Effects of Acute and Chronic Atorvastatin on Cardioprotection of Ischemic Postconditioning in Isolated Rat Hearts

被引:18
作者
Fan, Ying [1 ]
Yang, Shusen [1 ]
Cao, Yang [1 ]
Huang, Yonglin [1 ]
机构
[1] Harbin Med Univ, Affiliated Hosp 1, Dept Cardiol, Harbin, Heilongjiang, Peoples R China
关键词
Atorvastatin; Ischemia-reperfusion injury; Ischemic postconditioning; Isolated heart; ACTIVATED PROTEIN-KINASE; NITRIC-OXIDE SYNTHASE; INFARCT SIZE; REPERFUSION INJURY; MYOCARDIAL-INFARCTION; CHOLESTEROL; PATHWAY; SIMVASTATIN; LIMITATION;
D O I
10.1111/j.1755-5922.2012.00318.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Myocardial reperfusion therapy remains the most effective strategy to limit infarct size and improve clinical outcome. However, reperfusion injury is still inevitable, and a number of strategies have been developed to ameliorate its lethal outcome. The beneficial roles of ischemic postconditioning (Ipost) have regained more interest in targeting myocardial reperfusion phase to improve cardioprotection. Aims This study was to determine whether acute or chronic treatment with atorvastatin affects cardioprotection when it was combined with Ipost. Results Acute or chronic atorvastatin treatment significantly reduced infarct size and recovered contractile dysfunction during reperfusion. When Ipost was combined with atorvastatin treatment, chronic, but not acute, atorvastatin therapy attenuated the cardioprotective effects of Ipost. Chronic, but not acute, atorvastatin treatment also abolished Ipost-induced phosphorylation level of Akt and endothelial nitric oxide synthase (eNOS). Conclusions Chronic atorvastatin treatment could interfere with cardioprotective effects of Ipost on limiting infarct size and contractile dysfunction, possibly via inhibition of Akt and eNOS activity. This study suggests that Ipost should be used carefully when atorvastatin is taken by patients with AMI.
引用
收藏
页码:187 / 192
页数:6
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