Kinter L B, Horner E, Mann W A, Weinstock J, Ruffolo R R
Department of Pharmacology, Smith Kline Beecham Pharmaceuticals, King of Prussia, Pennsylvania 19406-0939.
Chirality. 1990;2(4):219-25. doi: 10.1002/chir.530020405.
Fenoldopam (SK&F 82526) is a potent and selective dopamine DA-1 agonist with demonstrated renal vasodilator and antihypertensive activities in experimental animals and humans. Fenoldopam is a racemic mixture of two enantiomers, SK&F R-82526 and SK&F S-82526. The R-enantiomer is uniformly reported to be more potent than the racemate; in contrast, there is controversy regarding potency of the S-enantiomer. In these studies, the renal and systemic hemodynamic activities of fenoldopam and its enantiomers are characterized in anesthetized, phenoxybenzamine-treated dogs. The results show that the renal and systemic vasodilator activities of fenoldopam are properties of the R-enantiomer; the S-enantiomer is essentially inactive. The renal and systemic vasodilator properties of SK&F R-82526 are antagonized in a competitive fashion by the DA-1 antagonist, SK&F R-83566, but not the DA-2 antagonist, domperidone. Ganglionic blockade did not attenuate renal vasodilation associated with SK&F R-82526. Thus, the mechanism of SK&F R-82526-associated vasodilation, like that previously established for fenoldopam, is via stimulation of postganglionic DA-1 receptors.
非诺多泮(SK&F 82526)是一种强效且选择性的多巴胺DA-1激动剂,在实验动物和人类中已证实具有肾血管舒张和降压活性。非诺多泮是两种对映体SK&F R-82526和SK&F S-82526的外消旋混合物。一致报道R-对映体比外消旋体更具活性;相比之下,关于S-对映体的活性存在争议。在这些研究中,对经苯氧苄胺处理的麻醉犬的非诺多泮及其对映体的肾脏和全身血流动力学活性进行了表征。结果表明,非诺多泮的肾脏和全身血管舒张活性是R-对映体的特性;S-对映体基本无活性。SK&F R-82526的肾脏和全身血管舒张特性被DA-1拮抗剂SK&F R-83566以竞争性方式拮抗,但不被DA-2拮抗剂多潘立酮拮抗。神经节阻断并未减弱与SK&F R-82526相关的肾血管舒张。因此,与SK&F R-82526相关的血管舒张机制,与先前为非诺多泮确立的机制一样,是通过刺激节后DA-1受体。