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白藜芦醇对哇巴因诱导的豚鼠乳头肌延迟后除极和触发活动的影响。

Effects of resveratrol on delayed afterdepolarization and triggered activity induced by ouabain in guinea pig papillary muscles.

作者信息

Zhang Li-Ping, Ma Hui-Jie, Zhao Juan, Wang Qing-Shan

机构信息

Department of Physiology, Institute of Basic Medicine, Hebei Medical University, Shijiazhuang 050017, China.

出版信息

Sheng Li Xue Bao. 2005 Jun 25;57(3):361-6.

Abstract

The purpose of this study was to investigate the effects of resveratrol on delayed afterdepolarization (DAD) and triggered activity (TA) induced by ouabain in guinea pig papillary muscles and the underlying mechanism. Action potentials were recorded using intracellular microelectrode technique. The results obtained are as follows: (1) DAD and TA induced by ouabain (1 micromol/L) were inhibited by pretreatment with resveratrol (30, 60, and 120 micromol/L) in a concentration-dependent manner; (2) Pretreatment with N(G)-nitro-L-arginine methyl ester (L-NAME, 1 mmol/L), a nitric oxide (NO) synthase inhibitor, failed to abolish the above effect of resveratrol (60 micromol/L ); (3) 5 micromol/L 17beta-estradiol (E(2)) or 30 micromol/L resveratrol had no effects on DAD and TA, however, resveratrol combined with E(2) at the same doses exerted significant inhibitory effects on DAD and TA; (4) Pretreatment with tamoxifen (TAM, 10 micromol/L), an inhibitor of estrogen receptor, also did not blocked the effects of resveratrol (60 micromol/L) on DAD and TA induced by ouabain. All these results indicated that resveratrol exerted an inhibitory effects on DAD and TA induced by ouabain, possibly by reducing calcium influx, which might not be mediated by NO and estrogen receptor. The antiarrhythmic effects of resveratrol may contribute to its cardioprotective action.

摘要

本研究旨在探讨白藜芦醇对哇巴因诱导的豚鼠乳头肌延迟后除极(DAD)和触发活动(TA)的影响及其潜在机制。采用细胞内微电极技术记录动作电位。结果如下:(1)白藜芦醇(30、60和120 μmol/L)预处理可浓度依赖性地抑制哇巴因(1 μmol/L)诱导的DAD和TA;(2)一氧化氮(NO)合酶抑制剂N(G)-硝基-L-精氨酸甲酯(L-NAME,1 mmol/L)预处理未能消除白藜芦醇(60 μmol/L)的上述作用;(3)5 μmol/L 17β-雌二醇(E2)或30 μmol/L白藜芦醇对DAD和TA无影响,然而,相同剂量的白藜芦醇与E2联合应用对DAD和TA具有显著抑制作用;(4)雌激素受体抑制剂他莫昔芬(TAM,10 μmol/L)预处理也未阻断白藜芦醇(60 μmol/L)对哇巴因诱导的DAD和TA的作用。所有这些结果表明,白藜芦醇对哇巴因诱导的DAD和TA具有抑制作用,可能是通过减少钙内流实现的,这可能不是由NO和雌激素受体介导的。白藜芦醇的抗心律失常作用可能有助于其心脏保护作用。

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