Ohlstein E H, Zabko-Potapovich B, Berkowitz B A
Eur J Pharmacol. 1985 Dec 3;118(3):321-9. doi: 10.1016/0014-2999(85)90143-8.
The alpha-adrenoceptor activity of fenoldopam was evaluated in three different in vitro tissue preparations. In rabbit isolated aortic rings fenoldopam displayed weak alpha 1-adrenoceptor antagonist activity (-log KB = 5.41) and displayed no alpha 1-adrenoceptor agonist activity. In contrast, fenoldopam demonstrated moderately potent antagonist properties at the alpha 2-adrenoceptor in two other tissue preparations. In in vitro model systems used for the characterization of alpha 2-adrenoceptors, fenoldopam competitively antagonized the effects of the alpha 2-adrenoceptor agonist B-HT 920. In the dog isolated saphenous vein and in the isolated field-stimulated guinea-pig ileum, fenoldopam antagonized the effects of B-HT 920 with -log KB values of 7.78 and 7.60, respectively. These data indicate that in addition to being an agonist at DA1 receptors, fenoldopam is also a relatively selective antagonist at alpha 2-adrenoceptors.
在三种不同的体外组织制备物中评估了非诺多泮的α-肾上腺素能受体活性。在兔离体主动脉环中,非诺多泮表现出较弱的α1-肾上腺素能受体拮抗剂活性(-log KB = 5.41),且未表现出α1-肾上腺素能受体激动剂活性。相比之下,在另外两种组织制备物中,非诺多泮在α2-肾上腺素能受体上表现出中等强度的拮抗剂特性。在用于表征α2-肾上腺素能受体的体外模型系统中,非诺多泮竞争性拮抗α2-肾上腺素能受体激动剂B-HT 920的作用。在犬离体隐静脉和离体场刺激的豚鼠回肠中,非诺多泮拮抗B-HT 920的作用,其-log KB值分别为7.78和7.60。这些数据表明,非诺多泮除了是DA1受体激动剂外,还是α2-肾上腺素能受体的相对选择性拮抗剂。