Suppr超能文献

一种在肾上腺皮质细胞中受促肾上腺皮质激素和血管紧张素II抑制的新型钾离子电流。

A novel K+ current inhibited by adrenocorticotropic hormone and angiotensin II in adrenal cortical cells.

作者信息

Mlinar B, Biagi B A, Enyeart J J

机构信息

Department of Pharmacology, Ohio State University, College of Medicine, Columbus 43210-1239.

出版信息

J Biol Chem. 1993 Apr 25;268(12):8640-4.

PMID:8386167
Abstract

Adrenocorticotropic hormone (ACTH) and angiotensin II (AII) are peptides that regulate the production of steroid hormones by cells of the adrenal cortex. The cellular mechanisms linking these peptides to corticosteroid hormone secretion are not understood. In patch clamp recordings from bovine adrenal zona fasciculata (AZF) cells, we have identified a novel cholera toxin-sensitive K+ current (IAC), which is potently inhibited by both ACTH and AII with respective EC50 values of 4.5 and 145 pM. These two peptides depolarize AZF cells with a temporal pattern and potency that parallels the inhibition of IAC. With the discovery of IAC, we have identified a common molecular target for both ACTH and AII. The convergent inhibition of IAC by these two peptides suggests a mechanism whereby biochemical signals originating at the cell membrane can be transduced to depolarization-dependent Ca2+ entry and steroid hormone secretion.

摘要

促肾上腺皮质激素(ACTH)和血管紧张素II(AII)是调节肾上腺皮质细胞甾体激素生成的肽类物质。目前尚不清楚将这些肽类与皮质类固醇激素分泌联系起来的细胞机制。在对牛肾上腺束状带(AZF)细胞进行的膜片钳记录中,我们发现了一种新型的霍乱毒素敏感钾电流(IAC),ACTH和AII均可有效抑制该电流,其半数有效浓度(EC50)分别为4.5和145 pM。这两种肽以一种与IAC抑制作用平行的时间模式和效力使AZF细胞去极化。随着IAC的发现,我们确定了ACTH和AII的一个共同分子靶点。这两种肽对IAC的趋同抑制提示了一种机制,即起源于细胞膜的生化信号可被转导为依赖去极化的Ca2+内流和甾体激素分泌。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验