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二十二碳六烯酸介导MAPK途径抗房颤的作用及机制研究
引用本文:徐庆梅,莫辰,朱飞宇,张恒,王洪巨,高琴,康品方,唐碧.二十二碳六烯酸介导MAPK途径抗房颤的作用及机制研究[J].蚌埠医学院学报,2021,46(1):1-5.
作者姓名:徐庆梅  莫辰  朱飞宇  张恒  王洪巨  高琴  康品方  唐碧
作者单位:1.蚌埠医学院第一附属医院 心血管科, 安徽 蚌埠 2330042.蚌埠医学院 生理学教研室, 安徽 蚌埠 2330303.蚌埠医学院 心脑血管研究中心, 安徽 蚌埠 233030
基金项目:安徽省教育厅重大项目;国家自然科学基金面上项目;安徽省自然科学基金青年项目;蚌埠医学院研究生科研创新计划
摘    要:目的:探讨二十二碳六烯酸(DHA)通过影响P38 MAPK途径调控胶原表达发挥抗房颤作用可能的机制.方法:将80只对乙酰胆碱(66μg/mL)-氯化钙(50 mg/mL)混合液敏感的SD大鼠随机分为对照组(CON组)、对照DHA处理组(DHA组)、房颤组(AF组)和房颤DHA处理组(DHA+AF组),每组20只复制大鼠...

关 键 词:心房颤动  心房纤维化  二十二碳六烯酸  细胞外基质  MAPK途径
收稿时间:2020-03-01

Study on the effects and mechanism of MAPK pathway mediated by docosahexaenoic acid against atrial fibrillation
XU Qing-mei,MO Chen,ZHU Fei-yu,ZHANG Heng,WANG Hong-ju,GAO Qin,KANG Pin-fang,TANG Bi.Study on the effects and mechanism of MAPK pathway mediated by docosahexaenoic acid against atrial fibrillation[J].Journal of Bengbu Medical College,2021,46(1):1-5.
Authors:XU Qing-mei  MO Chen  ZHU Fei-yu  ZHANG Heng  WANG Hong-ju  GAO Qin  KANG Pin-fang  TANG Bi
Affiliation:1.Department of Cardiovascular Medicine, The First Affiliated Hospital of Bengbu Medical College, Bengbu Anhui 2330042.Department of Physiology, Bengbu Medical College, Bengbu Anhui 233030, China3.Center for Cardiovascular and Cerebrovascular Research, Bengbu Medical College, Bengbu Anhui 233030, China
Abstract:ObjectiveTo investigate the possible mechanism of docosahexaenoic acid(DHA) regulating collagen expression by affecting the P38 MAPK pathway to play an anti-atrial fibrillation.MethodsEighty SD rats sensitive to acetylcholine(66 μg/mL)-calcium chloride(50 mg/mL) mixture were randomly divided into the control group(CON group), control DHA treatment group(DHA group), atrial fibrillation group(AF group) and atrial fibrillation DHA treatment group(DHA+AF group)(20 rats in each group model of atrial fibrillation).The BL-420F tractive electrocardiogram and continuous double stimulation method were used to detect the atrial effective refractory period(ERP), the whole cell patch clamp technique was used to record the atrial muscle cell action potential duration(APD) change, the enzyme immunosorbent assay(ELISA) was used to detect the typeⅠ, Ⅲ collagen expression in atrial muscle tissue of rats, and the expression levels of P38 and P-PP38 and MKP 1 protein were detected using Western blotting.ResultsThe duration of atrial fibrillation in rats prolonged with the increasing of experimental time, while DHA could shorten the duration of atrial fibrillation(P < 0.05 to P < 0.01).The ERP and APD significantly shortened, while DHA could significantly prolong the atrial ERP and APD in AF group(P < 0.01).There was no significant change in P38 protein among each group.Compared with the CON group, the expression level of P-P38 significantly increased, while the expression level of MKP-1 decreased in AF group(P < 0.01). Compared with the AF group, the expression level of P-P38 significantly decreased, while the expression level of MKP-1 increased in the DHA+AF group(P < 0.01).The results of ELISA showed that DHA could obviously down-regulate the typeⅠand Ⅲ collagen expression(P < 0.01).ConclusionsDHA may play an anti-atrial fibrillation role by regulating P38 MAPK signal transduction pathway mediating collagen expression.
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