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内质网应激在大鼠缺血再灌注损伤心肌中的表达▲
Express of endoplasmic reticulum stress in rat myocardium with ischemiareperfusion injury

微创医学 201712卷03期 页码:306-308+311

作者机构:(广西医科大学第一附属医院心胸外科,南宁市530021)

基金信息:▲基金项目:广西自然科学基金(编号:2013GXNSFAA019152),广西壮族自治区卫生厅课题(编号:Z2012108) *通信作者

DOI:DOI:10.11864/j.issn.1673.2017.03.02

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  • 英文简介
  • 参考文献
【摘要】目的探讨内质网应激(ERS)在大鼠缺血再灌注损伤心肌中的表达以及小剂量衣霉素(TM)预处理对缺血再灌注损伤心肌的影响。方法SD大鼠30只随机分为三组,假手术组(Sham组)、缺血再灌注组(IR组)、衣霉素处理+IR组(TM+IR组),每组10只。Sham组单纯开胸,不结扎冠状动脉;IR组开胸,结扎前降支30 min,再灌注2 h;TM+IR组TM腹腔注射0.6 mg/kg,30 min后结扎前降支30 min,再灌注2 h。于开胸后,心肌再灌注2 h抽血,检测肌钙蛋白I(cTnI)含量,透射电镜观察再灌注2 h心肌的超微结构,检测再灌注2 h心肌的GRP78 mRNA及蛋白表达。结果IR组和TM+IR组在再灌注2 h时,cTnI水平均明显上升;IR组心肌超微结构损伤最严重,TM+IR组次之。再灌注2 h后,GRP78 mRNA及蛋白,IR组及TM+IR组明显升高。结论MIRI可诱导ERS,小剂量TM预处理可减轻MIRI。
【Abstract】 ObjectiveTo explore the expression of endoplasmic reticulum stress (ERS) in rat myocardium with ischemiareperfusion injury and the effect of preconditioning with smalldose tunicamycin on myocardium with ischemiareperfusion injury. MethodsThirty SD rats were randomly divided into 3 groups including shamoperation group (Sham group), ischemiareperfusion injury group (IR group) and tunicamycin + ischemiareperfusion injury ( TM+IR group),ten rats in each group. Simple thoracotomy without coronary artery ligation was performed in the Sham group.Thoracotomy and twohour reperfusion after 30 minutes of the anterior descending coronary artery ligation were performed in the IR group. In the IR+TM group, ligation of the anterior descending coronary artery for 30 minutes was performed after 30 minutes of intraperitoneal injection with tunicamycin (0.6ml/kg), then twohour reperfusion was conducted. The content of cardiac troponin I (cTnI) was detected after thoracotomy and after 2 hours of cardiac reperfusion. The myocardial ultrastructure was observed under transmission electron microscope and the expressions of myocardial glucose regulated protein 78 (GRP78) mRNA and protein were detected after 2 hours of reperfusion. ResultsThe cTnI levels were significantly increased in the IR group and TM + IR group at 2 hours after reperfusion. The damage of myocardial ultrastructure was the most severe in the IR group , and was the second severe in the TM+IR group. GRP78 mRNA and protein expressions increased significantly in the IR group and TM+IR group at 2 hours after reperfusion. ConclusionMyocardial ischemiareperfusion injury (MIRI) may induce ERS. And preconditioning with smalldose tunicamycin may alleviate MIRI.

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