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龟结肠顶端钠通道的胆碱能调节:对CDPC诱导波动的分析

Cholinergic modulation of apical Na+ channels in turtle colon: analysis of CDPC-induced fluctuations.

作者信息

Wilkinson D J, Dawson D C

机构信息

Department of Physiology, University of Michigan Medical School, Ann Arbor 48109.

出版信息

Am J Physiol. 1990 Oct;259(4 Pt 1):C668-74. doi: 10.1152/ajpcell.1990.259.4.C668.

Abstract

Current fluctuation analysis was used to investigate the properties of apical Na+ channels during muscarinic inhibition of active Na+ absorption. A reversible Na+ channel blocker, 6-chloro-3,5-diaminopyrazine-2-carboxamide (CDPC), was used to induce fluctuations in the short-circuit current (I(sc)). Power density spectra of the CDPC-induced fluctuations exhibited a clearly discernible Lorentzian component, characterized by a corner frequency that was linearly related to CDPC concentration between 20 and 100 microM. The on (k'on) and off (k(off)) rate coefficients for the CDPC blocking reaction were k'on = 11.1 +/- 0.8 rad.s-1.microM-1 and k(off) = 744 +/- 53 rad/s, and the microscopic inhibition constant was 67 microM (n = 11). CDPC blocking kinetics were not significantly different after inhibition of Isc by 5 microM serosal carbachol. Single-channel Na+ current (iNa) and the density of open and blocked Na+ channels (N(ob)) were estimated from the fluctuations induced by 40 microM CDPC. Under control conditions, iNa was 0.43 +/- 0.05 pA and N(ob) was 251 +/- 42 X 10(6)/cm2 (n = 10). After exposure to serosal carbachol (2-10 microM) for 60 min, Na+ current and N(ob) were reduced by approximately 50%, but iNa was not changed significantly. These results indicate that muscarinic inhibition of electrogenic Na+ absorption was associated with a reduction in the number of open Na+ channels in the apical membrane. They also suggest that this downregulation of transport involved a coordinated decrease in both apical and basolateral membrane conductances.

摘要

运用电流波动分析来研究毒蕈碱抑制主动钠吸收过程中顶端钠通道的特性。使用一种可逆的钠通道阻滞剂6-氯-3,5-二氨基吡嗪-2-甲酰胺(CDPC)来诱导短路电流(I(sc))的波动。CDPC诱导波动的功率密度谱呈现出明显可辨的洛伦兹分量,其特征频率与20至100微摩尔浓度范围内的CDPC浓度呈线性相关。CDPC阻断反应的开启(k'on)和关闭(k(off))速率系数分别为k'on = 11.1 ± 0.8弧度·秒-1·微摩尔-1和k(off) = 744 ± 53弧度/秒,微观抑制常数为67微摩尔(n = 11)。在5微摩尔浆膜侧卡巴胆碱抑制Isc后,CDPC的阻断动力学没有显著差异。从40微摩尔CDPC诱导的波动中估计单通道钠电流(iNa)以及开放和阻断钠通道的密度(N(ob))。在对照条件下,iNa为0.43 ± 0.05皮安,N(ob)为251 ± 42×10(6)/平方厘米(n = 10)。暴露于浆膜侧卡巴胆碱(2 - 10微摩尔)60分钟后,钠电流和N(ob)降低了约50%,但iNa没有显著变化。这些结果表明,毒蕈碱对电生性钠吸收的抑制与顶端膜中开放钠通道数量的减少有关。它们还表明,这种转运下调涉及顶端和基底外侧膜电导的协同降低。

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