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锶诱导的自发性出汗期间的跨上皮电位

Transepithelial potential during strontium-induced spontaneous sweating.

作者信息

Sato K, Sato F

出版信息

Am J Physiol. 1982 May;242(5):C360-5. doi: 10.1152/ajpcell.1982.242.5.C360.

DOI:10.1152/ajpcell.1982.242.5.C360
PMID:7044137
Abstract

Transepithelial electrical potential difference (PD) of the secretory portion of the rhesus monkey palm eccrine sweat gland was studied in both Ca2+-containing (control and Ca2+-free Sr2+ media. In the control medium, the luminal PD was a saturation function of the methacholine (MCH) concentration, reaching a plateau at about -6 mV (lumen negative) at 10(-5) M MCH. In the Sr2+ medium, the luminal PD increased spontaneously with a time course similar to that the spontaneous sweat secretion (SSS). Like SSS, the spontaneous luminal PD in the Sr2+ medium is a saturation function of the Sr2+ concentration in the bath, reaching a plateau at -9 mV at 8 mM Sr2+. Addition of MCH to the Sr2+ medium caused a rapid increase in the lumen-negative PD as seen in the control medium. The spontaneous lumen-negative PD was abolished by subsequent addition of Ca2+ to the bath, as was the SSS [K. Sato, Am. J. Physiol. 239 (Cell Physiol. 8): C90-C97, 1980]. The data further reinforce the notion that Sr2+-induced SSS represents true secretory processes which are triggered by Sr2+ leaking into the cell bypassing the receptor-agonist interaction.

摘要

在含Ca2+(对照)和无Ca2+的Sr2+培养基中,研究了恒河猴手掌小汗腺分泌部的跨上皮电位差(PD)。在对照培养基中,管腔PD是乙酰甲胆碱(MCH)浓度的饱和函数,在10(-5) M MCH时达到约-6 mV(管腔为负)的平台期。在Sr2+培养基中,管腔PD随时间自发增加,其时间进程与自发汗液分泌(SSS)相似。与SSS一样,Sr2+培养基中的自发管腔PD是浴液中Sr2+浓度的饱和函数,在8 mM Sr2+时达到-9 mV的平台期。向Sr2+培养基中添加MCH会导致管腔负PD迅速增加,这与对照培养基中所见情况相同。随后向浴液中添加Ca2+可消除自发的管腔负PD,SSS也会被消除[K. 佐藤,《美国生理学杂志》239(细胞生理学8):C90 - C97,1980]。这些数据进一步强化了这样一种观点,即Sr2+诱导的SSS代表了真正的分泌过程,该过程是由Sr2+绕过受体 - 激动剂相互作用泄漏到细胞中所触发的。

相似文献

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Transepithelial potential during strontium-induced spontaneous sweating.锶诱导的自发性出汗期间的跨上皮电位
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Effect of methacholine on ionic permeability of basal membrane of the eccrine secretory cell.乙酰甲胆碱对小汗腺分泌细胞基底膜离子通透性的影响。
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J Physiol. 1987 Dec;393:195-212. doi: 10.1113/jphysiol.1987.sp016819.