Simvastatin Alleviates Myocardial Contractile Dysfunction and Lethal Ischemic Injury in Rat Heart Independent of Cholesterol-Lowering Effects

被引:41
作者
Adameova, A. [2 ]
Harcarova, A. [2 ]
Matejikova, J. [2 ]
Pancza, D. [1 ]
Kuzelova, M. [2 ]
Carnicka, S. [1 ]
Svec, P. [2 ]
Bartekova, M. [1 ]
Styk, J. [1 ]
Ravingerova, T. [1 ]
机构
[1] Slovak Acad Sci, Heart Res Inst, Ctr Excellence Cardiovasc Res, POB 104,Dubravska Cesta 9, Bratislava 84005, Slovakia
[2] Comenius Univ, Fac Pharm, Dept Pharmacol & Toxicol, Bratislava, Slovakia
关键词
Statins; Cholesterol; Pleiotropic effects; Heart; Ischemia; INFARCT SIZE; REPERFUSION INJURY; ATORVASTATIN; ROSUVASTATIN; REDUCTION; HYPERCHOLESTEROLEMIA; ISCHEMIA/REPERFUSION; ARRHYTHMIAS; ACTIVATION; CONTRIBUTE;
D O I
10.33549/physiolres.931751
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Statins, the inhibitors of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase, are most frequently used drugs in the prevention of coronary artery disease due to their cholesterol-lowering activity. However, it is not exactly known whether these effects of statins or those independent of cholesterol decrease account for the protection against myocardial ischemia-reperfusion (I/R) injury. In this study, we investigated the effect of 5-day treatment with simvastatin (10 mg/kg) in Langendorffperfused hearts of healthy control (C) and diabetic-hypercholesterolemic (D-H; streptozotocin + high fat-cholesterol diet, 5 days) rats subjected to 30-min global ischemia followed by 40-min reperfusion for the examination of postischemic contractile dysfunction and reperfusion-induced ventricular arrhythmias or to 30-min (left anterior descending) coronary artery occlusion and 2-h reperfusion for the infarct size determination (IS; tetrazolium staining). Postischemic recovery of left ventricular developed pressure (LVDP) in animals with D-H was improved by simvastatin therapy (62.7 +/- 18.2 % of preischemic values vs. 30.3 +/- 5.7 % in the untreated D-H; P<0.05), similar to the values in the simvastatin-treated C group, which were 2.5-fold higher than those in the untreated C group. No ventricular fibrillation occurred in the simvastatin-treated C and D-H animals during reperfusion. Likewise, simvastatin shortened the duration of ventricular tachycardia (10.2 +/- 8.1 s and 57.8 +/- 29.3 s in C and D-H vs. 143.6 +/- 28.6 s and 159.3 +/- 44.3 s in untreated C and D-H, respectively, both P<0.05). The decreased arrhythmogenesis in the simvastatin-treated groups correlated with the limitation of IS (in % of risk area) by 66 % and 62 % in C and D-H groups, respectively. However, simvastatin treatment decreased plasma cholesterol levels neither in the D-H animals nor in C. The results indicate that other effects of statins (independent of cholesterol lowering) are involved in the improvement of contractile recovery and attenuation of lethal I/R injury in both, healthy and diseased individuals.
引用
收藏
页码:449 / 452
页数:4
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