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氨氯吡咪对两栖动物上皮细胞中钠离子通道的阻断作用并不需要细胞外的钙离子。

Amiloride blockage of Na+ channels in amphibian epithelia does not require external Ca2+.

作者信息

Desmedt L, Simaels J, Van Driessche W

机构信息

Laboratory for Physiology, KULeuven, Belgium.

出版信息

Pflugers Arch. 1991 Dec;419(6):632-8. doi: 10.1007/BF00370307.

DOI:10.1007/BF00370307
PMID:1664939
Abstract

Noise analysis was used to study the influence of external Ca2+ on the blockage of Na+ transport by amiloride. Experiments were done using frog skin (Rana temporaria and Rana catesbeiana), toad urinary bladder (Bufo marinus) and epithelia of A6 cells. In nondepolarized skins and bladders, removal of Ca2+ from the mucosal bath diminished markedly the inhibitory effect of amiloride. Ca2+ depletion also gave rise to the appearance of an additional noise component related to cation movement through the poorly selective cation channel in the apical membrane [Aelvoet I, Erlij D, Van Driessche W (1988) J Physiol (Lond) 398:555-574; Van Driessche W, Desmedt L, Simaels J (1991) Pflügers Arch 418:193-203]. The amplitude of this Ca(2+)-blockable noise component was elevated by amiloride and markedly exceeded the amiloride-induced Lorentzian noise levels as recorded in the presence of Ca2+. On the other hand, in K(+)-depolarized skins and bladders as well as in nondepolarized epithelial of A6 cells, the Ca(2+)-blockable noise was absent or of much smaller amplitude. Depolarization of frog skin and toad urinary bladder apparently inactivated the poorly selective channels, whereas in A6 cells they were not observed. Under these conditions the typical amiloride-induced blocker noise could also be analysed in the absence of Ca2+ and demonstrated that the on and off rates for amiloride binding were not significantly altered by external Ca2+.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

噪声分析被用于研究细胞外钙离子对氨氯地平阻断钠离子转运的影响。实验使用了蛙皮(林蛙和牛蛙)、蟾蜍膀胱(海蟾蜍)以及A6细胞的上皮组织。在未去极化的皮肤和膀胱中,去除黏膜浴中的钙离子会显著减弱氨氯地平的抑制作用。钙离子耗竭还会导致出现一种额外的噪声成分,该成分与阳离子通过顶端膜中选择性较差的阳离子通道的移动有关[Aelvoet I, Erlij D, Van Driessche W (1988) J Physiol (Lond) 398:555 - 574; Van Driessche W, Desmedt L, Simaels J (1991) Pflügers Arch 418:193 - 203]。这种可被钙离子阻断的噪声成分的幅度会因氨氯地平而升高,且明显超过在有钙离子存在时记录到的氨氯地平诱导的洛伦兹噪声水平。另一方面,在钾离子去极化的皮肤和膀胱以及未去极化的A6细胞上皮组织中,可被钙离子阻断的噪声不存在或幅度小得多。蛙皮和蟾蜍膀胱的去极化显然使选择性较差的通道失活,而在A6细胞中未观察到这种情况。在这些条件下,典型的氨氯地平诱导的阻断剂噪声也可在无钙离子的情况下进行分析,结果表明氨氯地平结合的开启和关闭速率并未因细胞外钙离子而发生显著改变。(摘要截选至250词)

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本文引用的文献

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Mechanism of ion permeation through calcium channels.离子通过钙通道的渗透机制。
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Noise analysis of inward and outward Na+ currents across the apical border of ouabain-treated frog skin.哇巴因处理的蛙皮顶端边界处内向和外向钠离子电流的噪声分析
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Poorly selective cation channels in the apical membrane of A6 cells.A6细胞顶端膜中选择性差的阳离子通道。
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J Gen Physiol. 1983 Aug;82(2):201-20. doi: 10.1085/jgp.82.2.201.
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The role of calcium ions in the interaction of amiloride with membrane receptors.钙离子在氨氯吡咪与膜受体相互作用中的作用。
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6
Dexamethasone accelerates differentiation of A6 epithelia and increases response to vasopressin.地塞米松可加速 A6 上皮细胞的分化,并增强对血管加压素的反应。
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Correction of proton and Ca association constants of EGTA for temperature and ionic strength.校正乙二醇双(2-氨基乙基醚)四乙酸(EGTA)的质子和钙结合常数以考虑温度和离子强度的影响 。
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Activation and blockage of a calcium-sensitive cation-selective pathway in the apical membrane of toad urinary bladder.蟾蜍膀胱顶端膜中钙敏感阳离子选择性通道的激活与阻断
J Physiol. 1988 Apr;398:555-74. doi: 10.1113/jphysiol.1988.sp017057.
9
Oxytocin and cAMP stimulate monovalent cation movements through a Ca2+-sensitive, amiloride-insensitive channel in the apical membrane of toad urinary bladder.催产素和环磷酸腺苷通过蟾蜍膀胱顶端膜中对钙离子敏感、对氨氯吡脒不敏感的通道刺激单价阳离子运动。
Proc Natl Acad Sci U S A. 1987 Jan;84(1):313-7. doi: 10.1073/pnas.84.1.313.
10
Effect of sodium on amiloride- and triamterene-induced current fluctuations in isolated frog skin.钠对离体蛙皮中氨氯吡咪和氨苯蝶啶诱导的电流波动的影响。
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