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水和钠的转运:钙通道阻滞剂和钙调蛋白拮抗剂对两栖类上皮细胞顶端膜和基底外侧膜的影响。

Water and sodium transport: effects of calcium channel blocker and calmodulin antagonists on the apical and basolateral membranes of amphibian epithelia.

作者信息

Shakhmatova E I, Bakos P

出版信息

Gen Physiol Biophys. 1987 Feb;6(1):35-44.

PMID:2885243
Abstract

Ca2+ channel blocker (sensit) and calmodulin antagonists (thioridazine, perphenazine, oxyprothepine) applied to the mucosal side of frog urinary bladder, weakened the response of epithelial cells to vasopressin. Thioridazine (2.7 X 10(-5) mol X l-1) and sensit (1.7 X 10(-4) mol X l-1) applied to the serosal side rapidly increased the permeability of the epithelia for sodium and potassium ions along the concentration gradient (from serosa to mucosa). The same concentrations of these blockers when applied to the mucosal side of frog urinary bladder selectively decreased vasopressin stimulated water permeability and did not influence ionic permeability. Both thioridazine and sensit decreased the short-circuit current across frog skin. The results show that the Ca2+ channel blocker and the calmodulin antagonists tested influenced water and ionic transport across the epithelial cell membranes, and had different effects upon the apical and the basolateral cell membranes.

摘要

将钙离子通道阻滞剂(sensit)和钙调蛋白拮抗剂(硫利达嗪、奋乃静、奥昔丙嗪)应用于蛙膀胱黏膜侧,会减弱上皮细胞对血管加压素的反应。将硫利达嗪(2.7×10⁻⁵摩尔×升⁻¹)和sensit(1.7×10⁻⁴摩尔×升⁻¹)应用于浆膜侧,会使上皮细胞对钠离子和钾离子的通透性沿着浓度梯度(从浆膜到黏膜)迅速增加。当将相同浓度的这些阻滞剂应用于蛙膀胱黏膜侧时,会选择性地降低血管加压素刺激的水通透性,而不影响离子通透性。硫利达嗪和sensit均会降低蛙皮肤的短路电流。结果表明,所测试的钙离子通道阻滞剂和钙调蛋白拮抗剂影响了上皮细胞膜的水和离子转运,并且对顶端和基底外侧细胞膜有不同的作用。

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