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丹红注射液对大鼠慢性应激反应中心肌酶和HSP70表达的影响(PDF)

《心脏杂志》[ISSN:1009-7236/CN:61-1268/R]

期数:
2017年第2期
页码:
154-157,163
栏目:
基础研究
出版日期:
2016-11-25

文章信息/Info

Title:
Effect of danhong injection on myocardial enzymes and expression of heat shock protein 70 in chronic stress reaction in rats
作者:
王 凯1宮惠琳1叶季鲜2邵丽杰2谢学建2杨 晶23
(1.西安交通大学第一附属医院病理科,陕西 西安 710061;
2.解放军第323医院心血管内科,陕西 西安 710054;
3.西安医学院研究生院,陕西 西安 710021)
Author(s):
WANG Kai1 GONG Hui-lin1 YE Ji-xian2 SHAO Li-jie2 XIE Xue-jian2 YANG Jing23
(1.Department of Pathology, First Affiliated Hospital, Medical College, Xi’an Jiaotong University, Xi’an 710061, Shaanxi, China;
2.Department of Cardiology, PLA 323 Hospital, Xi’an 710054, Shaanxi, China;
3.Graduate School, Xi’an Medical University, Xi’an 710021, Shaanxi, China)
关键词:
丹红注射液慢性应激心肌酶 热休克蛋白70
Keywords:
danhong injection chronic stress myocardial enzyme heat shock protein 70
分类号:
R544
DOI:
-
文献标识码:
A
摘要:
目的 通过心肌酶和热休克蛋白(HSP)70的表达来观察慢性应激反应中丹红注射液对大鼠心肌的保护作用。方法 将健康成年SD大鼠55只随机分为空白对照组、丹红对照组、慢性应激组和慢性应激丹红组。空白对照组不进行慢性应激处理,也不注射丹红注射液;丹红对照组不进行慢性应激处理,仅每日经腹腔注射丹红注射液10 ml/kg;慢性应激组按照慢性应激反应模型进行处理;慢性应激丹红组在按照慢性应激反应模型进行处理的同时每日经腹腔注射丹红注射液10 ml/kg。待慢性应激持续到设定时间时(3周),剖杀4组大鼠,① 观察各组大鼠心肌酶的变化。②同时采用免疫组织化学法检测各组大鼠心肌组织中HSP70的表达情况。结果 ①与空白对照组比较,丹红对照组、慢性应激组和慢性应激丹红组大鼠乳酸脱氢酶(LDH)和肌酸激酶同工酶 (CK-MB)显著升高(P<0.01)。慢性应激组LDH和CK-MB较丹红对照组显著升高(P<0.05),慢性应激丹红组LDH和CK-MB较慢性应激组显著降低(P<0.05);而丹红对照组和慢性应激丹红组之间无显著性差异。②丹红对照组、慢性应激组和慢性应激丹红组心肌组织HSP70表达均强于空白对照组。丹红对照组和慢性应激组之间HSP70表达无显著性差异。慢性应激丹红组心肌组织HSP70表达强于丹红对照组或慢性应激组。结论 丹红注射液的使用可有效抑制慢性应激大鼠LDH、CK-MB的升高,还可增高慢性应激大鼠心肌组织中HSP70的表达。
Abstract:
AIM To investigate the myocardial protective effect of danhong injection in chronic stress reaction of rats by observing myocardial enzyme and expression of heat shock protein 70 (HSP70). METHODS Fifty-five healthy adult Sprague Dawley rats were randomly divided into blank control group, danhong injection control group, chronic stress group, and chronic stress danhong injection group. The blank control group was treated with neither chronic stress nor danhong injection. The danhong injection control group was treated with intraperitoneal injection of danhong (daily 10 ml/kg) but not the chronic stress group. The chronic stress group was treated according to the chronic stress model processing and the chronic stress danhong injection group was treated in accordance with the treatment of chronic stress reaction model and intraperitoneal injection of danhong injection (daily, 10 ml/kg). After 3-week chronic stress, rats in the four groups were killed, changes of myocardial enzyme were observed, and expression of HSP70 in myocardial tissue was detected using immunohistochemical method. RESULTS Compared with those in the blank control group, lactate dehydrogenase (LDH) and creatine kinase isoenzyme (CK-MB) in the danhong injection control group, chronic stress group, and chronic stress danhong injection group significantly increased (P<0.01). LDH and CK-MB in the chronic stress group increased significantly compared with those in the danhong injection control group (P<0.05) and LDH and CK-MB in the chronic stress danhong injection group decreased significantly compared with those in the chronic stress group (P<0.05). But no significant difference was found between the danhong injection control group and the chronic stress danhong injection group. Expression of HSP70 of myocardial tissue in the danhong injection control group, chronic stress group, and the chronic stress danhong injection group were stronger than that in the blank control group. There was no significant difference between the danhong injection control group and the chronic stress group. However, the expression of HSP70 in the chronic stress danhong injection group was stronger than that in the danhong injection control group and the chronic stress group. CONCLUSION Danhong injection effectively inhibited the increase of LDH and CK-MB in chronic stress rats and increased the expression of HSP70 in myocardial tissue of chronic stress rats.

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备注/Memo

备注/Memo:
收稿日期:2016-05-04.
基金项目:兰州军区医药卫生科技攻关项目资助(CLZ13JB19);解放军第323医院重大培育课题资助(2012323A02)
通讯作者:杨晶,副主任医师,主要从事心血管内科临床及离子通道基础研究 Email:yangjing323@163.com
作者简介:王凯,助理研究员,硕士 Email:gbwangkai@163.com
更新日期/Last Update: 2016-10-11