Table 3.
Research Model | Model establishment | Intervention methods | Drug effects | Main molecular mechanisms | Citation |
---|---|---|---|---|---|
Male SD rats with MIR | Ligating LAD to induce ischemia for 30 min, followed by 4 h of reperfusion | 50 mg/kg intraperitoneal injection at 0.5 h before the induction of ischemia | Cardioprotection, suppressing inflammation, suppressing oxidative stress |
⬇ cTnI, CK-MB, LVEDP, MDA, TNF-α, IL-6, IL-8, p-p38, p38 ⬆ LVSP, SOD, CAT, GPx |
[16] |
HR primary porcine cardiomyocytes | Hypoxia 2 h, reoxygenation 3 h | 20 μg/ml for 4 h (validation concentration) | Reducing apoptosis, anti-inflammation, reducing mitochondrial injury |
⬇ Bax, cleaved caspase-3, Cyt-c, TNF-α, IL-6, ROS, HIF-1α, ET-1, TGF-β ⬆ Bcl-2, eNOS, PGC1-α |
[33] |
Wistar rats with MI | Ligating LAD | 1.2, 1.8, and 3.6 mg/kg, intraperitoneally daily for 3 weeks | Cardioprotection, improving cardiac function |
⬇Infarct area, CK, LDH, myocardial apoptosis, LVID, Bax ⬆ LVAWd/s, EF, FS, SV, Bcl-2 |
[35] |
Male SD rats with myocardial ischemia | Injection of ISO (85 mg/kg/day) for 2 consecutive days | 1.2, 1.8, and 3.6 mg/kg, intraperitoneally daily for 1 week | Reducing oxidative stress damage, reducing cardiomyocyte apoptosis |
⬇ Myocardial fibrosis, inflammatory cell infiltration, MDA, p-iNOS, iNOS, Cyt-c, caspase-3, caspase-9 ⬆ SOD, CAT, GSH-Px, eNOS, Bcl-2, Bax, JNK, p-JNK |
[36] |
Male SD rats with MI | Ligating LAD | 7 and 14 mg/kg intraperitoneal injection for 1 week | Cardioprotection, improving cardiac function, regulating coronary artery vasodilation |
⬇ cTnT, LDH, myocardial infarction area, LVID, Ca2+ release by the ryanodine receptor, SR Ca2+ leakage ⬆ H2S in serum and myocardial tissue, LVAWd/s, EF, FS, SV, CSE, CBS, opening of KATP, Ca2+ transients amplitude, Ca2+ uptake via SERCA, Ca2+ removal via the NCX, myofilament sensitivity, SR Ca2+content |
[57] |
Male Wistar rats with MIR | Ligating LAD to induce ischemia for 30 min, followed by 3 h of reperfusion | 1.88 mg/kg, orally via gavage, 12 h before inducing ischemia | Anti-apoptosis, improving cardiac function |
⬇ LVIDd/s, infarct size, Bax, cleaved caspase-3, cleaved caspase-9, GRK2, p-GRK2, p-CaMKII, p-PLC-γ, p-IP3R ⬆ LVAWd/s, LVEF, Bcl-2, PI3K, p-PI3K |
[58] |
Male C57BL6 mice with MIR | Ligating LAD to induce ischemia for 30 min, followed by 3 h of reperfusion | 3 mg/ml 10 min + 5 mg/ml 15 min (intravenously) before MIR | Promoting angiogenesis, improving cardiac function |
⬇ LVID, cardiac fibrosis areas, miR-19a-3p ⬆ EF, FS, LVAWd/s, neovascularization numbers, LDH, COX-2, p-AKT, p-PI3K, p-mTOR, VEGF, MMP-2 |
[59] |
CaMKII Ca2+/Calmodulin-dependent protein kinase II, CBS cystathionine beta-synthase, CK creatine kinase, COX-2 cyclooxygenase-2, CSE cystathionine-γ-lyase, cTnT cardiac troponin T, Cyt-c cytosolic cytochrome C, EF ejection fraction, ET-1 endothelin-1, FS short-axis shortening, GPx glutathione peroxidase, JNK c-Jun N-terminal kinase, LVAWd/s left ventricular anterior wall diastolic and systolic thicknesses, MDA malondialdehyde, MIR myocardial ischemia reperfusion, MMP-2 matrix metalloproteinas-2, NCX Na+/Ca2+ exchanger, p-mTOR p-mammalian target of rapamycin, PLC-γ recombinant phospholipase C gamma, p-PI3K p-phosphatidylinositol-3-kinase, iNOS inducible nitric oxide synthase, SV stroke volume, SD Sprague Dawley, SERCA sarco/endoplasmic reticulum Ca2+-ATPase, SR sarcoplasmic reticulum, TGF-β transforming growth factor-β, VLDL very low-density lipoprotein cholesterol, VEGF vascular endothelial growth factor