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阿片类物质抑制大鼠肾脏对醛固酮反应中的多巴胺能增强作用。

Opiates inhibit the dopaminergic enhancement of the renal response to aldosterone in the rat.

作者信息

Adam W R, Danks J A, Goland G

出版信息

Clin Exp Pharmacol Physiol. 1981 Sep-Oct;8(5):549-52. doi: 10.1111/j.1440-1681.1981.tb00765.x.

Abstract
  1. Both naloxone, an opiate antagonist, and levorphanol, an opiate agonist, inhibit the enhanced renal response to aldosterone produced by both l-dopa pretreatment and a high K+ diet. 2. This supports the evidence for a common mechanism of action for the enhancement of the renal response to aldosterone produced by l-dopa and a high K+ diet. Whether this mechanism is dopaminergic or opiate is uncertain. 3. The inhibition of the enhanced response, produced by l-dopa, by opiates is consistent with previous findings of displacement of 3H-dopamine from renal homogenates by opiates and supports the hypothesis that the binding sites relate to the renal response to aldosterone.
摘要
  1. 阿片类拮抗剂纳洛酮和阿片类激动剂左啡诺,均能抑制左旋多巴预处理和高钾饮食所产生的肾脏对醛固酮反应增强的现象。2. 这支持了左旋多巴和高钾饮食增强肾脏对醛固酮反应存在共同作用机制的证据。该机制是多巴胺能的还是阿片类的尚不确定。3. 阿片类药物对左旋多巴所产生的增强反应的抑制作用,与之前阿片类药物使肾匀浆中的3H-多巴胺发生位移的研究结果一致,并支持了与肾脏对醛固酮反应相关的结合位点这一假说。

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