上海大学学报(自然科学版) ›› 2018, Vol. 24 ›› Issue (6): 853-860.doi: 10.12066/j.issn.1007-2861.2096

• 研究论文 •    下一篇

Sigma-1 受体激活减轻心脏缺血再灌注损伤

廖小平1, 喻溥蛟2, 许嘉鸿2()   

  1. 1.上海市安亭医院 心血管内科, 上海 201805
    2.同济大学附属同济医院 心血管内科, 上海 200065
  • 收稿日期:2018-06-22 出版日期:2018-12-30 发布日期:2018-12-24
  • 通讯作者: 许嘉鸿 E-mail:xujiahong@tongji.edu.cn
  • 基金资助:
    国家自然科学基金面上资助项目(81670362);国家自然科学基金面上资助项目(81470515);嘉定区科委卫生系统科研资助项目(2014-KW-02)

Effectiveness of activation of sigma-1 receptor on reducing myocardium injury in ischemia reperfusion

LIAO Xiaoping1, YU Pujiao2, XU Jiahong2()   

  1. 1. Department of Cardiology, Anting Hospital, Shanghai 201805, China
    2. Department of Cardiology, Tongji Hospital Affiliated to Tongji University, Shanghai 200065, China
  • Received:2018-06-22 Online:2018-12-30 Published:2018-12-24
  • Contact: XU Jiahong E-mail:xujiahong@tongji.edu.cn

摘要:

[目的] 研究 sigma-1 受体的激活与抑制对心脏缺血再灌注损伤的作用. [方法] C57BL/6 小鼠经过 3 d 尾静脉注射 sigma-1 受体抑制剂 BD1047, sigma-1 受体激动剂 SA4503 或生理盐水后施行心脏缺血再灌注手术. 术后对小鼠心脏进行 TTC/Evans 蓝双染色并计算心脏梗死区 (infarction area, INF) 与危险区 (area at risk, AAR) 比值(INF/AAR), 同时对心肌组织采用蛋白免疫印迹法检测凋亡相关蛋白 Bcl-2, Bax, Caspase-3 的表达水平. [结果] 接受了 sigma-1 受体抑制剂 BD1047 预处理的小鼠, 其 INF/AAR 值远大于对照组 ($P\!<$0.05), 心肌组织中促凋亡相关蛋白的表达水平升高, 抗凋亡相关蛋白的表达水平降低. 而接受 sigma-1 受体激动剂 SA4503 预处理的小鼠, 其 INF/AAR 值远小于对照组 ($P\!<$0.05), 心肌组织中促凋亡相关蛋白的表达水平降低, 抗凋亡相关蛋白的表达水平升高. [结论] Sigma-1 受体的激活能够改善心脏缺血再灌注损伤, 而抑制 sigma-1 受体则会加重心脏缺血再灌注损伤.

关键词: Sigma-1受体, 心肌梗死, 缺血再灌注损伤

Abstract:

[Objective] This paper attempts to investigate whether sigma-1 receptor (Sig1R) activation attenuate myocardial ischemia reperfusion injury (MIRI) and whether Sig1R inhibition exacerbates MIRI in mice model. [Methods] C57BL/6 mice are injected via tail vein with BD1047 (Sig1R inhibitor), SA4503 (Sig1R activator) or saline 3 days before MIRI surgery. Then, double-staining technique and western blot analysis are performed on myocardium tissue. [Results] Mice that have received BD1047 pretreatment demonstrate a significant increase in the myocardial infarction size after I/R compared with control group ($P\!\!<$0.05), and a significantly increased expression of Bax and Caspases-3 proteins and a significantly reduced expression of Bcl-2 protein compared with sham control, MIRI control and sham BD1047 groups ($P\!<$0.05). Mice that have received SA4503 pretreatment demonstrate a significant reduction in myocardial infarction size after I/R compared with control group ($P\!<$0.05), and a significantly reduced expression of Bax and cleaved Caspases-3 proteins and a significantly increased expression of Bcl-2 protein compared with sham control, MIRI control and sham SA4503 groups ($P\!<$0.05). [Conclusions] SA4503 protects MIRI and reduces myocardial infarction whereas BD1047 deteriorates MIRI and augment myocardial infarction, and these effects may be achieved through activation or inhibition of Sig1R.

Key words: Sigma-1 receptor, mycardial infarction, ischemia reperfusion injury

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