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

被引:5
作者
Burton, TJ [1 ]
Elneil, S [1 ]
Nelson, CP [1 ]
Ferguson, DR [1 ]
机构
[1] Univ Cambridge, Dept Pharmacol, Cambridge CB2 1QJ, England
关键词
epithelial Na+ channel; cAMP; urinary bladder;
D O I
10.1016/S0014-2999(00)00597-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:273 / 280
页数:8
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