Inhibition of dynamin-related protein 1 protects against myocardial ischemia–reperfusion injury in diabetic mice
- Mingge Ding†1, 2,
- Qianqian Dong†3,
- Zhenghua Liu†4,
- Zheng Liu4,
- Yinxian Qu1,
- Xing Li2,
- Cong Huo2,
- Xin Jia2,
- Feng Fu4Email author and
- Xiaoming Wang2Email author
© The Author(s) 2017
Received: 25 November 2016
Accepted: 31 January 2017
Published: 7 February 2017
Many cardioprotective pharmacological agents failed to exert their protective effects in diabetic hearts subjected to myocardial ischemia/reperfusion (MI/R). Identify the molecular basis linking diabetes with MI/R injury is scientifically important and may provide effective therapeutic approaches. Dynamin-related protein 1 (Drp1)-mediated mitochondrial fission plays an important role in MI/R injury under non-diabetic conditions. Importantly, recent studies indicated that Drp1-mediated mitochondrial fission is enhanced in the myocardium of diabetic mice. The above evidences suggested that Drp1 may be one critical molecule linking diabetes with MI/R injury. We hypothesized that inhibition of Drp1 may be effective to reduce MI/R injury in diabetic hearts.
High-fat diet and streptozotocin-induced diabetic mice were subjected to MI/R or sham operation. Mdivi-1 (1.2 mg/kg), a small molecule inhibitor of Drp1 or vehicle was administrated 15 min before the onset of reperfusion. Outcome measures included mitochondrial morphology, mitochondrial function, myocardial injury, cardiac function and oxidative stress.
Mitochondrial fission was significantly increased following MI/R as evidenced by enhanced translocation of Drp1 to mitochondria and decreased mitochondrial size. Delivery of Mdivi-1 into diabetic mice markedly inhibited Drp1 translocation to the mitochondria and reduced mitochondrial fission following MI/R. Inhibition of Drp1 in diabetic hearts improved mitochondrial function and cardiac function following MI/R. Moreover, inhibition of Drp1 reduced myocardial infarct size and serum cardiac troponin I and lactate dehydrogenase activities. These cardioprotective effects were associated with decreased cardiomyocyte apoptosis and malondialdehyde production and increased activities of antioxidant enzyme manganese superoxide dismutase.
Pharmacological inhibition of Drp1 prevents mitochondrial fission and reduces MI/R injury in diabetic mice. The findings suggest Drp1 may be a potential novel therapeutic target for diabetic cardiac complications.
KeywordsDrp1 Mitochondrial fission Diabetes Ischemia–reperfusion
It has been widely recognized that cardiovascular disease is the primary cause of death among diabetic subjects. Patients with diabetes face an increased risk of morbidity from ischemic heart disease than non-diabetic population, with exacerbated myocardial injury and cardiac dysfunction following ischemia/reperfusion (I/R) [1–3]. Moreover, ischemic precondition and many cardioprotective pharmacological agents failed to exert their protective effects in diabetic ischemic hearts [4–6], which means many interventions that are effective in reducing myocardial ischemia/reperfusion (MI/R) injury are ineffective under diabetic condition. Therefore, identify the molecular basis linking diabetes with MI/R injury is scientifically important and may provide effective therapeutic approaches. As mitochondria have been considered as vital cell organelles in cardiomyocytes due to their pivotal role in ATP production required for myocardial contraction and survival, targeting mitochondrial pathological alterations may be one promising strategy against diabetic ischemic injury [7–9].
Recent studies indicate that mitochondria are dynamic organelles that undergo fission and fusion events, which serve to distribute mitochondria to daughter cells, to remove damaged mitochondria, and to help modulate cellular response to stress [10, 11]. Increased mitochondrial fission in the I/R heart has been demonstrated to contribute to reactive oxygen species (ROS) production and infarct generation, while inhibiting mitochondrial fission reduces myocardial injury and improves cardiac function following I/R [12, 13]. Dynamin-related protein 1 (Drp1) is a cytosolic protein that is recruited over the mitochondrial surface to initiate fission through interaction with binding partners as fission protein 1 (Fis1) . Drp1 is translocated to mitochondria in models of myocardial I/R, resulting in mitochondrial fission and dysfunction. Inhibition of Drp1 has been demonstrated to reduce mitochondrial fission and infarct size during I/R injury in non-diabetic animals [13, 15]. These studies suggest that Drp1-mediated mitochondrial fission plays an important role in myocardial ischemia/reperfusion (MI/R) injury under non-diabetic conditions.
Diabetes has a direct effect on mitochondrial dynamics. Mitochondria become shorter and smaller under acute hyperglycemic conditions in a rapid response, which is also mediated by the fission protein Drp1 . Increased mitochondrial fission associated with activated Drp1 is observed in coronary endothelial cells or cardiac myocytes from murine diabetic models [17, 18]. These studies indicate that Drp1-mediated mitochondrial fission is enhanced in diabetic hearts. The above evidences suggested that Drp1 may be one critical molecule linking diabetes with MI/R injury. Then, we hypothesized that inhibiting Drp1-mediated mitochondrial fission may reduce MI/R injury and improve cardiac function under diabetic conditions. The aims of this study were (1) to investigate whether an inhibitor of Drp1 was effective in reducing MI/R injury in diabetic animals, and if so, (2) further explore the underlying mechanisms.
Induction of type 2 diabetic mice
All animal experiments were performed in compliance with the National Institutes of Health Guidelines on Animal Research. All experimental procedures were approved by the Fourth Military Medical University Ethics Committee. The high-fat diet (HFD) and streptozotocin (STZ)-induced diabetic mouse model was developed according to previous studies from our lab and others [19, 20]. Male C57BL/6 J mice (8–10 weeks old) were fed with HFD (D12492, Research Diets) containing 60% fat (kcal%), 20% protein, and 20% carbohydrate for 4 weeks and then injected with a single low dose STZ (90 mg/kg, Sigma, St. Louis, MO, USA) intraperitoneally. One week after STZ injection, mice were considered to have developed diabetes and used for the study only if their 12-h fasting blood glucose levels were higher than 11.1 mmol/L. The successful rate of diabetic model was 91.4% (64 of 70 total mice). Fasting blood samples were collected to analyze serum TG (triacylglycerol) and insulin levels. The level of serum TG was analyzed using an automatic biochemical analyzer (Advia 2400, Siemens, Germany). Serum insulin level was determined by using an enzyme linked immunosorbent assay.
Myocardial ischemia–reperfusion model
Diabetic mice were randomly assigned to receive either mdivi-1 (1.2 mg/kg), a small molecule inhibitor of Drp1 or vehicle (dimethyl sulfoxide) 15 min before the onset of myocardial reperfusion by intraperitoneal injection. The dose and route of mdivi-1 administration were chosen based on previous studies [15, 21, 22] and validated in our preliminary experiments.
Subcellular fractionation and western blotting analysis
Whole-cell lysates and mitochondrial fractions were obtained from mice hearts in different groups. Whole cell lysates were prepared as previously described . Mitochondrial fractions were prepared by using the Mitochondria Isolation Kit (Beyotime Biotechnology, Jiangsu, China). Western blot analysis was performed as previously described . The following primary antibodies were used: anti-Drp1 (Abcam), anti-VDAC1 (Abcam), and anti-GAPDH (Wuhan Boster Biological Technology).
Transmission electron microscopy
Ventricular samples were obtained from the proximal territory to artery occlusion site after 3 h of reperfusion. Samples were fixed in 2.5% glutaraldehyde in 0.1 M sodium cacodylate buffer (pH 7.2) overnight at 4 °C and processed as described before . Images were collected using a JEM-1230 transmission electron microscope (JEOL Ltd., Tokyo, Japan) at 300 kV with a charge-coupled device (CCD) camera. Mitochondrial morphology was analyzed by using Image-Pro Plus software. For each heart, a minimum of 600 mitochondria was subjected to morphometric analysis. The percentage of mitochondria that fell into three size categories (smaller than 0.6 μm2, within 0.6–1.0 μm2, larger than 1.0 μm2) was analyzed in a given field according to previous studies [21, 25].
Determination of mitochondrial function
Mitochondrial electron transport chain complex (I–IV) activities were measured by using specific commercial kits (Shanghai GENMED Technology Co., LTD, China) according to the standard protocols. Intracellular ATP content was determined using ATP bioluminescent assay kits (Biovision) according to manufacturer’s protocols.
Assessment of cardiac function and myocardial infarct size
Cardiac function was measured by invasive hemodynamic evaluation methods at 3 h post-reperfusion as previously described . After 24 h of reperfusion, echocardiography was conducted with a VEVO 2100 platform (Visual Sonics, Toronto, Canada). M-mode images were used to obtain left ventricular end-systolic volume (LVESV) and left ventricular end-diastolic volume (LVEDV) measurements and to calculate the percent ejection fraction (%EF). After echocardiographic examination, myocardial infarct size (IS) was assessed by Evans blue/triphenyl tetrazolium chloride (TTC) double staining and calculated as a percent of infarcted area over total area-at-risk (% INF/AAR) as described before [27, 28].
Determination of serum cardiac troponin I (cTnI) and lactate dehydrogenase
Blood samples were collected from the carotid artery after 3 h of reperfusion period. Serum cardiac troponin I (cTnI) and lactate dehydrogenase (LDH) levels were measured by using specific commercial kits (Nanjing jiancheng Reagents, China). The activities of these two enzymes were presented as nanogram per milliliter (ng/ml) and units per liter (U/L) respectively.
Quantification of cardiomyocyte apoptosis
After 3 h of reperfusion, terminal deoxynucleotidyl nick-end labeling (TUNEL) assay was used to detect cardiomyocyte apoptosis. TUNEL staining was performed as described previously using in situ cell death detection kits (Roche) . The apoptosis index was expressed as the number of apoptotic cells (TUNEL-positive staining)/the total number of nucleated cells (4′,6-diamino-2-phenylindole staining) ×100%. Myocardial caspase-3 activity was measured to detect cardiomyocyte apoptosis with the use of caspase colorimetric assay kits (Chemicon, Temecula, CA, USA) as we described before .
Quantification of malondialdehyde (MDA) and manganese superoxide dismutase activity (MnSOD)
The MDA levels in myocardial homogenates were determined as described before . MnSOD activities were measured spectrophotometrically by using commercial kits (Beyotime, Jiangsu, China) according to manufacturer’s protocols.
All the data are presented as mean ± standard error of the mean (SEM). The differences of all measured parameters were assessed by One-way ANOVA followed by Bonferroni post hoc test with the use of GraphPad Prism software version 5.0. Probabilities of <0.05 were taken as statistically significant.
Characterization of animals
Characterization of animals
Blood glucose (mmol/L)
4.6 ± 0.7
15.8 ± 2.3**
Serum insulin (mIU/L)
15.8 ± 2.1
13.2 ± 3.4
Serum TG (mmol/L)
0.46 ± 0.11
1.32 ± 0.18**
Body weight (g)
25.3 ± 2.5
28.8 ± 3.1
Mdivi-1 inhibited Drp1 translocation to the mitochondria and reduced mitochondrial fission following I/R in diabetic hearts
To determine whether changes in mitochondrial morphology were associated with Drp1 activation following MI/R, we isolated and prepared proximal areas to artery occlusion site for transmission electron microscopy. More mitochondria per μm2 were observed in I/R hearts compared to sham-operated hearts (P < 0.05, Fig. 2c, d). Moreover, there was a significant increase in the percentage of mitochondria smaller than 0.6 μm2 in diabetic vehicle-treated MI/R hearts compared to diabetic sham-operated hearts (39.2 ± 2.1 vs. 18.1 ± 1.5% in Sham group, P < 0.01, Fig. 2d, e), suggesting enhanced mitochondrial fission. Diabetic MI/R mice treated with Mdivi-1 displayed reduced levels of mitochondrial fission compared to vehicle-treated mice as evidenced by decreased number of mitochondria per μm2 and decreased percentage of mitochondria smaller than 0.6 μm2 (12.1 ± 1.6 vs. 39.2 ± 2.1% in MI/R group, P < 0.01, Fig. 2d, e). There was no significant difference in the percentage of mitochondria bigger than 1 μm2 among all the groups. The reason for this may be that elongated mitochondria are more resistant to MI/R injury than middle mitochondria. These findings suggested that Drp1-mediated mitochondrial fission was enhanced in diabetic MI/R hearts, and inhibition of Drp1 reduced mitochondrial fission in diabetic animals following MI/R.
Drp1 inhibition improved mitochondrial function in diabetic MI/R mice
Drp1 inhibition improved cardiac function in diabetic MI/R mice
Drp1 inhibition attenuated MI/R injury in diabetic mice
Drp1 inhibition reduced oxidative stress in diabetic MI/R mice
In this study, we demonstrate for the first time that Drp1-mediated mitochondrial fission is increased following MI/R under diabetic conditions and that its inhibition with Mdivi-1 reduces MI/R injury and improves cardiac function. These findings, coupled with Mdivi-1’s preservation of mitochondrial function and reduction of oxidative stress, indicate an important pathological role of Drp1-mediated mitochondrial fission in diabetic MI/R injury. The findings suggest that Drp1 inhibition may represent a promising novel therapy for diabetic cardiac complications.
It has been demonstrated that mitochondrial dynamics plays an important role in determining mitochondrial morphology and function . However, this important issue has only begun to be addressed in cardiomyocytes during recent years, possibly due to the general perception that spatial constraint of the myofibril architecture in adult ventricular cardiomyocytes may prevent mitochondrial dynamics. Interestingly, the proteins mediating mitochondrial dynamics are abundant in cardiac tissue, suggesting their important roles in cardiac homeostasis [36, 37]. In this study, we showed that I/R induced significant myocardial injury and cardiac dysfunction in diabetic mice, which was accompanied by increased Drp1 activation and mitochondrial fission. Ong et al. have demonstrated that Mdivi-1 administrated 15 min before myocardial ischemia protects the heart against myocardial ischemia/reperfusion (MI/R) injury under non-diabetic conditions . It is important to note that MI/R injury is an acute and unpredictable event. Treatment remedy given at the time of reperfusion reduces MI/R injury would be more meaningful to mimic clinical scenario. In the present study, Mdivi-1 was administrated 15 min before the onset of reperfusion, which may have better translational relevance to the clinical context. Moreover, Mdivi-1 sufficiently prevented mitochondrial fission and reduced MI/R injury in diabetic mice as indicated by decreased serum cTnI/LDH activities and infarct size. To the best of our knowledge, this is the first study not only to find that inhibition of Drp1 reduced MI/R injury under diabetic conditions, but also to reveal that how MI/R injury was reduced (decreased myocardial necrosis and apoptosis and oxidative stress) and how accompanying functional status was changed (improved mitochondrial function and cardiac function) in vivo. Our study extends Ong et al.’s findings and suggests that inhibition of Drp1 may have therapeutic effects for diabetic patients already diagnosed with ischemic heart disease. Targeting other proteins involved in mitochondrial fission may also have cardioprotective effects. Inhibition of the interaction between Drp1 and mitochondrial fission protein 1 (Fis1) using P110 has been showed to reduce myocardial injury following MI/R  and may be a promising target for future studies on diabetic cardiac complications.
Mitochondrial fission is associated with most forms of cell death, while mitochondrial fusion protects against apoptosis . Several studies of multiple apoptotic systems revealed that there were causal links between mitochondrial fission and the induction of cell death [10, 40]. During apoptosis, mitochondria become fragmented, which is dependent on the translocation of Drp1 from cytosol to mitochondria . We have found increased Drp1 translocation to the mitochondria was accompanied by enhanced myocardial apoptosis in I/R myocardium of diabetic animals. Moreover, inhibition of Drp1 significantly suppressed myocardial apoptosis as evidenced by decreased TUNEL-positive cells and caspase-3 activity. Our data suggest that Drp1-mediated mitochondrial fission plays a pivotal role in myocardial apoptosis, a major form of cell death following I/R.
Numerous studies have demonstrated the frequent appearance of dysfunctional mitochondria in diabetes and MI/R injury. Mitochondrial functional damage may lead to detrimental consequences on cardiac function and are considered to play an important role in the pathogenesis of cardiovascular disease [42, 43]. In accordance, our study identified that mitochondrial function was significantly impaired by I/R in diabetic hearts, as evidenced by decreased complex I/II/III/IV activities and ATP content. Mdivi-1 effectively rescued electron transport chain (ETC) activities and ATP content. These results indicated that inhibition of mitochondrial fission preserved mitochondrial function in diabetic I/R hearts, which may contribute to the improved recovery of cardiac function as above.
In addition to ATP production, mitochondrial ETC has been recognized as a major source of ROS in cardiomyocytes. It has been demonstrated that mitochondrial dysfunction caused increased ROS generation [44, 45]. In this study, we assessed MDA production and MnSOD activity as surrogate markers of oxidative stress. There was increased MDA production and decreased MnSOD activity following MI/R in diabetic mice. Mdivi-1 treatment increased MnSOD activity and reduced MDA formation in diabetic I/R hearts, indicating that Drp1 inhibition is effective to suppress I/R-induced oxidative stress in diabetic animals. The implied increased ROS following diabetic MI/R injury is generally known and similar to other studies [46–48], but its amelioration with a Drp1 inhibitor following MI/R under diabetic conditions is novel. Since we have provided evidence that Mdivi-1 can rescue the activities of mitochondrial ETC, it is suggested that inhibition of Drp1 may inhibit ROS production directly at the source.
It needs to point out that this study has some limitations. First, we investigated the effects of Drp1 inhibition in a high-fat diet and streptozotocin-induced diabetic model. The efficacy of Mdivi-1 in other diabetic models such as ob/ob mice remains to be studied. Second, Mdivi-1 was used as one pharmacological inhibitor of Drp1 in this study. Our results need to be confirmed with the use of Drp1 conditional knockout mice or Drp1 dominant-negative adenoviruses. Third, our study mainly investigated the effects of Mdivi-1 in vivo. The complex underlying mechanisms mediating the protective effects need to be further explored in vitro.
The present study demonstrated a critical role of Drp1 in regulating mitochondrial fission and myocardial injury in diabetic mice undergoing MI/R. Pharmacological inhibition of Drp1 prevents mitochondrial fission and reduces MI/R injury in diabetic mice. Our findings suggest that inhibition of Drp1 may be a potential novel therapeutic target for diabetic patients with ischemic heart disease.
cardiac troponin I
dynamin-related protein 1
electron transport chain
fission protein 1
left ventricular end-diastolic volume
left ventricular end-systolic volume
myocardial ischemia and reperfusion
manganese superoxide dismutase
phosphate buffer solution with Tween-20
reactive oxygen species
terminal deoxynucleotidyl nick-end labeling
voltage-dependent anion channel 1
FF and XMW conceived and designed the study. MGD, QQD, ZHL, ZL, YXQ, XL, CH, XJ and FF conducted the research. MGD, FF and XMW analyzed the data. FF and XMW wrote the manuscript. All authors read and approved the final manuscript.
We appreciate all colleagues of the Department of Geriatrics and the Department of Physiology (Fourth Military Medical University, Xi’an) for their excellent technical assistance.
The authors declare that they have no competing interests.
Availability of data and materials
Not applicable. The conclusions of the manuscript are based on relevant data sets available in the manuscript.
Consent for publication
Not applicable. This manuscript does not contain data from any individual person.
Ethics approval and consent to participate
This study was performed in compliance with the National Institutes of Health Guidelines on Animal Research (NIH Publication No. 85–23, revised, 1996), and approved by the Fourth Military Medical University Ethics Committee.
This study was supported by the grants from National Natural Science Foundation of China (No. 81600235, No. 81670354) and Key Project of Natural Science Foundation of Shaanxi, China (2016ZDJC-13) and National Natural Science Foundation of China (No. 81270169).
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