Suppr超能文献

环磷酸腺苷(cAMP)激活兔膀胱上皮钠通道活性

Activation of epithelial Na(+) channel activity in the rabbit urinary bladder by cAMP.

作者信息

Burton T J, Elneil S, Nelson C P, Ferguson D R

机构信息

Department of Pharmacology, University of Cambridge, Tennis Court Road, CB2 1QJ, Cambridge, UK.

出版信息

Eur J Pharmacol. 2000 Sep 22;404(3):273-80. doi: 10.1016/s0014-2999(00)00597-5.

Abstract

The rabbit urinary bladder actively absorbs Na(+) from the urine. The rate-limiting step in this process is the diffusion of Na(+) across the apical membrane of bladder epithelial cells, mediated by amiloride-sensitive epithelial Na(+) channels. We have investigated the effects of cAMP on epithelial Na(+) channel activity in the rabbit bladder by measuring the amiloride-sensitive short-circuit current across bladders mounted in Ussing chambers. Three agents that raise intracellular cAMP levels (forskolin, dibutyryl-cAMP and 3-isobutyl-1-methylxanthine (IBMX)) increased the amiloride-sensitive short-circuit current relative to control preparations. The forskolin-induced increase in amiloride-sensitive short-circuit current was significantly inhibited by the vesicle fusion inhibitor brefeldin A and the protein synthesis inhibitor cycloheximide. These findings, together with the magnitude and protracted time course of the cAMP effects, suggests that cAMP stimulates the insertion of new Na(+) channels into the apical membrane of the rabbit bladder epithelium.

摘要

兔膀胱可主动从尿液中吸收Na⁺。这一过程的限速步骤是Na⁺经氨氯地平敏感的上皮Na⁺通道介导,跨膀胱上皮细胞顶端膜的扩散。我们通过测量置于尤斯灌流小室中的膀胱跨膜氨氯地平敏感短路电流,研究了环磷酸腺苷(cAMP)对兔膀胱上皮Na⁺通道活性的影响。三种可提高细胞内cAMP水平的试剂(福斯可林、二丁酰-cAMP和3-异丁基-1-甲基黄嘌呤(IBMX))相对于对照制剂,均增加了氨氯地平敏感短路电流。福斯可林诱导的氨氯地平敏感短路电流增加,被囊泡融合抑制剂布雷菲德菌素A和蛋白质合成抑制剂环己酰亚胺显著抑制。这些发现,连同cAMP效应的幅度和持久的时间进程,表明cAMP刺激新的Na⁺通道插入兔膀胱上皮的顶端膜。

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