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钙拮抗剂TMB - 8对兔回肠主动钠和氯转运的影响。

Effects of calcium antagonist TMB-8 on active Na and Cl transport in rabbit ileum.

作者信息

Donowitz M, Cusolito S, Sharp G W

出版信息

Am J Physiol. 1986 May;250(5 Pt 1):G691-7. doi: 10.1152/ajpgi.1986.250.5.G691.

Abstract

The effects of 3,4,5-trimethoxybenzoate 8-(N,N-diethylamino)octyl ester (TMB-8), an agent that traps calcium within intracellular stores, were studied on active electrolyte transport in rabbit ileum under basal conditions and after altering transport by increasing the intracellular cAMP content or by exposure to two agonists that act by altering intracellular Ca2+ (carbachol and serotonin). TMB-8 decreased the ileal short-circuit current and increased active Na and Cl absorption by increasing the mucosal-to-serosal Na and Cl fluxes. These effects were reversed by increasing the bathing solution Ca2+ to 4 mM, a concentration that itself did not alter basal ileal transport. The maximum glucose- and amino acid (alanine)-induced increase in Na absorption in the ileum was not affected by TMB-8. The effects on basal transport of TMB-8 were not associated with a change in 45Ca2+ entry across the ileal serosal surface. TMB-8 did not alter cAMP-induced secretion, as judged by its lack of effect on the increase in short-circuit current caused by 8-bromo-cAMP (10(-4) M). TMB-8 totally prevented the transport effects of carbachol but did not inhibit the effects of serotonin. These data suggest a role for intracellular Ca2+ in regulation of basal ileal Na and Cl transport but not in cAMP-induced secretion. There appear to be several pools of intracellular Ca2+ involved in neurohumoral effects on active electrolyte transport.

摘要

研究了3,4,5-三甲氧基苯甲酸8-(N,N-二乙氨基)辛酯(TMB-8),一种将钙捕获在细胞内储存库中的试剂,对基础条件下家兔回肠主动电解质转运的影响,以及在通过增加细胞内cAMP含量或暴露于两种通过改变细胞内Ca2+起作用的激动剂(卡巴胆碱和5-羟色胺)来改变转运后对其的影响。TMB-8通过增加黏膜到浆膜的Na和Cl通量,降低了回肠短路电流,并增加了主动Na和Cl吸收。将浴液Ca2+增加到4 mM可逆转这些效应,该浓度本身不会改变基础回肠转运。TMB-8不影响回肠中葡萄糖和氨基酸(丙氨酸)诱导的Na吸收的最大增加。TMB-8对基础转运的影响与跨回肠浆膜表面的45Ca2+进入变化无关。根据TMB-8对8-溴-cAMP(10(-4) M)引起的短路电流增加缺乏影响判断,它不改变cAMP诱导的分泌。TMB-8完全阻止了卡巴胆碱的转运效应,但不抑制5-羟色胺的效应。这些数据表明细胞内Ca2+在基础回肠Na和Cl转运的调节中起作用,但在cAMP诱导的分泌中不起作用。在神经体液对主动电解质转运的影响中,似乎有几个细胞内Ca2+池参与其中。

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