [Ca.sup.2+] channel is widely distributed in the conduction system and plays an important role in the generation of the pacemaker depolarization in phase 4 of the SAN action potential . Downregulation of Cacna1h (Cav3.2) might have consequences for the generation of the pacemaker potential and, therefore, the heart rate in the GK SAN. Interestingly, Cacna1c ([Ca.sub.v]1.2) which mediates the generation of the pacemaker potential and action potential in the SAN was also modestly reduced in GK compared to control SAN. The gamma subunits of the L-type [Ca.sup.2+] channel, of which there are 8 isoforms, differentially modulate [Ca.sup.2+] channel function . Reductions in expression of Cacna1d ([Ca.sub.v]1.3) and Cacng4 ([Cav.sub.[gamma]]4) would be consistent with depressed L-type [Ca.sup.2+] current and modulation of the L-type [Ca.sup.2+] channel activity and have implications for the pacemaker potential and generation of the action potential and, hence, heart rate in the GK rat heart.
Compared to controls, the general characteristics of the GK rat included elevated nonfasting and fasting blood glucose and glucose intolerance, as evidenced by the raised blood glucose 120 min following a glucose challenge, after an overnight fast. RyR2 channels are found in sarcoplasmic reticulum and have important roles in cardiac myocyte contraction and the generation of autorhythmicity in SAN cells . Recent studies have revealed a crucial role of RyR2 channels in the regulation of insulin release and glucose homeostasis . RyR2 was upregulated in GK compared to CON SAN, and it would be interesting to investigate if the expression of pancreatic [beta]-cell RyR2 is also altered in GK rat which in turn might partly underlie the hyperinsulinemia previously reported in GK compared to CON rat .
Kcna5 ([K.sub.v]1.5) and Kcnk1 (TWIK1) were downregulated in GK compared to control SAN. Kcna5 (Kv1.5) encodes the potassium channel [alpha]-subunit [K.sub.v]1.5 and is widely expressed in heart, brain, and vascular, airway, and smooth muscle cells [62-64]. Within the heart, several studies have demonstrated the presence of [K.sub.v]1.5 in atria, ventricle, and SAN [65-67]. The cardiac ultrarapid outward ([I.sub.Kur]) current, which is encoded by Kcna5, controls action potential duration and in particular repolarizing current [68-70]. Remodeling of ion channels, including the voltage-gated potassium channel [K.sub.v]1.5, is involved in the pathophysiology of atrial fibrillation . Expression of [K.sub.v]1.5 results in marked decreases in mouse ventricular myocyte action potential duration . In vivo overexpression of [K.sub.v]1.5 has been shown to shorten action potential duration, eliminate after depolarizations, and increase heart rate in mice with long QT syndrome . Downregulation of Kcna5 might result in prolonged repolarization and duration of the action potential and, as a consequence, reduction in heart rate.
Kcnk1 (TWIK1) is widely expressed in the human heart and brain . TWIK1 channels may be involved in the regulation of the resting membrane potential and, hence, excitability of the cardiac myocyte [75, 76]. Downregulation of Kcnk1 might have implications for resting membrane potential and, hence, excitability of the SAN cell. Abnormal QT prolongation is not an uncommon feature in diabetic heart, and this is associated with reduction in the rapid delayed rectifier [K.sup.+] current (IKr) in insulin-dependent diabetic heart . Kcnh2, the gene that encodes expression of KCNH2 protein (also known as hERG1) that encodes the hERG channel, was not significantly altered in diabetic SAN.
Nppb (BNP) and to a lesser extent Nppa (ANP) were upregulated in GK compared to control SAN. BNP and ANP are secreted by the atria and ventricles and cause a reduction in blood pressure and cardiac hypertrophy. In the heart, BNP reduces ventricular fibrosis, and BNP and ANP are involved in the pathophysiology of heart failure, coronary heart disease, hypertension, and left ventricular hypertrophy [78-80]. Increases in BNP and ANP in blood plasma and atrial tissues are associated with varying effects of these natriuretic peptides on the amplitude and kinetics of shortening and intracellular [Ca.sup.2+] in ventricular myocytes from STZ-induced diabetic rat [81, 82]. Springer et al.  reported that BNP increased electrical conduction velocity and heart rate in isolated heart and in the SAN and also increased spontaneous action potential frequency in SAN cells. Upregulation of Nppb (BNP) and Nppa (ANP) may be associated with mechanisms that compensate for low heart rate in the GK type 2 diabetic rat heart.
It is of interest to compare gene expression in the current study with that in a recent study in SAN from the STZ-induced diabetic rat . For example, Gja5 (Cx40) and Gjd3 (Cx31.9) were downregulated in GK and unaltered in STZ SAN; Trpc6 (TRPC6) was downregulated in GK and upregulated in STZ SAN; Ryr2 (RYR2) was upregulated in GK and unaltered in STZ SAN; Hcn1 (HCN1) and Hcn4 (HCN4) were downregulated in GK and unaltered in STZ SAN; Cacna1d ([Ca.sub.v]1.3), Cacna1h (Cav3.2), and Cacng4 ([Cav.sub.[gamma]]4) were downregulated in GK SAN; however, in the STZ study, Cacna1d was unaltered, Cacna1h was upregulated, and Cacng4 was downregulated; Kcna5 ([K.sub.v]1.5) and Kcnk1 (TWIK1) were downregulated in GK SAN and unaltered in STZ SAN; Nppb (BNP) was upregulated in GK and in STZ SAN. These differences may be partly attributable to the different ages of the animals (GK/CON rats 12-13 months vs. STZ/CON rats 18 weeks of age) and the nature of diabetes (GK genetic vs. STZ chemical induced) in the two experimental models.
Heart failure and T2DM are two increasingly common and related diseases. MicroRNAs (miRs) play an important role in the pathogenesis of structural alterations in the failing heart . Some patients, who are affected by heart failure and who have severe hemodynamic and electrical dysfunction, receive cardiac resynchronization therapy (CRT). Recent studies have shown that CRT is associated with alterations in expression of genes and miRs which regulate a variety of cardiac processes including cardiac apoptosis, cardiac fibrosis, cardiac hypertrophy, cardiac angiogenesis, and membrane channel ionic currents [85, 86]. In the future, interventions that are able to alter expression of miRs might become an important treatment modality for diabetes and heart failure.
The molecular biology results are based on quantitative PCR. The possibility of posttranscriptional modifications, for example, by miR, means that changes in gene expression might not necessarily result in corresponding changes in the expression of proteins. Previous studies have demonstrated that spironolactone regulates HCN protein expression through miR-1 in rats with myocardial infarction and interestingly, upregulation of miR-1 expression partially contributed to the posttranscriptional repression of HCN protein expression . Recent studies have demonstrated that multiple miRs are involved in the regulation of SCN5A/ Nav1.5 channel and its [beta]1/SCN1B subunit which is responsible for the fast-activating, fast-inactivating sodium current in atrial and ventricular action potentials . Further structural experiments will be required to investigate the expression of selected proteins and the consequences of these structural changes on the electrophysiology of ion channels in the diabetic heart.
It is hoped that results emerging from laboratory studies will eventually translate into treatment modalities, which might include manipulation of miRs, mRNAs, and associated conduction proteins, in order to normalize electrical dysfunction in the diabetic heart.
In conclusion, this study provides valuable insight into the differences in expression of genes that encode proteins that are involved in the generation and conduction of electrical activity in the SAN in the GK diabetic rat and will form the basis for future structural and electrophysiological studies.
The raw mRNA data and statistically analyzed data presented in the figures are available, should it be requested, or available from the corresponding author upon request.
Conflicts of Interest
The authors declare no competing financial or nonfinancial interests.
The authors received a research grant from the UAE University.
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F. C. Howarth [ID], (1) M. A. Qureshi, (1) P. Jayaprakash, (2) K. Parekh, (1) M. Oz, (2) H. Dobrzynski, (3) and T. E. Adrian (4)
(1) Department of Physiology, College of Medicine & Health Sciences, UAE University, Al Ain, UAE
(2) Department of Pharmacology, College of Medicine & Health Sciences, UAE University, Al Ain, UAE
(3) Cardiovascular Sciences, University of Manchester, Manchester, UK
(4) Department of Basic Medical Sciences, Mohammed Bin Rashid University of Medicine & Health Sciences, Dubai, UAE
Correspondence should be addressed to F. C. Howarth; email@example.com
Received 10 June 2018; Revised 16 July 2018; Accepted 12 August 2018; Published 2 September 2018
Academic Editor: Michaelangela Barbieri
Caption: Figure 1: Heart rates in GK and control rats. Data are mean [+ or -] SEM, n = 10 hearts.
Caption: Figure 2: Expression of genes encoding various gap junction proteins. Data are mean [+ or -] SEM, n = 9 samples, each containing SANs from 2 hearts.
Caption: Figure 3: (a) Expression of genes encoding various membrane transport and (b) intracellular [Ca.sup.2+] transport and regulatory proteins. Data are mean [+ or -] SEM, n=6-9 samples, each containing SANs from 2 hearts.
Caption: Figure 4: Expression of genes encoding various hyperpolarization-activated cyclic nucleotide-gated channels. Data are mean [+ or -] SEM, n=6-8 samples, each containing SANs from 2 hearts.
Caption: Figure 5: Expression of genes encoding various calcium channel proteins. Data are mean [+ or -] SEM, n=7-9 samples, each containing SANs from 2 hearts.
Caption: Figure 6: (a) and (b) Expression of genes encoding various potassium channel proteins. Data are mean [+ or -] SEM, n=8-9 samples, each containing SANs from 2 hearts.
Caption: Figure 7: Expression of genes encoding miscellaneous cardiac proteins. Data are mean [+ or -] SEM, n=5-9 samples, each containing SANs from 2 hearts.
Table 1: Target genes, encoded proteins, and description of proteins. Genes Proteins Protein descriptions Gap junction proteins Gja1 Cx43 Connexin43 Gja5 Cx40 Connexin40 Gjc1 Cx45 Connexin45 Gjd3 Cx31.9 Connexin31.9 Cell membrane transport Atp1a1 Na/K ATPase, [alpha]1 ATPase, [Na.sup.+]/[K.sup.+] transporting, alpha 1 polypeptide Atp1a2 Na/K ATPase, [alpha]2 ATPase, [Na.sup.+]/[K.sup.+] transporting, alpha 2 polypeptide Atp1a3 Na/K ATPase, [alpha]3 ATPase, [Na.sup.+]/[K.sup.+] transporting, alpha 3 polypeptide Atp1b1 Na/K ATPase, [beta]1 ATPase, [Na.sup.+]/[K.sup.+] transporting, beta 1 polypeptide Atp2b1 Na/K ATPase, [beta]2 ATPase, [Ca.sup.++] transporting, plasma membrane 1 Slc8a1 NCX1 Solute carrier family 8 (sodium/calcium exchanger), member 1 Trpc1 TRPC1 Transient receptor potential channel 1 Trpc3 TRPC3 Transient receptor potential channel 3 Trpc6 TRPC6 Transient receptor potential channel 6 Intercellular [Ca.sup.2+] transport and [Ca.sup.2+] regulation Atp2a2 SERCA2 Sarcoplasmic/endoplasmic reticulum calcium ATPase 2 Calm1 Calm1 Calmodulin 1 Calm3 Calm3 Calmodulin 3 Casq2 Casq2 Calsequestrin 2 Itpr1 IP3R1 Inositol 1,4,5-trisphosphate receptor, type 1 Itpr2 IP3R2 Inositol 1,4,5-trisphosphate receptor, type 2 Itpr3 IP3R3 Inositol 1,4,5-trisphosphate receptor, type 3 Pln PLB Phospholamban Ryr2/RYR2 RYR2 Ryanodine receptor 2 Ryr3/RYR3 RYR3 Ryanodine receptor 3 Hyperpolarization-activated cyclic nucleotide-gated channels Hcn1 HCN1 Hyperpolarization-activated cyclic nucleotide-gated channel 1 Hcn2 HCN2 Hyperpolarization-activated cyclic nucleotide-gated channel 2 Hcn3 HCN3 Hyperpolarization-activated cyclic nucleotide-gated channel 3 Hcn4 HCN4 Hyperpolarization-activated cyclic nucleotide-gated channel 4 Calcium channels Cacna1c Cav1.2 Voltage-dependent, L-type, alpha 1C subunit Cacna1d Cav1.3 Voltage-dependent, L-type, alpha 1D subunit Cacna1g Cav3.1 Voltage-dependent, T-type, alpha 1G subunit Cacna1h Cav3.2 Voltage-dependent, T-type, alpha 1H subunit Cacna2d1 [Ca.sub.v][alpha]2[delta]1 Voltage-dependent, alpha 2/ delta subunit 1 Cacna2d2 [Ca.sub.v][alpha]2[delta]2 Voltage-dependent, alpha 2/ delta subunit 2 Cacna2d3 [Ca.sub.v][alpha]2[delta]3 Voltage-dependent, alpha 2/ delta subunit 3 Cacnb1 [Ca.sub.v][beta]1 Voltage-dependent, beta 1 subunit Cacnb2 [Ca.sub.v][beta]2 Voltage-dependent, beta 2 subunit Cacnb3 [Ca.sub.v][beta]3 Voltage-dependent, beta 3 subunit Cacng4 [Ca.sub.v][gamma]4 Voltage-dependent, gamma subunit 4 Cacng7 [Ca.sub.v][gamma]7 Voltage-dependent, gamma subunit 7 Potassium channels Kcna1 [K.sub.v]1.1 Voltage-gated shaker-related subfamily A, member 1 Kcna2 [K.sub.v]1.2 Voltage-gated shaker-related subfamily A, member 2 Kcna3 [K.sub.v]1.3 Voltage-gated shaker-related subfamily A, member 3 Kcna4 [K.sub.v]1.4 Voltage-gated shaker-related subfamily A, member 4 Kcna5 [K.sub.v]1.5 Voltage-gated shaker-related subfamily A, member 5 Kcnb1 [K.sub.v]2.1 Voltage-gated shab-related subfamily B, member 1 Kcnd1 [K.sub.v]4.1 Voltage-gated shal-related subfamily D, member 1 Kcnd2 [K.sub.v]4.2 Voltage-gated shal-related subfamily D, member 2 Kcnd3 [K.sub.v]4.3 Voltage-gated shal-related subfamily D, member 3 Kcnh2 ERG-1 Ether-A-go-go-related protein 1 Kcnip2 KChIP2 [K.sub.v] channel interacting protein 2 Kcnj11 [K.sub.ir]6.2 Inwardly rectifying subfamily J, member 11 Kcnj12 [K.sub.ir]2.2 Inwardly rectifying subfamily J, member 12 Kcnj14 [K.sub.ir]2.4 Inwardly rectifying subfamily J, member 14 Kcnj2 [K.sub.ir]2.1 Inwardly rectifying subfamily J, member 2 Kcnj3 [K.sub.ir]3.1 Inwardly rectifying subfamily J, member 3 Kcnj5 [K.sub.ir]3.4 Inwardly rectifying subfamily J, member 5 Kcnj8 [K.sub.ir]6.1 Inwardly rectifying subfamily J, member 8 Kcnk1 TWIK1 Two pore domain subfamily K, member 1 Kcnk2 TREK1 Two pore domain subfamily K, member 2 Kcnk3 [K.sub.2P]3.1 Two pore domain subfamily K, member 3 Kcnk5 [K.sub.2P]5.1 Two pore domain subfamily K, member 5 Kcnk6 TWIK2 Two pore domain subfamily K, member 6 Kcnn1 SK1 Calcium/activated intermediate/small conductance subfamily N alpha, member 1 Kcnn2 SK2 Calcium/activated intermediate/small conductance subfamily N alpha, member 2 Kcnn3 SK3 Calcium/activated intermediate/small conductance subfamily N alpha, member 3 Kcnq1 [K.sub.v]7.1 Voltage-gated KQT-like subfamily Q, member 1 Miscellaneous proteins Abcc8 SUR1 ATP-binding cassette transporter subfamily C member 8 Abcc9 SUR2 ATP-binding cassette subfamily C member 9 Nppa ANP Atrial natriuretic peptide Nppb BNP Brain natriuretic peptide Pias3 KChAP Protein inhibitor of activated STAT3 Table 2: General characteristics of GK rats. Control Nonfasting blood glucose (mg/dl) 93.00 [+ or -] 3.28 Fasting blood glucose (mg/dl) 60.60 [+ or -] 1.99 Blood glucose 120 min post 97.10 [+ or -] 2.14 glucose challenge (mg/dl) Body weight (g) 369.10 [+ or -] 7.03 Heart weight (g) 1.26 [+ or -] 0.02 Heart weight/body weight ratio 3.43 [+ or -] 0.04 GK p value Nonfasting blood glucose (mg/dl) 128.50 [+ or -] 5.06 ** 0.001 Fasting blood glucose (mg/dl) 108.75 [+ or -] 4.99 ** 0.001 Blood glucose 120 min post 230.55 [+ or -] 12.69 ** 0.001 glucose challenge (mg/dl) Body weight (g) 414.90 [+ or -] 7.10 ** 0.001 Heart weight (g) 1.37 [+ or -] 0.02 ** 0.001 Heart weight/body weight ratio 3.30 [+ or -] 0.05 * 0.049 Data are mean [+ or -] SEM, n = 10 hearts, ** p < 0.01, * p < 0.05.
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|Title Annotation:||Research Article|
|Author:||Howarth, F.C.; Qureshi, M.A.; Jayaprakash, P.; Parekh, K.; Oz, M.; Dobrzynski, H.; Adrian, T.E.|
|Publication:||Journal of Diabetes Research|
|Date:||Jan 1, 2018|
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