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熊果酸减轻糖尿病大鼠心脏缺血再灌注损伤

简磊 高明杰 夏旋

天然产物研究与开发2017,Vol.29Issue(5):843-848,6.
天然产物研究与开发2017,Vol.29Issue(5):843-848,6.DOI:10.16333/j.1001-6880.2017.5.022

熊果酸减轻糖尿病大鼠心脏缺血再灌注损伤

Ursolic Acid Attenuate Myocardial Ischemia Reperfusion Injury in Diabetic Rats

简磊 1高明杰 1夏旋1

作者信息

  • 1. 三峡大学仁和医院内分泌科,宜昌443000
  • 折叠

摘要

Abstract

To explore the effect and potential mechanism of ursolic acid(UA) in myocardial ischemia reperfusion injury (MI/R) of diabetic rats.The model of diabetic rats were induced by injecting Streptozotocin and observed for 2 weeks.Diabetic rats were randomly divided into Sham group (Sham),myocardial ischemia reperfusion injury group (MI/R),and ursolic acid(low,middle,high) pretreatment group (UA).The MI/R model was induced by ligating left anterior descending coronary artery of diabetic rats.The cardial Systolic and diastolic function,the cardial infarct size and the expression of acute cardiac injury biomarkers (CK-MB,AST and LDH),AKT,p-AKT,PI3K,IL-6,IL-1β,TNF-α,BCL-2 and TUNEL were examined in the rats of all groups.Compared with the Sham group,MI/R group had higher infarct size and the expression of CK,AST,LDH,p-AKT,PI3 K,IL-6,IL-1β,TNF-α,Bax and TUNEL and with lower expression of BCL-2 and the cardial Systolic and diastolic function.Compared with the MI/R group,the UA group had lower expression of infarct size and the expression of CK,AST,LDH,p-AKT,PI3 K,IL-6,IL-1β,TNF-α,Bax and TUNEL with higher cardial Systolic and diastolic function and BCL-2 expression.There was no difference on the expression of AKT among three groups.UA pretreatment can protect diabetic rats against myocardial ischemia reperfusion injury by attenuating inflammation and apoptosis.The mechanism of which was associaing with suppressing the activation of AKT/PI3K signal pathway.

关键词

熊果酸/心脏缺血再灌注损伤/炎症/凋亡

Key words

ursolic acid/myocardial ischemia reperfusion injury/inflammation/apoptosis

分类

医药卫生

引用本文复制引用

简磊,高明杰,夏旋..熊果酸减轻糖尿病大鼠心脏缺血再灌注损伤[J].天然产物研究与开发,2017,29(5):843-848,6.

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