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YM435在犬肾血管系统中的多巴胺DA1受体激动剂活性。

Dopamine DA1 receptor agonist activity of YM435 in the canine renal vasculature.

作者信息

Yatsu T, Uchida W, Inagaki O, Tanaka A, Takenaka T

机构信息

Cardiovascular and Atherosclerosis Research Laboratories, Ibaraki, Japan.

出版信息

Gen Pharmacol. 1997 Aug;29(2):229-32. doi: 10.1016/s0306-3623(96)00402-8.

Abstract
  1. The renal vasodilatory effect of YM435 was used as an index of its dopamine DA1 receptor agonist activity and compared with that of dopamine in pentobarbital-anesthetized dogs. 2. Intrarenal arterial administration of YM435 (0.1 to 10 micrograms) and dopamine (1 to 100 micrograms) produced a dose-dependent increase in renal blood flow. The doses of YM435 and dopamine required to cause a 30-ml/min increase in renal blood flow were 2.0 and 26.8 micrograms intra-arterially (IA), respectively. YM435 was therefore 13 times more potent than dopamine in this effect. 3. The selective dopamine DA1 receptor antagonist, SCH 23390, but not the selective dopamine DA2 receptor antagonist, nemonapride, caused dose-dependent, parallel shifts to the right in the dose-responsive curve of YM435. 4. The present results demonstrate that YM435 is a potent and selective dopamine DA1 receptor agonist.
摘要
  1. 将YM435的肾血管舒张作用作为其多巴胺DA1受体激动剂活性的指标,并与戊巴比妥麻醉犬体内多巴胺的作用进行比较。2. 肾内动脉注射YM435(0.1至10微克)和多巴胺(1至100微克)可使肾血流量呈剂量依赖性增加。肾血流量增加30毫升/分钟时,动脉内注射YM435和多巴胺所需剂量分别为2.0微克和26.8微克。因此,在此作用中YM435的效力是多巴胺的13倍。3. 选择性多巴胺DA1受体拮抗剂SCH 23390可使YM435的剂量反应曲线呈剂量依赖性、平行右移,而选择性多巴胺DA2受体拮抗剂奈莫必利则无此作用。4. 目前的结果表明,YM435是一种强效且选择性的多巴胺DA1受体激动剂。

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