Simvastatin Treatment Protects Myocardium in Noncoronary Artery Cardiac Surgery by Inhibiting Apoptosis Through miR-15a-5p Targeting

被引:15
|
作者
Zhou, Li [1 ,2 ]
Liu, Xiang [1 ,2 ,3 ]
Wang, Zhen-Qing [1 ,2 ,3 ]
Li, Yan [1 ,2 ,3 ]
Shi, Mao-Mao [1 ,2 ,3 ]
Xu, Zhe [1 ,2 ]
Ou, Zhi-Jun [2 ,3 ,4 ]
Li, Hua-Ming [1 ,2 ,3 ]
Cheng, Tian-Pu [1 ,2 ,3 ]
Jian, Yu-Peng [1 ,2 ,3 ]
Zhang, Wen [1 ,2 ]
Liu, Chen [2 ,3 ,5 ]
Zhang, Xi [1 ,2 ]
Quon, Michael J. [6 ]
Zhang, Chun-Xiang [7 ]
Xu, Ying-Qi [1 ,2 ]
Wang, Zhi-Ping [1 ,2 ]
Ou, Jing-Song [1 ,2 ,3 ,8 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 1, Heart Ctr, Div Cardiac Surg, 58 Zhong Shan Er Rd, Guangzhou 510080, Guangdong, Peoples R China
[2] Minist Hlth, Key Lab Assisted Circulat, Guangzhou, Guangdong, Peoples R China
[3] Natl & Guangdong Prov Joint Engn Lab Diag & Treat, Guangzhou, Guangdong, Peoples R China
[4] Sun Yat sen Univ, Heart Ctr, Div Hypertens & Vasc Dis, Affiliated Hosp 1, Guangzhou, Guangdong, Peoples R China
[5] Sun Yat Sen Univ, Heart Ctr, Dept Cardiol, Affiliated Hosp 1, Guangzhou, Guangdong, Peoples R China
[6] Univ Maryland, Sch Med, Div Endocrinol Diabet & Nutr, Baltimore, MD 21201 USA
[7] Univ Alabama Birmingham, Dept Biomed Engn, Sch Med, Birmingham, AL 35294 USA
[8] Guangdong Prov Key Lab Brain Funct & Dis, Guangzhou, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
simvastatin; cardiomyocyte; apoptosis; cardiac surgery; microRNA; NITRIC-OXIDE SYNTHASE; IMPAIRS ENDOTHELIAL FUNCTION; PLACEBO-CONTROLLED TRIAL; HIGH-RISK PATIENTS; STATIN THERAPY; CARDIOPLEGIC ARREST; BYPASS-SURGERY; ATRIAL-FIBRILLATION; DOWN-REGULATION; INDUCED INJURY;
D O I
10.1097/FJC.0000000000000611
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Simvastatin treatment is cardioprotective in patients undergoing noncoronary artery cardiac surgery. However, the mechanisms by which simvastatin treatment protects the myocardium under these conditions are not fully understood. Seventy patients undergoing noncoronary cardiac surgery, 35 from a simvastatin treatment group and 35 from a control treatment group, were enrolled in our clinical study. Simvastatin (20 mg/d) was administered preoperatively for 5-7 days. Myocardial tissue biopsies were taken before and after surgery. Apoptosis was detected by TUNEL staining. The expressions of Bcl-2 and Bak in myocardial tissue were detected by immunoblotting. The expressions of miRNA and Bcl-2 mRNA were detected by quantitative real-time polymerase chain reaction assays. Cardiomyocytes were isolated from rat and cultured cells. MiR-15a-5p mimic was transfected into cardiomyocytes, and the Bcl-2 was detected by immunoblotting. TUNEL staining showed significantly less myocardial apoptosis in the simvastatin treatment group when compared with the control treatment group. Protein expression of Bcl-2 was increased in the simvastatin treatment group before surgery, and Bak expression was increased in the control treatment group after surgery. Further comparisons showed that Bcl-2/Bak ratios were reduced in the control treatment group but were not significantly changed in the simvastatin treatment group after surgery. Furthermore, microarray assays revealed that miR-15a-5p was significantly decreased by simvastatin treatment. This was validated by quantitative real-time polymerase chain reaction analysis. MiR-15a-5p was predicted to target Bcl-2 mRNA at nucleotide positions 2529-2536. This was validated by luciferase binding assays. Coincident with the change in miR-15a-5p, the mRNA expression of Bcl-2 was increased in the simvastatin treatment group. MiR-15a-5p mimic significantly inhibited Bcl-2 expression in cardiomyocytes. Our findings strongly suggest that simvastatin treatment preoperatively protected the myocardium in patients undergoing noncoronary artery cardiac surgery, at least in part, by inhibiting apoptosis via suppressing miR-15a-5p expression, leading to increasing expression of Bcl-2 and decreasing expression of Bak.
引用
收藏
页码:176 / 185
页数:10
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