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大鼠皮质集合管中钠通道的反馈调节。I. 钠泵抑制的作用

Feedback regulation of Na channels in rat CCT. I. Effects of inhibition of Na pump.

作者信息

Silver R B, Frindt G, Windhager E E, Palmer L G

机构信息

Department of Physiology and Biophysics, Cornell University Medical College, New York, New York 10021.

出版信息

Am J Physiol. 1993 Mar;264(3 Pt 2):F557-64. doi: 10.1152/ajprenal.1993.264.3.F557.

Abstract

Na channels in the apical membrane of the rat renal cortical collecting tubule were studied using the patch-clamp technique. Channel activity was monitored in cell-attached patches on tubules that were split open to expose the luminal surface. Channel number (N), open probability (Po), and currents (i) were measured at 37 degrees C during continuous superfusion of the tubule. Addition of ouabain (1 mM) to the superfusate to increase cell Na resulted in a decrease in the mean number of open channels (NPo) to less than 20% of control values within 2 min. This effect was not reversible within 5 min after removal of ouabain. There was, in addition, a parallel decrease in i. The mechanism of inhibiton appeared to involve increased intracellular Ca (Cai). Cai was measured using the fluorescence of the Ca indicator fura-2 in principal cells of split tubules under conditions identical to those used for electrical measurements. Cai increased from a basal level (153 +/- 36 nM) to a peak level (588 +/- 53 nM) approximately 3 min after the addition of ouabain. When a Ca-free superfusate was used, ouabain did not increase Cai or decrease NPo, although the decrease in i was similar to that observed in Ca-containing solutions. Similar increases in Cai were elicited by the Ca ionophore ionomycin (5 microM) in the presence of 0.1 mM extracellular Ca. This maneuver also resulted in a decrease in NPo which was similar to that observed in the presence of ouabain. Ouabain had no observable effect on cell pH.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

运用膜片钳技术研究了大鼠肾皮质集合管顶端膜中的钠通道。在将小管劈开以暴露管腔表面的情况下,监测细胞贴附式膜片中的通道活性。在37℃下持续灌流小管时,测量通道数量(N)、开放概率(Po)和电流(i)。向灌流液中添加哇巴因(1 mM)以增加细胞内钠,导致开放通道的平均数量(NPo)在2分钟内降至对照值的20%以下。去除哇巴因后5分钟内,这种效应不可逆。此外,i也平行下降。抑制机制似乎涉及细胞内钙(Cai)增加。在与电测量相同的条件下,使用钙指示剂fura-2的荧光在劈开小管的主细胞中测量Cai。添加哇巴因后约3分钟,Cai从基础水平(153±36 nM)升至峰值水平(588±53 nM)。当使用无钙灌流液时,哇巴因不会增加Cai或降低NPo,尽管i的下降与在含钙溶液中观察到的相似。在存在0.1 mM细胞外钙的情况下,钙离子载体离子霉素(5 microM)也引起了类似的Cai增加。这种操作也导致NPo下降,与在哇巴因存在下观察到的相似。哇巴因对细胞pH没有明显影响。(摘要截短于250字)

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