(3H)-吡列脲与肾髓质特定受体的结合。

Journal de pharmacologie Pub Date : 1986-04-01
E M Giesen-Crouse, P Fandeleur, J L Imbs
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引用次数: 0

摘要

我们以前已经证明(3H)-吡列他胺与位于犬肾髓膜上的受体结合。在这里,我们表明结合是特定的一组环利尿剂。苯甲酸家族的磺酰胺利尿剂、其他取代的磺酰胺和苯氧乙酸衍生物从其受体取代(3H)-吡脲。不作用于管状管膜的环状利尿剂不会取代吡他尼,不同部位和作用方式的利尿剂也不会取代吡他尼(噻嗪类;Na+/H+反转运蛋白(阿米洛利)、Na+K+ atp酶(瓦巴因)或碳酸酐酶(乙酰唑胺)的抑制剂。我们证明吡列胺受体和几种神经递质的膜结合受体之间没有干扰。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Binding of (3H)-piretanide to a specific receptor of renal medulla.

We had previously demonstrated that (3H)-piretanide binds to a receptor located on medullary membranes of canine kidney. Here we show that binding is specific for a particular group of loop diuretics. Sulfonamide diuretics of the benzoic acid family, other substituted sulfonamides, and phenoxy-acetic acid derivates displace (3H)-piretanide from its receptor. Loop diuretics that do not act at the luminal tubular membrane do not displace piretanide, nor do diuretics with a different site and mode of action (thiazides; inhibitors of the Na+/H+ antiporter (amiloride), of Na+K+ ATPase (ouabain), or of carbonic anhydrase (acetazolamide). We demonstrate that no interference occurs between the piretanide receptor and membrane bound receptors of several neurotransmitters.

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