Ethanol inhibition of Ca2+ and Na+ currents in the guinea-pig heart

Yoshizumi Habuchi, Taiji Furukawa, Hideo Tanaka, Ling-Ling Lu, Junichiro Morikawa, Manabu Yoshimura
{"title":"Ethanol inhibition of Ca2+ and Na+ currents in the guinea-pig heart","authors":"Yoshizumi Habuchi,&nbsp;Taiji Furukawa,&nbsp;Hideo Tanaka,&nbsp;Ling-Ling Lu,&nbsp;Junichiro Morikawa,&nbsp;Manabu Yoshimura","doi":"10.1016/0926-6917(95)90006-3","DOIUrl":null,"url":null,"abstract":"<div><p>The effects of ethanol on L-type Ca<sup>2+</sup> and fast Na<sup>+</sup> currents (<em>I</em><sub>Ca</sub>, and <em>I</em><sub>Na</sub>, respectively) were examined using the whole-cell patch-clamp experiments on guinea-pig ventricular cells. At a clinically relevant concentration of 24 mM, ethanol slightly but significantly shortened the action potential duration, and reduced the <em>I</em><sub>Ca</sub> by 7 ± 4% (mean ± S.D.). This concentration of ethanol did not affect <em>I</em><sub>Na</sub>, but a lethal concentration of ethanol (80 mM) significantly inhibited <em>I</em><sub>Na</sub> by 13 ± 5%. The voltage dependence of <em>I</em><sub>Na</sub> activation was not affected by ethanol, whereas the inhibitions of <em>I</em><sub>Ca</sub> by 80 mM ethanol and <em>I</em><sub>Na</sub> by 240 mM were both accompanied by a several mV shift in the channel availability curve toward more negative potentials, suggesting that the channels in the inactivated state are more susceptible to ethanol. The <em>I</em><sub>Ca</sub> inhibition by ethanol at clinically relevant concentrations could contribute to a negative inotropic effect, action potential shortening and development of arrhythmias, while the pathophysiological significance of ethanol inhibition of <em>I</em><sub>Na</sub> seems less important.</p></div>","PeriodicalId":100501,"journal":{"name":"European Journal of Pharmacology: Environmental Toxicology and Pharmacology","volume":"292 2","pages":"Pages 143-149"},"PeriodicalIF":0.0000,"publicationDate":"1995-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0926-6917(95)90006-3","citationCount":"54","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Pharmacology: Environmental Toxicology and Pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0926691795900063","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 54

Abstract

The effects of ethanol on L-type Ca2+ and fast Na+ currents (ICa, and INa, respectively) were examined using the whole-cell patch-clamp experiments on guinea-pig ventricular cells. At a clinically relevant concentration of 24 mM, ethanol slightly but significantly shortened the action potential duration, and reduced the ICa by 7 ± 4% (mean ± S.D.). This concentration of ethanol did not affect INa, but a lethal concentration of ethanol (80 mM) significantly inhibited INa by 13 ± 5%. The voltage dependence of INa activation was not affected by ethanol, whereas the inhibitions of ICa by 80 mM ethanol and INa by 240 mM were both accompanied by a several mV shift in the channel availability curve toward more negative potentials, suggesting that the channels in the inactivated state are more susceptible to ethanol. The ICa inhibition by ethanol at clinically relevant concentrations could contribute to a negative inotropic effect, action potential shortening and development of arrhythmias, while the pathophysiological significance of ethanol inhibition of INa seems less important.

乙醇对豚鼠心脏Ca2+和Na+电流的抑制作用
采用全细胞膜片钳实验对豚鼠心室细胞进行了乙醇对l型Ca2+和快速Na+电流(分别为ICa和INa)的影响。在临床相关浓度为24 mM时,乙醇可轻微但显著缩短动作电位持续时间,使ICa降低7±4%(平均±sd)。该浓度的乙醇不影响INa,但致死浓度的乙醇(80 mM)显著抑制INa(13±5%)。乙醇对INa激活的电压依赖性不受影响,而80 mM乙醇对ICa和240 mM乙醇对INa的抑制作用都伴随着通道可用性曲线向负电位方向移动数mV,表明失活状态的通道更容易受到乙醇的影响。在临床相关浓度下,乙醇对ICa的抑制可能导致负性肌力作用、动作电位缩短和心律失常的发生,而乙醇对INa的抑制的病理生理意义似乎不太重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信