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利尿剂和血管加压素对蛙膀胱渗透通透性的影响。

The effect of diuretics and vasopressin on the osmotic permeability of the frog urinary bladder.

作者信息

Natochin Y V, Shakhmatova E I

出版信息

Physiol Bohemoslov. 1976;25(6):529-34.

PMID:139627
Abstract
  1. Large concentrations (in mM) of ethacrynic acid (0.1), furosemide (1.0), theophylline (5.0) and osmotic diuretics (100.0) sharply increased the flux of water along an osmotic gradient through the frog urinary bladder wall. Spironolactone (0.1), and hydrochlorothiazide (5.0) showed only a weak action on osmotic permeability. MercusalR, clopamide and triamterene did not affect water transport. 2. The presence of 0.2--1.0 mU/ml vasopressin (ADH) after pretreatment with a diuretic did not result in summation of the effects of both drugs used. 0.01--0.1 mM ethacrynic acid and 0.01 mM MercusalR significantly decreased the reaction to ADH. 1.0 mM furosemide, 0.1 mM spironolactone, 0.01 mM clopamide and 0.8 mM acetazolamide did not change the reaction to ADH. A reduction in the cellular response to ADH and a decrease in the osmotic permeability of the tubular wall may be responsible in part for the diuretic action of ethacrynic acid and MercusalR.
摘要
  1. 高浓度(以毫摩尔计)的依他尼酸(0.1)、呋塞米(1.0)、茶碱(5.0)和渗透性利尿剂(100.0)能显著增加水沿渗透梯度通过蛙膀胱壁的通量。螺内酯(0.1)和氢氯噻嗪(5.0)对渗透通透性仅表现出微弱作用。汞撒利、氯帕胺和氨苯蝶啶对水转运无影响。2. 用利尿剂预处理后加入0.2 - 1.0 毫单位/毫升的血管加压素(抗利尿激素,ADH),并未使两种药物的作用相加。0.01 - 0.1毫摩尔的依他尼酸和0.01毫摩尔的汞撒利显著降低了对ADH的反应。1.0毫摩尔的呋塞米、0.1毫摩尔的螺内酯、0.01毫摩尔的氯帕胺和0.8毫摩尔的乙酰唑胺未改变对ADH的反应。细胞对ADH反应的降低以及肾小管壁渗透通透性的下降可能部分解释了依他尼酸和汞撒利的利尿作用。

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