Frindt G, Silver R B, Windhager E E, Palmer L G
Department of Physiology and Biophysics, Cornell University Medical College, New York, New York 10021.
Am J Physiol. 1995 Mar;268(3 Pt 2):F480-9. doi: 10.1152/ajprenal.1995.268.3.F480.
The effects of exogenous adenosine 3',5'-cyclic monophosphate (cAMP) on apical Na channels in the rat cortical collecting tubule were studied using the patch-clamp technique and fura 2 fluorescence measurements of intracellular Ca2+ (Ca2+i). When the permeant analogue, 8-(4-chlorophenylthio)-cAMP (CPT-cAMP, 200 microM), was added to the superfusate during recording from cell-attached patches, both the mean number of open channels (NPo) and the single-channel current (i) decreased within 3 min. When the superfusate also contained amiloride (10 microM), there was no effect of CPT-cAMP on either NPo or i. When CPT-cAMP was added to the bath before formation of the patch, the density of conducting channels was increased from 10 +/- 2 to 37 +/- 6 per patch, as estimated by analysis of channel-induced noise. This suggests that cAMP increases open-channel density in the regions of the apical membrane outside the patch but not within the patch. Channels already active in the patch before stimulation with the nucleotide are subject to feedback inhibition secondary to increased Na entry into the cell. CPT-cAMP increased Ca2+i from 104 to 198 nM. This increase in Ca2+i was abolished by benzamil (0.5 microM) or by low extracellular Ca2+. The cAMP-dependent reduction in NPo was still observed in Ca(2+)-free medium, indicating that a rise in Ca2+i was not essential for the feedback response. The decrease in NPo was attenuated, however, when cAMP was added in the absence of Ca2+ and in the presence of ouabain (1 mM) in the superfusate.(ABSTRACT TRUNCATED AT 250 WORDS)
利用膜片钳技术和fura 2荧光法测量细胞内钙离子(Ca2+i),研究了外源性3',5'-环磷酸腺苷(cAMP)对大鼠皮质集合管顶端钠通道的影响。在细胞贴附式膜片记录过程中,当向灌流液中加入可渗透类似物8-(4-氯苯硫基)-cAMP(CPT-cAMP,200 microM)时,开放通道的平均数量(NPo)和单通道电流(i)在3分钟内均下降。当灌流液中还含有氨氯吡脒(10 microM)时,CPT-cAMP对NPo或i均无影响。在形成膜片前将CPT-cAMP加入浴液中,通过对通道诱发噪声的分析估计,每个膜片传导通道的密度从10±2增加到37±6。这表明cAMP增加了膜片外顶端膜区域的开放通道密度,但膜片内没有增加。在用核苷酸刺激之前已经在膜片中活跃的通道,由于进入细胞的钠增加而受到反馈抑制。CPT-cAMP使Ca2+i从104 nM增加到198 nM。苯甲酰胺(0.5 microM)或低细胞外钙可消除Ca2+i的这种增加。在无钙培养基中仍观察到cAMP依赖性的NPo降低,表明Ca2+i的升高对于反馈反应并非必需。然而,当在灌流液中无钙且存在哇巴因(1 mM)的情况下加入cAMP时,NPo的降低减弱。(摘要截短于250字)