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表没食子儿茶素-3-没食子酸酯对兔快速心房起搏模型心房电重构和结构重构的保护作用

Protective effects of epigallocatechin-3 gallate on atrial electrical and structural remodeling in a rabbit rapid atrial pacing model.

作者信息

Zhu Jifa, Zhang Xiao, Li Ling, Su Gang

机构信息

Department of Cardiology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, China,

出版信息

Cell Biochem Biophys. 2015 Mar;71(2):897-903. doi: 10.1007/s12013-014-0280-2.

Abstract

Epigallocatechin-3 gallate (EGCG) is the major catechin in green tea. The aim of this study is to investigate the effects of EGCG on atrial electrical and structural remodeling in a rabbit rapid atrial pacing (RAP) model. New Zealand white rabbits were subjected to RAP with or without EGCG treatment. The atrial electrophysiology was studied. ELISA, Western blots, and RT-PCR were performed to determine the level of the inflammation markers, oxidative stress, and fibrogenic agents. Atrial tissue was stained with Masson's trichrome stain for fibrosis detection. RAP rabbits showed a significantly shorter atrial effective refractory period than control rabbits. Higher AF inducibility and longer AF duration were seen in the RAP group. AERP of rabbits received high dose EGCG were prolonged compared to RAP rabbits, and AF inducibility and duration of rabbits received high dose EGCG were lower. RAP rabbits have higher inflammation markers, higher oxidative stress, and more significant fibrosis within atrium, while high dose intervention of EGCG can lower the inflammation, oxidative stress, and fibrosis induced by RAP. Results showed that EGCG have protective effects on atrial electrical and structural remodeling in a rabbit RAP model in terms of attenuating of inflammation and oxidative stress.

摘要

表没食子儿茶素-3-没食子酸酯(EGCG)是绿茶中的主要儿茶素。本研究旨在探讨EGCG对兔快速心房起搏(RAP)模型中心房电重构和结构重构的影响。将新西兰白兔分为接受或未接受EGCG治疗的RAP组。研究心房电生理学。采用酶联免疫吸附测定(ELISA)、蛋白质免疫印迹法(Western blots)和逆转录聚合酶链反应(RT-PCR)来测定炎症标志物、氧化应激和纤维化因子的水平。用马松三色染色法对心房组织进行染色以检测纤维化。RAP兔的心房有效不应期明显短于对照兔。RAP组的房颤诱发率更高,房颤持续时间更长。与RAP兔相比,接受高剂量EGCG的兔的心房有效不应期延长,接受高剂量EGCG的兔的房颤诱发率和持续时间更低。RAP兔心房内炎症标志物水平更高、氧化应激更强、纤维化更明显,而高剂量EGCG干预可降低RAP诱导的炎症、氧化应激和纤维化。结果表明,EGCG在减轻炎症和氧化应激方面对兔RAP模型中的心房电重构和结构重构具有保护作用。

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