温阳通脉方通过JAK2/STAT3信号通路保护大鼠心肌缺血再灌注损伤  

Wenyang Tongmai decoction protects myocardial ischemia-reperfusion injury in rats via JAK2/STAT3 pathway

作　　者：李媛媛 张恒 王笑 石月萍 LI Yuanyuan;ZHANG Heng;WANG Xiao;SHI Yueping(Department of Traditional Chinese Medicine,the First Affiliated Hospital of Jinzhou Medical University,Jinzhou,Liaoning121000,Chirm)

机构地区：[1]锦州医科大学附属第一医院中医科

出　　处：《中国动脉硬化杂志》2019年第6期468-474,共7页Chinese Journal of Arteriosclerosis

基　　金：辽宁省科学技术基金资助项目(201602307)

摘　　要：目的探讨温阳通脉方是否通过Janus蛋白酪氨酸激酶2(JAK2)/信号转导和转录激活因子3(STAT3)信号转导通路,调节水通道蛋白(AQP)的表达,发挥对缺血再灌注心肌组织的保护作用。方法将30只雄性SD大鼠随机分为5组,每组6只:假手术组、模型组及温阳通脉方低剂量治疗组、中剂量治疗组和高剂量治疗组。将大鼠灌胃给药14天后,结扎心脏左冠状动脉前降支,按缺血30min再灌注120min的方法建立心肌缺血再灌注损伤模型。全自动生化分析仪检测各组大鼠的血清肌酸激酶同工酶(CK-MB)、乳酸脱氢酶(LDH);心电图检测大鼠ST段抬高情况;HE染色观察心脏组织病理形态学变化;免疫组织化学染色检测心肌组织中AQP1、AQP4蛋白的表达;Westernblot检测JAK2、p-JAK2、STAT3、p-STAT3、AQP1、AQP4的蛋白表达。结果与假手术组比较,模型组大鼠血清中的CK-MB、LDH含量显著上升(P<0.01),缺血30min与再灌注120min后心电图的ST段显著抬高(P<0.01),HE染色显示模型组的心肌细胞损伤严重,AQP1、AQP4免疫组织化学表达明显增多(P<0.01),JAK2、p-JAK2、STAT3、p-STAT3、AQP1、AQP4的蛋白表达均明显升高(P<0.01)。与模型组相比,给药大鼠CK-MB、LDH水平明显降低(P<0.01),缺血30min与再灌注120min后的ST段均降低(P<0.01),心肌细胞损伤均可见不同程度减轻,AQP1、AQP4免疫组织化学表达明显减少,JAK2、p-JAK2、STAT3、p-STAT3整体的表达呈升高趋势,尤其是p-JAK2和p-STAT3的表达(P<0.01),AQP1、AQP4的水平均有不同程度降低(P<0.01)。结论温阳通脉方的心肌保护作用可能与激活JAK2/STAT3信号通路,下调AQP1和AQP4的表达有关。Aim To explore whether Wenyang Tongmai decoction can regulate JAK2/STAT3 signal transduction pathway and the expression of aquaporins(AQP) to protect myocardial ischemia-reperfusion tissue.Methods Thirty male SD rats were randomly divided into 5 groups,6 in each group:sham operation group,ischemia-reperfusion group,low-dose treatment group,middle-dose treatment group,high-dose treatment group.After 14 days of intragastric administration,the model of myocardial ischemia-reperfusion injury was established by ligation of the left anterior descending coronary artery for 30 minutes and then releasing the ligated artery for 120 minutes.The serum levels of creatine kinase isoenzymes (CK-MB) and lactate dehydrogenase (LDH) were detected by automatic biochemical analyzer.The ST-segment elevation of the rats was counted in the electrocardiogram.Pathological changes in cardiac tissue were observed by HE staining.The expressions of AQP1 and AQP4 in myocardial tissue were detected by immunohistochemical staining.The protein expressions of JAK2,p-JAK2,STAT3,p-STAT3,AQP1 and AQP4 were detected by Western blot method.Results Compared with the sham group,the levels of CK-MB and LDH in the serum of the ischemia-reperfusion group were significantly increased (P<0.01),and the ST-segments of the electrocardiogram were significantly elevated after ischemia for 30 minutes and reperfusion for 120 minutes(P<0.01).HE staining showed that the myocardial cells in the ischemia-reperfusion group were severely damaged.The expressions of AQP1 and AQP4 in immunohistochemistry was significantly increased (P<0.01).The results of Western blot showed that the expressions of JAK2,p-JAK2,STAT3,p-STAT3,AQP1 and AQP4 were significantly increased (P<0.01).Compared with the ischemia-reperfusion group,the serum levels of CK-MB and LDH were significantly decreased in the treated rats (P<0.01),and the ST-segments were decreased after 30 minutes ischemia and 120 minutes reperfusion (P<0.01),myocardial cells’ damage was alleviated to varying degrees in HE st

关 键 词：温阳通脉方 心肌缺血再灌注损伤 JAK2/STAT3信号通路 水通道蛋白1 水通道蛋白4 

分 类 号：R256.22[医药卫生—中医内科学] R5[医药卫生—中医学]