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褪黑素减轻心肌缺血/再灌注损伤的作用及机制

《心脏杂志》[ISSN:1009-7236/CN:61-1268/R]

期数:
2015年第3期
页码:
255-259,270
栏目:
基础研究
出版日期:
2015-01-11

文章信息/Info

Title:
Protective effect of melatonin treatment against myocardial ischemia/reperfusion injury
作者:
于立明1杨 阳1刘丽君2裴海峰3金振晓1段维勋1俞世强1
(第四军医大学西京医院:1.心血管外科,3.心血管内科,陕西 西安 710032;
2.西北大学生命科学学院,陕西 西安 710000)
Author(s):
YU Li-ming1 YANG Yang1 LIU Li-jun2 PEI Hai-feng3 JIN Zhen-xiao1 DUAN Wei-xun1 YU Shi-qiang1
(1.Department of Cardiovascular Surgery, 3.Department of Cardiology, Xijing Hospital, Fourth Military Medical University, Xi’an 710032, Shaanxi, China;
2.College of Life Science, Northwest University, Xi’an 710000, Shaanxi, China)
关键词:
褪黑素心肌缺血再灌注损伤沉默信息转录调控因子1心肌保护凋亡
Keywords:
melatonin myocardial ischemia/reperfusion injury silent information regulator of transcription 1 cardioprotection apoptosis
分类号:
Q57
DOI:
-
文献标识码:
A
摘要:
目的:探讨褪黑素(melatonin,Mel)在大鼠心肌缺血/再灌注(MI/R)损伤中的拮抗作用及其机制。方法:80只体质量200~250 g雄性SD大鼠随机分为4组:假手术(Sham)组、溶剂对照(MI/R+V)组、Mel治疗(MI/R+Mel)组、Mel+EX527(MI/R+Mel+EX)组。常规结扎左冠状动脉前降支行心肌缺血/再灌注手术,缺血30 min,再灌72 h后超声心动图法检测各组大鼠心功能,再灌6 h后ELISA法检测血清酶学指标,TUNEL法检测心肌细胞凋亡率,Evans blue-TTC双染法测定梗死面积,Western blot法检测沉默信息转录调控因子1(SIRT1)、乙酰化叉头转录因子1(Ac-Foxo1)及凋亡相关蛋白表达水平。结果:Mel治疗可显著改善MI/R损伤后心功能,降低血清肌酸激酶(CK)及乳酸脱氢酶(LDH)水平,降低凋亡率及梗死面积,上调SIRT1表达,下调Ac-Foxo1水平,降低凋亡相关蛋白表达。而使用EX527阻断SIRT1信号后逆转Mel的上述作用(均P<0.01)。结论:Mel可发挥抗凋亡作用减轻MI/R损伤并改善心功能,其作用机制可能与其激活SIRT1信号通路并降低Ac-Foxo1水平有关。
Abstract:
AIM:To investigate the protective effect of melatonin (Mel) on myocardial ischemia/reperfusion (MI/R) injury and its underlying mechanisms. METHODS: Eighty male Sprague Dawley rats (200-250 g) were subjected to myocardial ischemia/reperfusion (MI/R, I 30 min, R 6 h) and randomly divided into four groups: MI/R+V (absolute alcohol diluted in sterile saline to 0.1 M, 1 ml/d, 7 d before MI/R; 1 ml/d, 15 min before reperfusion, ip), MI/R+Mel [(10 mg/(kg·d), 7 d before MI/R; 15 mg/(kg·d), 15 min before reperfusion], MI/R+Mel+EX [Mel treatment following the same routine; EX527, 5 mg/(kg·d), every other day for three times; 5 mg/(kg·d), 20 min before reperfusion] and sham (rats undergoing the same surgical procedures without tying the suture). Cardiac function 72 h after reperfusion, serum CK and LDH level, apoptotic index, infarct size, SIRT1 expression, Ac-Foxo1 expression and apoptosis related protein expression was detected. RESULTS: Seventy two h after MI/R operation, melatonin treatment group showed improved cardiac function, lower serum CK and LDH levels, decreased apoptotic index, decreased infarct size, upregulated SIRT1 expression, downregulated Ac-Foxo1 expression and decreased apoptosis related protein expression (all P<0.01). Moreover, SIRT1 inhibitor EX527 downregulated SIRT1 expression, upregulated Ac-Foxo1 expression and blocked the cardioprotective effect of melatonin. CONCLUSION: These data indicate that melatonin treatment attenuates myocardial ischemia/reperfusion injury by reducing apoptosis via a SIRT1 dependent signaling pathway.

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备注/Memo

备注/Memo:
收稿日期:2014-07-11.
基金项目:国家十二五学科支撑计划项目资助(2011BAI11B20);国家自然科学基金项目资助(81102687和81070198);陕西省社会发展计划项目资助(2012JQ4001);西京医院学科助推计划项目资助(XJZT09M16和XJZT10M11)
通讯作者:俞世强,主任医师,主要从事微创心脏外科研究Email:shiqiangyu210@126.com
共同通讯作者:段维勋,主治医师,主要从事抗心肌缺血/再灌注损伤的基础研究Email:duanweixun@126.com
作者简介:于立明,博士生Email:lmyu2012@163.com
更新日期/Last Update: 2015-02-03