Acute dapagliflozin administration exerts cardioprotective effects in rats with cardiac ischemia/reperfusion injury

All experiments in this study were performed in accordance with guidelines for the care and use of laboratory animals by the NIH. The experimental protocol was approved by the Institutional Animal Care and Use Committee, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand. After 7 days of acclimatization, male Wistar rats (n = 48, 250–300 g, 8 weeks old) underwent cardiac I/R protocols. These rats were subdivided into four groups to enable 4 different treatments (Fig. 1): (1) Pretreated group: dapagliflozin was administered 15 min before cardiac ischemia; (2) Ischemia group: dapagliflozin was administered 15 min into the cardiac ischemic period; (3) Reperfusion group: dapagliflozin was administered at the onset of reperfusion, and 4) Control group: normal saline solution was administered to the rats as a vehicle. Dapagliflozin (Bristol-Myers Squibb and AstraZeneca Co.) was dissolved in 1 ml of normal saline solution, and 1 mg/kg of dapagliflozin was administered via left femoral vein injection. LV function was determined during the I/R protocol using a pressure–volume (P–V) loop (Transonic, USA) [13]. An arrhythmia score was evaluated from a lead II electrocardiogram (ECG). At the end of the I/R protocol, the heart was excised immediately to enable measurement of myocardial infarct size and the study of myocardial tissues.

Rats were anesthetized by administration of Zoletil (50 mg/kg, Virbac, Thailand) and Xylazine (0.15 mg/kg, LBS labs, Thailand) intramuscularly. The level of anesthesia was closely monitored by determination of the respiration pattern, eye and pedal reflexes. The rats were ventilated with room air from a rodent ventilator (Cwe, Inc, Ardmore, PA, USA) after the tracheostomy was done. Lead II ECG was recorded during the study using a PowerLab system with Chart 7.0 program (AD Instrument, Australia). A left-side thoracotomy was operated at the fourth intercostal space, the pericardium was cut to expose the heart. The ligation was performed at the left anterior descending coronary artery (LAD) 0.2 cm distal to its origin. The ST segment elevation on lead II ECG and a color change of the myocardial tissue were used to confirm successful ischemia, and the ischemia was continued for 30 min. Then, the ligature was released to induce reperfusion for 2 h [14, 15].

The incidence of cardiac arrhythmia was determined using the Lambeth Conventions [16]. Arrhythmia scores were evaluated using the criteria described in previous studies [17, 18].

For LV function measurement, the right carotid artery was located and a P–V loop catheter (Transonic, USA) was inserted into the LV to evaluate LV function during the I/R. Heart rate (HR), left ventricular end-systolic and diastolic pressure (LVESP and LVEDP), dP/dt_max, dP/dt_min, stroke volume (SV) and left ventricular ejection fraction (LVEF) were determined using a Labscribe program (Labscribe, USA) [13, 14]. For P–V loop data analysis: (1) 50 loops before ischemia were selected to represent the baseline; (2) 50 loops at the end of coronary occlusion were selected to represent the ischemic period, and (3) 50 loops at the end of reperfusion were selected to represent the reperfusion period.

After 2 h of reperfusion, the rats were sacrificed and the heart was rapidly removed. The LAD was re-occluded and the heart was evaluated the LV area at risk (AAR) by 1 ml Evan’s blue dye perfusion. The heart was kept at − 20 °C overnight and then sectioned horizontally at 1–2 mm thickness. After that, heart slices were immersed in 2,3,5-triphenyltetrazolium chloride (TTC) in phosphate buffer saline solution. The TTC stained area indicated viable tissue which was detected by the red coloration. The infarct size was identified by the white color area that was not stained with any dyes. The myocardial infarct size and the AAR were calculated in accordance with the formula of Reiss et al. using the image tool program [14, 15].

The hearts were washed with cold normal saline solution. Cardiac mitochondria were isolated and collected from both remote and ischemic myocardial tissues [19, 20] to determine cardiac mitochondrial function. Variables recorded including cardiac mitochondrial reactive oxygen species (ROS) levels, cardiac mitochondrial membrane potential changes, and cardiac mitochondrial swelling. An enhancement in the 2′,7′-dichlorofluorescein fluorescent intensity demonstrates an increase in mitochondrial ROS production, which correlates with an increase in oxidative stress levels. An attenuation in the red/green fluorescence intensity ratio of JC-1 dye indicates an increase in mitochondrial membrane depolarization. Finally, an attenuation in mitochondrial absorbance at 540 nm implies mitochondrial swelling [19, 20].

The heart was removed and LAD was re-occluded at the same site that had been previously ligated. Then, it was irrigated with normal saline solution through aorta to remove blood inside coronary arteries in remote area, but not ischemic area. Therefore, the ischemia and remote areas could be observed. After that, the tissues from the ischemic and remote areas were separated, chopped into smaller pieces and homogenized in the isolated heart buffer. The homogenate from each area was centrifuged at 800g for 5 min to collect the supernatant and then centrifuged it at 8800g for 5 min. The pellet was resuspended in the isolated heart buffer and centrifuged at 8800g for 5 min. Isolated mitochondria were collected and the protein concentration were determined using a Bradford protein assay (Bio-Rad Laboratories, USA). Proteins sample of 50–80 μg were mixed with the loading buffer and subjected to gel electrophoresis. Then, the protein extracts were transferred to nitrocellulose membranes in a transfer buffer. Membranes were incubated with either 5% skimmed milk or bovine serum albumin in a tris-buffered saline containing 0.1% tween (TBST) for 1 h at room temperature. The membranes were exposed overnight to primary antibodies including PGC1α, CPT1, mitochondrial oxidative phosphorylation complex I-V, DRP1, MFN2 and OPA1 (Cell Signaling Technology, USA) to determine cardiac mitochondrial biogenesis and dynamics. Additionally, the cardiac apoptotic signaling was determined by using the primary antibodies against caspase-3, cleaved caspase-3, Bax and Bcl2 (Cell Signaling Technology, USA). For cardiac gap junction protein assessment, primary antibodies against connexin-43 (Cx43), and p-Cx43 at serine 368 residue (Cell Signaling Technology, USA) were used. Afterwards, the membranes incubated with horseradish peroxidase were conjugated with anti-rabbit IgG (Cell Signaling Technology, USA). Subsequently, western blot bands were detected and used for the analysis of protein expression [14].

The myocardial apoptosis was determined by terminal deoxynucleotidyl nick-end labeling (TUNEL) assay (Roche, Basel, Switzerland). The cardiac tissue slices were placed in phosphate buffer saline solution for 10 min after dehydration. The slices were incubated with Proteinase k solution (1:50) for 30 min, followed by incubation with CytoninTM for another 120 min. The levels of apoptosis was analyzed as a percentage of the number of TUNEL-positive cells over the total number of DAPI positive cells [21].

In this study, no mortality was observed during cardiac I/R in any groups. Figure 2 shows the size of myocardial infarction. There is no difference in the area at risk between groups (Fig. 2a). The representative heart sections from the control and the intervention groups are shown in Fig. 2b. Dapagliflozin given at pretreatment and during ischemia significantly reduced the myocardial infarction size, compared to controls (Fig. 2b). However, dapagliflozin given at the onset of reperfusion did not exert this benefit. Differential temporal effects of the drug administration on the infarct size can be clearly observed, the size of infarction in rats pretreated with dapagliflozin showing a reduction of ~ 42% in comparison to the control. This is statistically significantly lower than the sizes in rats treated during ischemia (~ 16% reduction).

Figure 3a, b show that the time to 1st VT/VF onset and arrhythmia score in rats pretreated with dapagliflozin was significantly longer, when compared to rats in the control group. Nevertheless, these parameters in the dapagliflozin treatment during ischemia and at the beginning of reperfusion groups were no different from the control group (Fig. 3a, b). In the pretreated group the ratio of Cx43 phosphorylation (pCx43) to total Cx43 was elevated significantly, compared to the control. This was not the case during ischemia and at the beginning of reperfusion groups (Fig. 3c, d).

Figure 4a–g shows alteration in LV function at different time points of I/R injury. At the baseline, there was no difference in parameters between groups. After LAD occlusion, an attenuation in stroke volume, dP/dt_max, dP/dt_min and % left ventricular ejection fraction (LVEF) and an elevation in end diastolic pressure were observed. During ischemic and after reperfusion periods, only the dapagliflozin pretreated group had improved dP/dt_max and %LVEF, when compared with the control group (Fig. 4e, g). Nevertheless, no improvements were seen in any parameters in the groups where dapagliflozin was given during ischemia and at the beginning of reperfusion.

The expression of anti-apoptotic protein Bcl-2, pro-apoptotic protein Bax, caspase 3 and cleaved-caspase 3 are shown in Fig. 5a–d. The Bcl-2 levels in the pretreated group and during ischemia group were significantly increased, when compared to the control group (Fig. 5b). However, the Bax, caspase 3 and cleaved-caspase 3 levels were no different across all groups (Fig. 5a, c, d). The pretreated group and during ischemia group had significantly decreased numbers of TUNEL positive cells, when compared to the control (Fig. 6). Moreover, the TUNEL positive cells were notably attenuated in the pretreated group, compared to the during ischemia group (Fig. 6).

With regard to mitochondrial function, rats in the pretreated group and during ischemia group had significantly decreased reactive oxygen species (ROS) production (Fig. 7a) and increased absorbance intensity, revealing less mitochondrial swelling (Fig. 7c), compared with the control group. However, the red/green fluorescence intensity ratios, demonstrating mitochondrial depolarization, were no different across all groups (Fig. 7b). These findings were also consistent with the significant elevation in CPT1 observed in the pretreated and during ischemia groups, when compared to the control (Fig. 8b). The level of complex I of the electron transport chain increased significantly in all dapagliflozin treated groups (Fig. 8c), compared to the controls. However, the PGC1-α and complex II-V were no different across all groups (Fig. 8a, d–g). In the case of cardiac mitochondrial dynamics, all treatment groups had similarly increased cardiac mitochondrial OPA1 levels (Fig. 9c). However, the cardiac mitochondrial MFN2 and DRP1 levels were no different across all groups (Fig. 9a, b, respectively).

It is known that cardioprotective effects of SGLT-2 inhibitors are due to its systemic effect via glycosuria and natriuresis [22‐26]. However, the benefits of dapagliflozin found in this study could be mainly due to its direct effect on the heart since it was given to the rats only 15 min prior to cardiac I/R injury. Therefore, its direct cardiac mechanisms may clarify the explanation for the findings. From present information, the direct effects of SGLT-2 inhibitors occurred through their ability to attenuate ionic dyshomeostasis, mitochondrial dysfunction, oxidative stress, inflammation and apoptosis in the heart [27].

Our results demonstrated that acute dapagliflozin treatment during cardiac I/R injury exerted cardioprotective benefits. The crucial aspects of the data accrued in this study can be summarized as follows: (1) the improvement in LV function shown by increased %LVEF; (2) a decrease in arrhythmia score and an increase in Cx43 phosphorylation; (3) a decrease in size of infarction, and cell apoptosis (TUNEL positive cells) and an increase in Bcl2 causing anti-apoptotic protein expression; (4) an attenuation of mitochondrial dysfunction occurred in the heart as demonstrated by a reduction in swelling and ROS production; (5) an attenuation of cardiac energy metabolism dysfunction evidenced by an increased expression of CPT1 and mitochondrial complex I of the ETC; and (6) an attenuation of cardiac mitochondrial dynamic imbalance as indicated by increased mitochondrial fusion.

Taken together with the EMPA-REG OUTCOME trial, previous clinical studies showed benefits of SGLT-2 inhibitors on cardiac function in patients with type 2 diabetes, ischemic heart and heart failure [28‐33]. SGLT-2 inhibitors also reduced myocardial oxidative stress, fibrosis and vascular remodeling which play important roles in the pathogenesis of cardiovascular diseases [34, 35]. Focus on cardiac I/R injury, previous studies have primarily aimed to attenuate size of cardiac infarction [7, 8]. Although previous reports have shown the beneficial effects of dapagliflozin pretreatment during I/R injury by lowering myocardial infarct size [11, 12], its effects given after cardiac ischemia were not known. With regard to the clinical benefits in acute myocardial infarction patients, it is essential that any acute pharmacological intervention must provide cardioprotective effects when it is given after myocardial ischemia. Our study established that acute dapagliflozin treatment during cardiac ischemia could still provide cardioprotective effect by reducing the infarct size (~ 16% reduction), even though it was not as effective as pretreatment (~ 42% reduction). The efficacy of the mechanism used by dapagliflozin for attenuation of the size of infarction will be directly related to its capacity to decrease cardiac mitochondrial dysfunction, enhance mitochondrial fusion and attenuate cardiomyocyte apoptosis. Taken together, all of the above benefits of dapagliflozin treatment could explain the improvement in LV dysfunction seen in this study.

In addition to the infarct size and LV function improvement, our results also showed that rats in the dapagliflozin pretreatment group had a delayed time to first VT/VF onset and lower arrhythmia score, when compared to controls. These findings indicated that dapagliflozin exerted an anti-arrhythmic effect during cardiac I/R injury. In addition, its anti-arrhythmic actions could be explained by its effect on Cx43, which is a cardiac gap junction protein promoting cardiac cell communication through electrical current flow [36]. Cx43 at serine 368 phosphorylation has been shown to increase the translocation of Cx43 to the cell membrane, helping with gap junction formation [36]. In this study, dapagliflozin improved gap junction function as evidenced by an increased pCx43 Ser₃₆₈/Cx43 ratio. All of these effects of dapagliflozin could be reasonably assumed to be related to the reduction in arrhythmia found in this study.

It is known that cardiac I/R injury is associated with mitochondrial damage and cardiac cell apoptosis [11, 14]. The mitochondrial damage can occur after 20 min of occlusion and the severity will gradually increase during the reperfusion period [37, 38]. Chronic dapagliflozin treatment for 1 month before cardiac I/R injury in rats with metabolic syndrome lowered the enhancement of mitochondrial ROS production, depolarization and swelling [11]. Our results indicated that the cardiac mitochondrial dysfunction indicated by the increase in mitochondrial ROS production and swelling from cardiac I/R injury were significantly reduced in the acute dapagliflozin pretreatment and during ischemia groups. In the case of mitochondrial biogenesis, PGC1-α and CPT1, which are cardiac mitochondrial metabolism-related proteins, are vital proteins playing roles in cardiac fatty acid oxidation [39, 40]. Our results showed that dapagliflozin treatment increased CPT1 protein expression. Dapagliflozin treatment also elevated complex I of the ETC expression, indicating its action in attenuating the depletion of cardiac energy metabolism when I/R injury occurred.

The maintenance of the number of mitochondria is preserved by the equilibrium between fission and fusion [41]. These cycles keep mitochondria functional by abolishing impaired mitochondria and promoting apoptosis when exposed to stress [42]. The proteins which play roles in helping fusion of the outer and inner membranes are Mitofusin 2 (MFN2) and optic atrophy 1 (OPA1) respectively, whereas the protein which plays roles in membrane constriction during fission is dynamin-related protein 1 (DRP1) [43]. It is known that cardiomyocytes can be preserved during I/R injury and cardiac arrest by using mitochondrial fission inhibitors [44, 45]. A previous study demonstrated that 1-month of dapagliflozin treatment lowered the elevation of cardiac mitochondrial fission and the attenuation of mitochondrial fusion as evidenced by decreased DRP1 and increased MFN2 and OPA1 protein expression in metabolic syndrome rats subjected to cardiac I/R injury [11]. In contrast to chronic treatment, acute administration of dapagliflozin caused no change in the expression of DRP1, a mitochondrial fission protein. However, it increased the expression of OPA1, a mitochondrial fusion protein. Our study showed the benefits of dapagliflozin on mitochondrial dynamics, related expression of proteins, biogenesis and function. These could be the key factors responsible for infarct size attenuation with dapagliflozin treatment.