Literature DB >> 29985281

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

Li Zhou1,2, Xiang Liu1,2,3, Zhen-Qing Wang1,2,3, Yan Li1,2,3, Mao-Mao Shi1,2,3, Zhe Xu1,2, Zhi-Jun Ou2,3,4, Hua-Ming Li1,2,3, Tian-Pu Cheng1,2,3, Yu-Peng Jian1,2,3, Wen Zhang1,2, Chen Liu2,3,5, Xi Zhang1,2, Michael J Quon6, Chun-Xiang Zhang7, Ying-Qi Xu1,2, Zhi-Ping Wang1,2, Jing-Song Ou1,2,3,8.   

Abstract

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.

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Year:  2018        PMID: 29985281     DOI: 10.1097/FJC.0000000000000611

Source DB:  PubMed          Journal:  J Cardiovasc Pharmacol        ISSN: 0160-2446            Impact factor:   3.105


  7 in total

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Authors:  Yinghao Wang; Shuisheng Wu; Ce Yang; Hanyun Gao; Hongmin Yu; Xuehua Lu; Shugang Yuan
Journal:  Front Pharmacol       Date:  2019-10-17       Impact factor: 5.810

Review 2.  Programmed Cell Death: Complex Regulatory Networks in Cardiovascular Disease.

Authors:  Liuhua Zhou; Jiateng Sun; Lingfeng Gu; Sibo Wang; Tongtong Yang; Tianwen Wei; Tiankai Shan; Hao Wang; Liansheng Wang
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3.  TMAO-Activated Hepatocyte-Derived Exosomes Are Widely Distributed in Mice with Different Patterns and Promote Vascular Inflammation.

Authors:  Xiang Liu; Jiazichao Tu; Ziqin Zhou; Bingxin Huang; Jianrong Zhou; Jimei Chen
Journal:  Cardiol Res Pract       Date:  2022-02-14       Impact factor: 1.866

4.  TMAO-Activated Hepatocyte-Derived Exosomes Impair Angiogenesis via Repressing CXCR4.

Authors:  Xiang Liu; Yijia Shao; Jiazichao Tu; Jiapan Sun; Bing Dong; Zhichao Wang; Jianrong Zhou; Long Chen; Jun Tao; Jimei Chen
Journal:  Front Cell Dev Biol       Date:  2022-01-31

5.  Trimethylamine-N-oxide-stimulated hepatocyte-derived exosomes promote inflammation and endothelial dysfunction through nuclear factor-kappa B signaling.

Authors:  Xiang Liu; Yijia Shao; Jiazichao Tu; Jiapan Sun; Lifu Li; Jun Tao; Jimei Chen
Journal:  Ann Transl Med       Date:  2021-11

6.  MiR-19b-3p regulated by BC002059/ABHD10 axis promotes cell apoptosis in myocardial infarction.

Authors:  Bihong Liao; Shaohong Dong; Zhenglei Xu; Fei Gao; Suihao Zhang; Ruijuan Liang
Journal:  Biol Direct       Date:  2022-08-18       Impact factor: 7.173

Review 7.  The Emerging Role of Noncoding RNA Regulation of the Ferroptosis in Cardiovascular Diseases.

Authors:  Jing Zhang; Xinran Liu; Xiaozhong Li; Yuxi Cai; Yiwen Zhou; Qiong Wang; Zhou Xu; Panpan Xia; Pingping Yang; Lei Jun; Peng Yu; Ao Shi
Journal:  Oxid Med Cell Longev       Date:  2022-09-21       Impact factor: 7.310

  7 in total

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