Introduction
Diabetes mellitus (DM) is a global epidemic with significant adverse impacts on life expectancy and quality of life. More than 170 million people worldwide suffer from diabetes, and this figure is projected to double by the year 2030 [
1]. It is widely recognized that DM is associated with adverse alterations in myocardial structure and function, collectively known as diabetic cardiomyopathy, which is responsible for the development of heart failure in this population [
2‐
4]. One of the hallmarks of diabetic cardiomyopathy is left ventricular diastolic dysfunction, which is often associated with normal systolic function in the early disease processes [
5]. Indeed, the incidence of heart failure with preserved ejection fraction (HFpEF) in diabetes has increased sharply over the past two decades [
6‐
8].
Diastolic dysfunction is characterized by increased myocardial stiffness leading to abnormal left ventricular relaxation that is associated with increased filling pressure. Poor glycemic control adversely affects diastolic function by several mechanisms, including increased oxidative stress, chronic inflammation, myocardial hypertrophy, perivascular and interstitial collagen deposition and cross-linking, abnormal intracellular calcium handling, endothelial and mitochondrial dysfunction and apoptosis [
9‐
12]. The mitochondria are the main sites where reactive oxygen species (ROS) are generated [
13]. Previously, our group found that the atrial tissue of diabetic rabbits showed markedly higher mitochondrial ROS generation rate in contrast with the control group, and the treatment of dipeptidyl peptidase-4 (DPP-4) inhibitor, alogliptin, suppressed their generation and attenuate adverse atrial remodeling [
14]. By contrast, the effects of DPP-4 inhibitors on ventricular function in diabetes are not completely understood. Therefore, in this study, we aimed to investigated the mechanisms by which alogliptin affects ventricular function in early stage of diabetes specifically focusing on the role of the mitochondria.
Methods
Experimental animals and study protocol
This study was approved by the Experimental Animal Administration Committee of Tianjin Medical University and Tianjin Municipal Commission for Experimental Animal Control. Japanese white rabbits (1.8–2.2 kg) were purchased from Beijing Medical Animals Research Institute. A computer was used to generate 30 different random numbers corresponding to every rabbit. The first 10 rabbits were taken as the control group, the middle 10 rabbits as the DM group, and the remaining 10 rabbits as the alogliptin-treated DM (DM-A) group. In each group, echocardiographic, hemodynamic, histological, serum biochemical and oxidative stress–related markers, as well as Western blot and mitochondrial function were determined.
Rabbit model of diabetes mellitus
The alloxan-induced diabetes model using rabbits has been previously used by our group [
15,
16]. Briefly, it involves intravenous injection of 5% alloxan (alloxan monohydrate, Sigma Aldrich Chemical; 120 mg/kg) dissolved in sterile normal saline into the marginal ear vein. This produces a type 1 diabetes mellitus model by damaging the pancreatic beta cells. Fasting blood glucose was measured 48 h later with confirmation of diabetes by glucose levels ≥ 14 mmol/L. If the fasting blood glucose level did not reach diagnostic criteria after 48 h, then the same dose of alloxan was injected again. If this failed to induce diabetes again, then the rabbit was excluded from the study. Fasting blood glucose concentration was monitored weekly using the glucometer Optium Xceed (Abbott Labora-tories MediSense Products). After diabetes was established, animals in the DM-A group were given alogliptin (12.5 mg/kg/day; Tianjin Takeda Pharmaceuticals Co, Ltd) that was mixed into the food for 12 weeks. This dose was selected as it is in keeping with previously used dosing regimen in prior experiments [
17].
Echocardiographic assessment
After 12 weeks, all the rabbits underwent resting transthoracic two-dimensional echocardiography and Doppler imaging to assess left ventricular function by operators blinded to grouping. They were anesthetized with 3% pelltobarbitalum natricum (30 mg/kg), and echocardiographic parameters were obtained in the parasternal long-axis view using a GE Vingmed machine (Vivid 7/Vingmed General Electric) equipped with a 7.5-MHz standard pediatric probe. Standard imaging planes, M-mode, color-mode, Doppler, and functional calculations were acquired according to the guidelines of the American Society of Echocardiography [
18]. Left atrial (LA) anteroposterior diameter, left ventricular posterior wall (LVPW) thickness, interventricular septal thickness (IVS), left ventricular end-diastolic dimension (LVEDD), and left ventricular end-systolic dimension (LVESD) were measured using both 2-dimensional and M-mode imaging during 5 consecutive cardiac cycles. Left ventricular ejection fraction was calculated, and the mean of three measurements was calculated for subsequent analysis. Left ventricular diastolic function was evaluated by the mitral peak velocity of early filling (E) to early diastolic mitral annular velocity (e′) (E/e′) ratio.
Hemodynamic study and sample collection
After echocardiographic examination, each rabbit underwent right carotid artery cannulation for measuring hemodynamic parameters during ECG monitoring. Heart rate (HR), aortic systolic blood pressure (SBP), diastolic blood pressure (DBP), and mean blood pressure (MBP) were recorded carefully after a stabilization period using a BL-420F biological function detection system (Chengdu Taimeng Science and Technology Co, Ltd). Then the cannula was inserted through the aortic valve to the left ventricle to measure the ventricular end-diastolic pressure (LVEDP), maximal and minimal rates (± dp/dtmax) of the rise in left ventricular pressure.
Blood samples were obtained from the carotid artery after hemodynamic examination for measurements of serum biochemical, inflammatory, and oxidative stress markers. The animals were then euthanized and a portion ≈ 100 mg LV tissues were collected for mitochondrial function study immediately. Another about 100 mg LV tissues were frozen in liquid nitrogen, and stored at − 80 °C for western blot. Small pieces of LA tissue were immersed in 10% formaldehyde and 2.5% glutaraldehyde for histological and ultrastructural studies respectively.
Isolation of mitochondria from the left ventricle
LV tissue collected as mentioned above was quickly dissected and minced in an ice-cold isolation medium containing mannitol 220 mmol/L, sucrose 70 mmol/L, HEPES 5 mmol/L, PMSF 1 mmol/L, BSA 0.2% (w/v), and pH 7.4. The minced blood-free tissue was homogenized using a manual glass homogenizer with 6 passes (0–4 °C). The homogenate was centrifuged at 1000×g for 10 min and the liquid supernatant was collected. It was then centrifuged at 10,000×g for 10 min. The major constituent of the deposit was mitochondrial pellet, which was suspended in 0.5 mL of the conversational medium containing mannitol 220 mmol/L, sucrose 70 mmol/L, HEPES 5 mmol/L, and PH 7.4. The mitochondrial isolation procedures were completed within 1 h after the rabbits were euthanized. Mitochondrial protein concentration was quantified using the Bradford colorimetric method.
Mitochondrial respiration
Mitochondrial respiratory function was measured polarographically at 25 °C using a Clark-type oxygen electrode (Oroboros Instruments, Innsbruck, Austria). In a 2-mL closed thermostatic and magnetically stirred glass chamber, respiration medium containing Mannitol 225 mmol/L, Sucrose 70 mmol/L, EDTANa2 1 mmol/L, KH2PO4 20 mmol/L, K2HPO4 20 mmol/L, BSA 1 mg/mL (PH, 7.4) was saturated with ambient oxygen to reach a concentration of 258 μmol/L. After an equilibration period, 300 μg mitochondrial protein was added to the reaction system. When the mitochondrial oxygen consumption was stable, 15 μL mixture of 0.8 mol/L malic acid and 1 mol/L glutamic acid was added to initiate the state 2 respiration. After stable state 2 respiration was established, oxidative phosphorylation was started by the addition of 200 nmol/L ADP. Namely, state 3 respiration was initiated. When all of the ADP had been phosphorylated to ATP, state 4 respiration started. The respiratory control ratio (RCR) was calculated as the ratio of the respiratory rate in state 3 to that in state 4.
Mitochondrial membrane potential
Mitochondrial membrane potential (Δψ) was assessed by tetraethyl benzimidazolyl carbocyanine iodide cationic dye at 37 °C in 2 mL of respiration medium, which exhibited potential-dependent accumulation in mitochondria, resulting in a fluorescence emission shift from 525 nm (green) to 590 nm (red). Theoretically, loss of Δψ was detectable by the decrease in the red to green fluorescence emission ratio. 300 μg mitochondrial protein was added into the respiration medium with tetraethyl benzimidazolyl carbocyanine iodide dye. After equilibration for 10 min, mitochondrial respiratory function was initiated by a 15 μl mixture of 0.8 mol/L malic acid and 1 mol/L glutamic acid, and the alteration of the fluorescence emission was detected.
Mitochondrial reactive oxygen species production
Mitochondrial ROS generation was assessed using fresh mitochondrial suspensions with the dichlorodihydrofluorescein diacetate probe [
19]. Mitochondrial protein 300 μg was added to a quartz cuvette containing 3 mL of phosphate buffer (KCl 130 mmol/L, MgCl
2 43 mmol/L, NaH
2PO
4 20 mmol/L, glucose 30 mmol/L, malate 2 mmol/L, PH 7.4) and 2 μL of 2.5 mmol/L dichlorodihydrofluorescein diacetate which was dissolved in 1.25 mmol/L methanol and kept in the dark at 0 °C. The mixture was incubated at 37 °C for 15 min, and dichlorodihydrofluorescein diacetate formation was determined fluorometrically at the excitation wavelength of 499 nm and emission wavelength of 521 nm at 37 °C for 2 min using a Cary Eclipse Fluorescence spectrophotometer (Varian). The dichlorodihydrofluorescein diacetate fluorescence was normalized to the fold of the control group [
20].
Serum biochemical, inflammatory oxidative stress measurements
Blood samples collected were used for serum biochemical examination, including fasting glucose, total cholesterol, triglyceride, low-density lipoprotein cholesterol (LDL-c), high-density lipoprotein cholesterol (HDL-c) and creatinine level by full automatic biochemical analyzer. Fasting insulin and GLP-1 level were assessed using Rabbit Insulin ELISA Kit (Wuhan Huamei Biological Engineering Co., Ltd, Hubei Province, China) and Rabbit Glucagon Like Peptide-1 ELISA Kit (Shanghai Huding Biological Technology Co., Shanghai, China) according to the manufacturer’s instructions respectively. Serum oxidative stress related markers Lipid Peroxidation Malondialdehyde (MDA) and 8-hydroxy-2 deoxyguanosine (8-OHdG) were assessed by MDA Assay Kit (Nanjing Jianchen Bioengineering Institute, Jiangsu Province, China) and Rabbit 8-OHdG ELISA Kit (Shanghai Huding Biological Technology Co., Shanghai, China). Serum antioxidant enzyme superoxide Jianchen Bioengineering Institute, Jiangsu Province, China). And the inflammation maker high-sensitivity C-reactive protein (hs-CRP) level was detected using Rabbit hs-CRP ELISA KIT (Wuhan Huamei Biological Engineering Co., Ltd, Hubei Province, China).
Histological and ultrastructural analyses
The LV myocardium was cut at 4-µm intervals and stained with Masson’s trichrome stain to evaluate the extent of interstitial fibrosis. Five Masson staining sections from each myocardium were selected, and in each section, five random sampled areas were studied at 400× field of view. Briefly, to quantify the areas of interstitial fibrosis in the LV myocardium, the blue pixel content of the digitized images, excluding the perivascular fibrotic areas, were measured relative to the total tissue area using Image Pro Plus 6.0 Scion image software (Scion Corporation). LV tissues that have been fixed in 2.5% glutaraldehyde for 2 h were used for ultrastructural analysis. After further fixated in 1% osmium tetroxide, dehydrated in ethanol, and embedded in Epon, ultrathin sections were cut from each sample.
Finally, each ultrathin section was counterstained with uranium acetate and lead citrate, and evaluated under H-7650 transmission electron microscope (Hitachi).
Western blot analysis
Western blotting was performed to assess the expression of transforming growth factor-β1 (TGF-β1) and nuclear factor kappa B (NF-κB) P65, as well as the proteins about mitochondrial biogenesis in three groups. LV tissue protein was extracted by lysis buffer containing 150 mmol/L sodium chloride, 10 mmol/L Tris, 0.01 mol/L EDTA 4 Na, 1% NP40, 10 μg/mL Aprotein, 10 μg/mL leupeptin, 1 mmol/L PMSF, 1 mmol/L Na3VO4, 10 mmol/L NaF. The lysates were centrifuged at 12,000×g for 20 min, and the supernatants were collected. The protein content was assayed using a BCA protein assay reagent kit (Thermo Scientific, USA). Total protein was fractionated by electrophoresis and transferred onto PVDF sheets (Millipore, USA) and separately incubated with a specific antibody targeting transforming growth factor-β1 (TGF-β1) (1:5000; Abcam, USA), nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) P65 (1:1000; Abcam, USA), Peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) (1:1000; Abcam, USA), transcription of nuclear respiratory factors 1 (NRF1) (1:1000; Abcam, USA), mitochondrial transcription factor A (Tfam) (1:1000; Abcam, USA), followed by incubation with appropriate peroxidase-conjugated secondary antibodies. The reactions were visualized using Tanon 5200 Multi Chemiluminescent Imaging System (Tanon Science & Technology Co., Ltd, Shanghai, China).
Statistical analysis
Statistical analysis was performed using SPSS 19.0 statistical software. Data were presented as mean ± standard deviation. Comparisons among the three groups were analyzed for statistical significance using the one-way analysis of variance (ANOVA) followed by Bonferroni correction for comparisons between two groups respectively. A P value < 0.05 was considered statistically significant.
Study limitations
Several limitations of the present study should be acknowledged. Firstly, as we only used one medication of the DPP-4 inhibitor class, further studies are needed whether the effects of alogliptin represent a class effect. Secondly, we did not examine calcium handling and cellular apoptosis, which could contribute to the pathogenesis of diabetic cardiomyopathy. Thirdly, the extent to which the angiotensin II pathway, which is known to induce fibrosis, played a role remains uncertain. Fourthly, Cmax of alogliptin was not measured in our study. Moreover, biomarkers such as B-type natriuretic protein and advanced glycation products, and parameters such as Hba1c, were also not measured. Finally, it is unclear the extent to the improved diastolic function can be attributed to better glycemic control. Further studies can examine whether electrophysiological abnormalities observed in diabetes can be prevented by alogliptin.
Authors’ contributions
XWZ and ZWZ conducted the experiments, analysed the data and drafted the manuscript. YJY, YS, RML, JCQ, YGZ, NJ conducted the experiment, CLL and GT revised the manuscript, GPL and TL designed the experiment and revised the manuscript. All authors read and approved the final manuscript.