Inhibition of dipeptidyl peptidase-IV enzyme activity protects against myocardial ischemia-reperfusion injury in rats
- Sarah Chua†1,
- Fan-Yen Lee†2,
- Tzu-Hsien Tsai1,
- Jiunn-Jye Sheu2,
- Steve Leu3,
- Cheuk-Kwan Sun4,
- Yung-Lung Chen1,
- Hsueh-Wen Chang5,
- Han-Tan Chai1,
- Chu-Feng Liu4,
- Hung-I Lu1, 2Email author and
- Hon-Kan Yip1, 3, 6Email author
© Chua et al.; licensee BioMed Central. 2014
Received: 26 July 2014
Accepted: 4 December 2014
Published: 13 December 2014
We investigated whether attenuating dipeptidyl peptidase-IV (DPP4) enzyme activity protected rat heart from ischemia-reperfusion (IR) injury (40-min left anterior descending coronary artery ligation followed by 72 h reperfusion).
Methods and results
Adult male Fischer 344 rats (n = 24) were equally divided into sham-control (WT-SC), WT-IR, and WT-IR-Sita (oral sitagliptin 400 mg/kg/day for 3 days) groups, whereas adult male DPP4-deficiency (DPP4D) rats (n = 16) were equally divided into DPP4D-SC and DPP4D-IR groups. Animals were sacrificed at 72 h after reperfusion with collection of heart specimens. Infarct area (H&E), collagen deposition (Sirius-red stain), fibrotic area (Masson's trichrome), and fluorescent-ROS intensity (H2DCFDA-labeling myocardium) of left ventricle were significantly higher in WT-IR than those in other groups, significantly higher in WT-IR-Sita and DPP4D-IR groups than in WT-SC and DPP4D-SC groups (all p < 0.001), but there was no difference between the latter two groups. Protein expressions of oxidative stress (oxidized protein), reactive oxygen species (NOX-1, NOX-2), inflammation (TNF-α, NF-κB, MMP-9, VCAM-1), apoptosis (mitochondrial Bax, cleaved caspase-3 and PARP), myocardial damage markers (cytosolic cytochrome-C, γ-H2AX), and number of inflammatory cells (CD14+, CD68+, CD40+ cells) showed a pattern identical to that of histological changes among all groups (all p < 0.005), whereas markers of anti-apoptosis (Bcl-2) and mitochondrial integrity (mitochondrial cytochrome-C) as well as left ventricular ejection fraction showed an opposite pattern (all p < 0.001). Protein expressions of anti-oxidants (HO-1, NQO-1), angiogenesis factors (SDF-1α, CXCR4), and glycogen-like-peptide-1-receptor were significantly higher inWT-IR-Sita and DPP4D-IR than those in other groups (all p < 0.001).
Abrogation of DPP4 activity protects against myocardial IR injury and preserved heart function.
KeywordsIschemia-reperfusion injury Dipeptidyl peptidase-IV (DPP4) enzyme Sitagliptin Inflammation Oxidative stress Heart function
Myocardial ischemia-reperfusion (IR) injury contributes to adverse cardiac events after myocardial ischemia, cardiac surgery, cardiogenic shock, or circulatory arrest of different -. Despite reperfusion of the ischemic myocardium during primary percutaneous coronary intervention (PCI) is essential to minimize myocardial damage, reperfusion is also well-known for its deleterious effects  due to the generations of oxidative stress, reactive oxygen species (ROS), and vigorous inflammatory and immune reactions ,-. Of particular importance is that the ROS generated interacts with important proteins, such as ion channels, sarco-endoplasmic reticulum, calcium-release channels, and myofilament proteins which are associated with the excitation-contraction coupling. Alterations of the structures of these proteins can change their activities or their susceptibility to proteolysis. Studies have also shown that ROS are a major contributor to the opening of the mitochondrial permeability transition pore, causing the release of cytochrome c and other factors that can lead to hypercontracture and cell death . This reaction ultimately causes loss of heart contractile function and alterations in the cardiovascular system ,. Despite decades of intensive research, advanced pharmaco-therapeutic strategies, and state-of-the-art PCI procedure, there is still no effective treatment for myocardial IR injury.
Growing data have shown that glycogen-like peptide-1 (GLP-1) has inhibitory properties against inflammation and the generations of oxidative stress and ROS -. Additionally, GLP-1 receptor (GLP-1R) has been identified in many organs, including the brain, kidney, digestive organs, and probably also the ,,. This bioactive receptor has been shown to be upregulated in the setting of IR injury . Dipeptidyl peptidase-IV (DPP4), a membrane-anchored ecto-protease, has been identified as leukocyte antigen CD26. Since GLP-1 is the substrate of DPP4 enzyme that can cleave circulating GLP-1, inhibition of DPP4 enzyme activity by sitagliptin, a drug for the treatment of type II diabetes mellitus and a DPP-IV inhibitor, has been reported to enhance the circulating GLP-1 level ,- which has also been found to be increased in DPP4-deficient animals and in acute kidney IR injury ,. Sitagliptin, therefore, may offer cardiovascular protection through increasing circulating GLP-1 levels, thereby suppressing inflammation, oxidative stress, and the formation of atherosclerosis . Accordingly, it is reasonable to believe that sitagliptin therapy may play a crucial role in protecting the heart from acute IR injury.
We have recently demonstrated extremely low DPP4 enzyme activity in DPP4-deficient animals . In fact, DPP4-deficient rats are Fischer 344 rats with mutation of the DPP4 gene. Hence, it is rational to hypothesize that DPP4-deficient rats might be less vulnerable to IR-induced myocardial damage compared to the wide-type Fischer 344. We then further validated this hypothesis by investigating the effect of sitagliptin, a DPP4 inhibitor, on myocardial IRI in an experimental setting.
Materials and methods
All animal experimental procedures were approved by the Institute of Animal Care and Use Committee at Chang Gung Memorial Hospital – Kaohsiung Medical Center (Affidavit of Approval of Animal Use Protocol No. 2010122405) and performed in accordance with the Guide for the Care and Use of Laboratory Animals (NIH publication No. 85–23, National Academy Press, Washington, DC, USA, revised 1996).
Animal grouping and induction of acute myocardial ischemia-reperfusion injury
Pathogen-free, adult male Fischer 344 (i.e., wide type) rats (n = 24) weighing about 300-325 g (Charles River Technology, BioLASCO, Taiwan) were equally categorized into sham controls (WT-SC, n = 8), acute myocardial IR injury only (WT-IR, n = 8), and IR + oral sitagliptin (400 mg/kg) at post-IR 1, 24 and 48 h (WT-IR-Sita, n = 8). Additionally, adult male DPP4-deficiency rats (DPP4D, i.e., DPP4 mutant of Fischer 344; n = 16) weighing about 300-325 g (Charles River Technology, BioLASCO, Taiwan) were equally divided into sham control (DPP4D-SC, n = 8) and DPP4D-IR (n = 8). The dose-titration study which has been performed in our recent reports ,, identified that sitagliptin (400 mg/kg/per day) was the suitable dose for protecting animals in setting of critical limb ischemia and acute kidney ischemia-reperfusion injury. Accordingly, the dosage of sitagliptin (400 mg/kg) which was utilized in the present study was basic on our previous studies ,,. The time point of ischemia-reperfusion injury and sitagliptin treatment were basic on our previous reports with some modification ,.
All animals were placed in a supine position under anesthesia with 2.0% inhalational isoflurane on a warming pad at 37°C for the IR procedure. Under sterile conditions, the heart was exposed via a left thoracotomy. IR injury was induced in WT-IR, WT-IR-Sita, and DPP4D-IR animals by tightening left coronary artery for 40 minutes 3 mm distal to the margin of left atrium with a 7–0 prolene suture. Regional myocardial ischemia was verified by observing a rapid color change from pink to dull red over the anterior surface of the left ventricle and rapid development of akinesia and dilatation over the affected region. Rats receiving thoracotomy only without ischemia induction served as sham controls. The knot was then relieved after 40-minute ischemia, followed by 72 h reperfusion. The rats were sacrificed at 72 h after IR procedure, and hearts were harvested for individual study. The blood was collected from each animal for measuring the circulating level of GLP-1 by ELISA method using a commercialized kit. The dosages of sitagliptin to be utilized in this experiment were based on our recent report , with some modifications.
Functional assessment by echocardiography
Transthoracic echocardiography was performed in each group prior to and on day 3 after myocardial IR induction. The procedure was performed by an animal cardiologist blind to the experimental design using an ultrasound machine (Vevo 2100, Visualsonics). M-mode standard two-dimensional (2D) left parasternal-long axis echocardiographic examination was conducted. Left ventricular internal dimensions [end-systolic diameter (ESD) and end-diastolic diameter (EDD)] were measured at mitral valve and papillary levels of left ventricle, according to the American Society of Echocardiography leading-edge method using at least three consecutive cardiac cycles. Left ventricular ejection fraction (LVEF) was calculated as follows: LVEF (%) = [(LVEDD3-LVEDS3)/LVEDD3] × 100%.
Procedure and protocol for measurement of reactive oxygen species (ROS)
For determining the fluorescent intensity of ROS in myocardium, four additional animals were utilized in each study group. The protocol and detailed procedure of this test were based on our previous report . By the end of study period (i.e., at 72 h after IR procedure), 2′,7′-dichlorodihydrofluorescin diacetate (H2DCFDA, Molecular Probes) was dissolved in DMSO at a concentration of 25 mg/mL. After being diluted with 50% ethanol to a final concentration of 2.5 mg/mL, it was administered intravenously at a dose of 6 μg/gm body weight to each animal. The rats were sacrificed 30 minutes following H2DCFDA administration.
The hearts were excised and sectioned at a level between the ligation and the apex. Totally three 2 mm-thick sections were obtained from each heart. All sections were examined under fluorescent microscope under a magnification of 100×. Both captured fluorescence and gray photos were assessed by using DP controller 184.108.40.206 (Olympus). Gray photos for measuring the fluorescence intensity were processed by using Image J 1.37v (National Institutes of Health, USA). Three gray photos from each section were randomly obtained, giving a total of nine photos for each animal. As compared with the area of increased fluorescence intensity (IFI), the baseline fluorescence intensity (BFI) [arbitrary unit/400 × high-power field (HPF)] was defined as that in myocardium without H2DCFDA. Six BFI areas were measured from each gray photo, from which three BFI areas were randomly chosen. The mean IFI and mean BFI were then calculated. The ratio of IFI to the BFI was determined as the relative fluorescence intensity.
Western blot analysis of heart tissue
The procedure and protocol for Western blot analysis were based on our recent reports ,. Briefly, equal amounts (50 μg) of protein extracts were loaded and separated by SDS-PAGE using acrylamide gradients. After electrophoresis, the separated proteins were transferred electrophoretically to a polyvinylidene difluoride (PVDF) membrane (Amersham Biosciences). Nonspecific sites were blocked by incubation of the membrane in blocking buffer [5% nonfat dry milk in T-TBS (TBS containing 0.05% Tween 20)] overnight. The membranes were incubated with the indicated primary antibodies [Bax (1: 1000, Abcam), cleaved poly (ADP-ribose) polymerase (PARP) (1:1000, Cell Signaling), caspase 3 (1: 1000, Cell Signaling), Bcl-2 (1:200, Abcam), (ICAM)-1 (1: 2000, Abcam), polyclonal antibodies against tumor necrotic factor (TNF)-α (1: 1000, Cell Signaling), nuclear factor (NF)-κB (1: 250, Abcam), MMP-9 (1:3000, Abcam), CXCR4 (1:1000, Abcam), stromal cell-derived factor (SDF)-1α (1:1000, Cell Signaling), NAD(P)H quinone oxidoreductase (NQO) 1 (1: 1000, Abcam), heme oxygense (HO)-1 (1: 250, Abcam), NADPH oxidase (NOX)-1 (1:1500, Sigma), NOX-2 (1:500, Sigma), cytosolic cytochrome C (1:2000, BD), mitochondrial cytochrome C (1:2000, BD), and GLP-1R (1:1000, abcam)] for 1 hour at room temperature. Horseradish peroxidase-conjugated anti-rabbit immunoglobulin IgG (1:2000, Cell Signaling) was used as a secondary antibody for one-hour incubation at room temperature. The washing procedure was repeated eight times within one hour. Immunoreactive bands were visualized by enhanced chemiluminescence (ECL; Amersham Biosciences) and exposed to Biomax L film (Kodak). For the purpose of quantification, ECL signals were digitized using Labwork software (UVP).
Oxidative stress reaction in LV myocardium
The procedure and protocol for assessing the protein expression of oxidative stress have been described in details in our previous reports ,. The Oxyblot Oxidized Protein Detection Kit was purchased from Chemicon (S7150). DNPH derivatization was carried out on 6 μg of protein for 15 minutes according to the manufacturer’s instructions. One-dimensional electrophoresis was carried out on 12% SDS/polyacrylamide gel after DNPH derivatization. Proteins were transferred to nitrocellulose membranes which were then incubated in the primary antibody solution (anti-DNP 1: 150) for 2 hours, followed by incubation in secondary antibody solution (1:300) for 1 hour at room temperature. The washing procedure was repeated eight times within 40 minutes. Immunoreactive bands were visualized by enhanced chemiluminescence (ECL; Amersham Biosciences) which was then exposed to Biomax L film (Kodak). For quantification, ECL signals were digitized using Labwork software (UVP). For oxyblot protein analysis, a standard control was loaded on each gel.
Immunofluorescent (IF) and immunohistochemical (IHC) staining
IF staining was performed for the examinations of CD68+ and γ-H2AX cells in LV myocardium using respective primary antibodies based on our recent study ,,. Moreover, IHC staining was performed for examinations of CD14 and CD40 using respective primary antibodies as described ,,. Irrelevant antibodies were used as controls in the current study.
Histological quantification of myocardial fibrosis/infarct and collagen deposition
The procedure and protocol was described in details in our previous report . Briefly, hematoxylin and eosin (H&E) and Masson's trichrome staining were used for identifying the infarct area and fibrosis of LV myocardium, respectively. Three serial sections of LV myocardium in each animal at the same levels were prepared at 4 μm thickness by Cryostat (Leica CM3050S). The integrated area (μm2) of infarct area and fibrosis on each section were calculated using the Image Tool 3 (IT3) image analysis software (University of Texas, Health Science Center, San Antonio, UTHSCSA; Image Tool for Windows, Version 3.0, USA). Three randomly selected high-power fields (HPFs) (100 ×) were analyzed in each section. After determining the number of pixels in each infarct and fibrotic area per HPF, the numbers of pixels obtained from three HPFs were summated. The procedure was repeated in two other section for each animal. The mean pixel number per HPF for each animal was then determined by summating all pixel numbers and dividing by 9. The mean integrated area (μm2) of fibrosis in LV myocardium per HPF was obtained using a conversion factor of 19.24 (1 μm2 represented 19.24 pixels).
To analyze the extent of collagen synthesis and deposition, cardiac paraffin sections (6 μm) were stained with picrosirius red (1% Sirius red in saturated picric acid solution) for one hour at room temperature using standard methods. The sections were then washed twice with 0.5% acetic acid. The water was physically removed from the slides by vigorous shaking. After dehydration in 100% ethanol thrice, the sections were cleaned with xylene and mounted in a resinous medium. High power fields (×100) of each section were used to identify Sirius red-positive area on each section. Analytical sections of collagen deposition area in LV myocardium were identical to the description for the calculations of the infarct and fibrotic areas.
Quantitative data are expressed as means ± SD. Statistical analysis was adequately performed by ANOVA followed by Bonferroni multiple-comparison post hoc test. SAS statistical software for Windows version 8.2 (SAS institute, Cary, NC) was utilized. A probability value <0.05 was considered statistically significant.
The circulating level of GLP-1 at 72 h after IR injury
The circulating level of glycogen-like-peptide (GLP)-1 and echocardiography findings in five study groups of animals
Group 1 (n = 8)
Group 2 (n = 8)
Group 4 (n = 8)
Group 3 (n = 8)
Group 5 (n = 8)
Serum GLP-1 level (pg/ml)*
32.6 ± 2.3a
39.1 ± 3.1b
42.1 ± 4.7b,c
45.2 ± 2.9c
48.2 ± 4.1d,c
6.8 ± 0.21
6.7 ± 0.21
6.4 ± 0.23
6.5 ± 0.24
6.5 ± 0.30
3.4 ± 0.20
3.5 ± 0.18
3.4 ± 0.21
3.5 ± 0.20
3.4 ± 0.22
79.0 ± 1.8
79.0 ± 2.10
76.2 ± 3.70
77.0 ± 2.30
78.1 ± 2.80
Day 3 echocardiography*
6.5 ± 0.24a
6.9 ± 0.37b
6.4 ± 0.38a
6.8 ± 0.34b
6.7 ± 0.28b
3.3 ± 0.18a
5.7 ± 0.24b
3.4 ± 0.22a
4.3 ± 0.27c
4.2 ± 0.21c
81.0 ± 1.60a
34.0 ± 4.2b
78.0 ± 3.40a
67.0 ± 3.70c
67 ± 3.30c
Heart function prior to and at 72 h after IR injury
Table 1 showed the results of echocardiography findings. Prior to the IR procedure (i.e. day 0), the left ventricular ejection fraction (LVEF), left ventricular end-diastolic dimension (LVEDd) and left ventricular end-systolic dimension (LVESd) did not differ among the five groups. However, at 72 h after reperfusion, LVEF was significantly reduced, whereas LVEDd and LVESd were significantly increased in the WT-IR group as compared with the other groups. Additionally, LVEF was significantly reduced whereas LVEDd and LVESd were significantly increased in WT-IR-Sita and DPP4D-IR groups as compared to those of WT-SC and DPP4D-SC groups, but is showed no significant difference in these three parameters between the former two groups or between the latter two groups at 72 h after reperfusion. These findings suggest that DPP4D and sitagliptin treatment preserved LV function and inhibited LV remodeling in the setting of IR-induced myocardial damage.
ROS generation and histopathological findings at 72 h after IR procedure
Identifications of DNA damage marker and inflammatory cells in infarct region using IHC and IF stains at 72 h after reperfusion
Protein expressions of inflammatory biomarkers at 72 h after reperfusion
Myocardial ROS production, and protein expressions of ROS and oxidative stress at 72 h after reperfusion
Protein expressions of apoptosis, anti-apoptosis, and mitochondrial damage biomarkers at 72 h after reperfusion
The protein expressions of GLP-1R and anti-oxidants at 72 h after IR procedure
The expressions of angiogenesis factors and cardiac stem cells at 72 h after IR procedure
This study, which utilized DPP4-deficiency rats to clarify the therapeutic impact of sitagliptin, an oral hypoglycemic agent with distinctive property of inhibiting DPP4 enzyme activity, on the heart against IR injury in a rodent model, yielded several striking implications. First, not only were the size of LV infarct area and collagen deposition in infarct area significantly reduced, but LV function was also notably preserved in the WT-IR-Sita group than that in the WT-IR group. Second, the expressions of inflammatory, oxidative-stress, ROS, apoptotic, and myocardial damage biomarkers in infarct myocardium were remarkably reduced in the WT-IR-Sita animals than those in the WT-IR group. Consistently, the pattern of changes in these parameters in the DPP4D-IR group was identical to that in the WT-IR-Sita group. Third, the circulating GLP-1 levels and the expressions of anti-oxidants and GLP-1R in infarct myocardium were found to be markedly higher in the WT-IR-Sita group than that in the WT-IR group. In this regard, the changes of these biomarkers in DPP4D-IR animals showed a similar pattern compared to that in their WT-IR-Sita counterparts.
Mechanisms underlying reduction of infarct size, suppression of LV remodeling, and preservation of LV function after sitagliptin treatment ― role of inhibiting DPP4 enzyme activity
Although several previous studies have shown that DPP4 inhibitors are capable of offering cardiovascular protection and preserving cardiac functions from myocardial ischemia ,,-, the precise mechanisms involved have not been extensively investigated. The most important findings in the present study is that, as compared with WT-SC, the infarct size, the fibrotic zone and collagen-deposited area of infarct myocardium and LV remodeling were substantially increased, whereas the cardiac function was notably reduced in the WT-IR animals and were remarkably restored in the WT-IR-Sita animals. To further elucidate whether the observation of cardiac protection offered by sitagliptin was through the inhibition of DPP4 enzyme activity, the extent of IR injury in DPP4-deficiency rats was investigated. As expected, the cardiac protective effects (i.e., reduction of infarct size, fibrotic area collagen-deposited region, and LV remodeling as well as preservation of cardiac function) in DPP4D-IR animals were found to be identical to that in the WT-IR-Sita group. Our results are consistent with those of previous studies , that demonstrated cardiac protection against ischemia-related myocardial injury through genetic deletion of DPP4.
Up-regulating down-stream signalings of inflammatory reaction and the generations of oxidative stress and ROS in ischemia-reperfusion injury ― role of GLP-1 receptor pathway
Our previous experimental ,,, have clearly shown that inflammation, ROS (i.e., oxygen free radicals), and oxidative stress, which are deleterious contributors to mitochondrial damage and cellular apoptosis, fibrosis and death as well as the propagation of organ dysfunction, were markedly up-regulated in the setting of ischemic organ dysfunction. The findings are consistent with those of the present study that demonstrated significant up-regulations in inflammation, ROS and oxidative stress, as well as apoptosis in the WT-IR animals compared with those in the WT-SC and DPP4D-SC animals. One distinctive finding is that these parameters were substantially down-regulated and the anti-apoptotic markers were notably up-regulated in the WT-IR-Sita animals. This is also in concert with the finding of our recent study that demonstrated remarkable inhibition of the expressions of inflammation, ROS, and oxidative stress in the settings of acute kidney injury and critical limb ischemia after sitagliptin treatment ,. Another intriguing finding is that there was no difference in these parameters between the WT-IR-Sita and DPP4D-IR animals. Therefore, the findings suggest that sitagliptin suppressed inflammatory reaction, oxidative stress (i.e., the generations of ROS), and cellular apoptosis through the up-regulation of circulating GLP-1 and the interaction between GLP-1 and GLP-1R (i.e., GLP-1R pathway) on cardiomyocytes in the setting of cardiac IR injury. Accordingly, our findings also strengthen those of previous studies that demonstrated cardiovascular protective effect of DPP4 inhibitor/DPP4-deficiency through attenuating the productions of ROS  and oxidative stress .
Inhibiting damaging effect of ROS and oxidative stress on myocardium through GLP-1-GLP-1R interacting pathway ― Up-regulation of anti-oxidant production
Anti-oxidants have been fully accepted as scavengers of ROS that alleviate oxidative stress at molecular-cellular level, especially in ischemia-related organ damage. Our recent study has shown that both sitagliptin and extendin-4 (i.e., an analogs of GLP-1) treatment offered effective cytoprotection through up-regulating the production of anti-oxidants and reducing the tissue levels of ROS in acute kidney IR injury . A principal finding in the present study is that the protein expressions of antioxidants (HO-1, NQO 1) was markedly higher in WT-IR and DDF4D-SC animals than in WT-SC animals and the levels of these biomarkers were further markedly elevated in the WT-IR-Sita and the DPP4D-IR animals. The findings of high-level anti-oxidant production in DPP4D-IR animals imply that sitagliptin offers cardioprotective effect via enhancing the generation of anti-oxidants that alleviate the deleterious effect of ROS/oxidative stress on cardiomyocytes.
Enhanced angiogenesis in infarct myocardium ― role of sitagliptin and deletion of DPP4 enzyme activity
A previous study has demonstrated that inhibition of DPP4 activity by enalapril enhanced the mobilization of endothelial progenitor cell (EPC) from bone marrow to circulation in the setting of critical limb ischemia . Similarly, our recent studies have revealed that sitagliptin therapy augmented EPC mobilization from bone marrow to circulation and enhanced angiogenesis in ischemic regions ,. An important finding in the current study is that, as compared with WT-SC and DPP4D-SC animals, the protein expression of angiogenesis factors (i.e., CXCR4 and SDF-1α) and the number of cardiac stem cells (i.e., c-kit and Sca-1) in infarct area were significantly higher in WT-IR animals. These findings may suggest that the ischemic stimulus triggered an intrinsic response in tissue/organ for self-protection. Intriguingly, these biomarkers were found to be notably higher in WT-IR-Sita than in WT-IR group. These findings corroborate those of our recent studies ,. Of importance is that the expressions of these biomarkers in infarct LV did not differ between the WT-IR-Sita and DPP4D-IR animals. Our findings, in addition to supporting those of previous studies , also highlight that enhancement of angiogenesis and cardiac stem cell in ischemic area is mainly through the abrogating DPP4 activity. Therefore, our findings suggest that sitagliptin therapy and deletion of DPP4 may offer benefit in preserving cardiac function through restoring blood flow and regeneration of lost myocardium by cardiac stem cells.
This study has limitations. First, this study did not investigate the impact of inhibition of DPP4 activity on long-term outcome of the animals after IR procedure. Second, although the dosage of sitagliptin to be utilized was based on our previous report , this study did not investigate which was the optimal sitagliptin dosage for the best myocardial protecting in the present IR setting based on pilot experiments.
In conclusion, inhibition of DPP4 activity protected the heart against IR injury and left ventricular remodeling and preserved heart function through down-regulating inflammation, oxidative stress, ROS generation, and cell apoptosis as well as up-regulating antioxidant production and angiogenesis.
This study was supported by a program grant from Chang Gung Memorial Hospital, Chang Gung University (Grant number: CMRPG8B0551).
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