Adameova A, Harcarova A, Matejikova J, Pancza D, Kuzelova M, Carnicka S, Svec P, Bartekova M, Styk J, Ravingerova T
1Department of Pharmacology and Toxicology, Facultyof Pharmacy Comenius University, Bratislava, Slovak Republic.
Physiol Res. 2009;58(3):449-454. doi: 10.33549/physiolres.931751.
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 Langendorff-perfused 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.
他汀类药物是3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶的抑制剂,因其降胆固醇活性而成为预防冠状动脉疾病最常用的药物。然而,目前尚不清楚他汀类药物的这些作用是通过降低胆固醇,还是通过与降低胆固醇无关的其他作用来预防心肌缺血再灌注(I/R)损伤。在本研究中,我们研究了辛伐他汀(10 mg/kg)连续5天治疗对健康对照(C)组和糖尿病高胆固醇血症(D-H组;链脲佐菌素+高脂高胆固醇饮食,5天)组大鼠Langendorff灌注心脏的影响。两组大鼠均先经历30分钟全心缺血,随后40分钟再灌注,以检测缺血后收缩功能障碍和再灌注诱导的室性心律失常;或经历30分钟(左冠状动脉前降支)冠状动脉闭塞和2小时再灌注,以测定梗死面积(IS;四氮唑染色)。辛伐他汀治疗改善了D-H组动物缺血后左心室舒张末压(LVDP)的恢复(缺血前值的62.7±18.2%,而未治疗的D-H组为30.3±5.7%;P<0.05),与辛伐他汀治疗的C组相似,后者比未治疗的C组高2.5倍。辛伐他汀治疗的C组和D-H组动物在再灌注期间均未发生心室颤动。同样,辛伐他汀缩短了室性心动过速的持续时间(C组和D-H组分别为10.2±8.1秒和57.8±29.3秒,而未治疗的C组和D-H组分别为143.6±28.6秒和159.3±44.3秒,均P<0.05)。辛伐他汀治疗组心律失常发生率的降低与梗死面积(占危险区的百分比)的减小相关,C组和D-H组分别降低了66%和62%。然而,辛伐他汀治疗既未降低D-H组动物的血浆胆固醇水平,也未降低C组动物的血浆胆固醇水平。结果表明,他汀类药物的其他作用(与降低胆固醇无关)参与了健康个体和患病个体收缩功能恢复的改善以及致死性I/R损伤的减轻。