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培养的金鱼促性腺激素细胞的电膜特性和离子电流

Electrical membrane properties and ionic currents in cultured goldfish gonadotrophs.

作者信息

Van Goor F, Goldberg J I, Chang J P

机构信息

Department of Biological Sciences, University of Alberta, Edmonton, Canada.

出版信息

Can J Physiol Pharmacol. 1996 Jun;74(6):729-43.

PMID:8909786
Abstract

The electrical membrane properties and ionic currents of cultured identified goldfish gonadotrophs were characterized using whole-cell patch-clamp recordings. Under current-clamp recording conditions, goldfish gonadotrophs had a resting membrane potential of approximately -60 mV and an input resistance of 8.2 +/- 1.6 G omega. In response to depolarizing current injections, one or more action potentials could be induced from resting membrane potential or more hyperpolarized holding potentials. In addition, some cells exhibited spontaneous action potential activity. Under voltage-clamp recording conditions, several outward and inward currents were isolated and characterized using pharmacological and ionic substitution studies. The outward currents included a fast-activating, transient current and an inactivation-resistant current similar to IA-type and delayed rectifier currents, respectively. Unlike mammalian gonadotrophs, apamin-sensitive K+ currents were not detected. Inward currents included a fast-activating and inactivating Na+ current and a high-voltage activated, dihydropyridine-sensitive Ca2+ current. The value for half-maximal steady-state inactivation of the Na+ and Ca2+ currents was -50.8 and -16.7 mV, respectively, indicating that a significant proportion of both Na+ and Ca2+ channels are available for activation at the resting membrane potential of these cells.

摘要

利用全细胞膜片钳记录技术对培养的已鉴定金鱼促性腺激素细胞的电膜特性和离子电流进行了表征。在电流钳记录条件下,金鱼促性腺激素细胞的静息膜电位约为 -60 mV,输入电阻为8.2±1.6 GΩ。响应去极化电流注入,可从静息膜电位或更超极化的钳制电位诱导出一个或多个动作电位。此外,一些细胞表现出自发动作电位活动。在电压钳记录条件下,利用药理学和离子替代研究分离并表征了几种外向和内向电流。外向电流包括一个快速激活的瞬时电流和一个类似于IA型电流和延迟整流电流的抗失活电流。与哺乳动物促性腺激素细胞不同,未检测到蜂毒明肽敏感的K+电流。内向电流包括一个快速激活和失活的Na+电流以及一个高电压激活的、对二氢吡啶敏感的Ca2+电流。Na+和Ca2+电流的半数最大稳态失活值分别为 -50.8和 -16.7 mV,这表明在这些细胞的静息膜电位下,相当一部分Na+和Ca2+通道可用于激活。

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