Santiago J A, Osei S Y, Kadowitz P J
Department of Pharmacology, Tulane University School of Medicine, New Orleans, LA 70112.
Eur J Pharmacol. 1993 May 19;236(2):315-8. doi: 10.1016/0014-2999(93)90604-g.
The effect of Hoe 140, a bradykinin B2 receptor antagonist, on vasodilator responses to bradykinin was investigated in the mesenteric vascular bed of the cat under constant flow conditions. Injections of bradykinin into the mesenteric vascular bed induced dose-related decreases in perfusion pressure which were reduced significantly following administration of Hoe 140 (D-Arg-[Hyp3,Thi5,D-Tic7,Oic8]bradykinin) (100 micrograms/kg i.v.). The inhibitory effects of Hoe 140 were longer than 3 h in duration and vasodilator response to acetylcholine and S-nitroso-N-acetylpenicillamine and vasoconstrictor responses to norepinephrine, angiotensin II, and the thromboxane mimic, U46619 (9,11-dideoxy-11 alpha,9 alpha-epoxymethano-prostaglandin F2 alpha) were unchanged by the B2 receptor antagonist. Hoe 140 had little effect on baseline systemic arterial and mesenteric arterial perfusion pressures. These results suggest that Hoe 140 is a potent, highly selective, long-acting bradykinin B2 receptor antagonist with little agonistic activity in the mesenteric vascular bed of the cat.
在恒流条件下,研究了缓激肽B2受体拮抗剂Hoe 140(D-精氨酸-[Hyp3,Thi5,D-Tic7,Oic8]缓激肽)对猫肠系膜血管床中缓激肽血管舒张反应的影响。向肠系膜血管床注射缓激肽会引起灌注压呈剂量相关的下降,在静脉注射Hoe 140(100微克/千克)后,这种下降显著减轻。Hoe 140的抑制作用持续时间超过3小时,对乙酰胆碱和S-亚硝基-N-乙酰青霉胺的血管舒张反应以及对去甲肾上腺素、血管紧张素II和血栓素类似物U46619(9,11-二脱氧-11α,9α-环氧甲撑-前列腺素F2α)的血管收缩反应不受B2受体拮抗剂影响。Hoe 140对基础全身动脉和肠系膜动脉灌注压几乎没有影响。这些结果表明,Hoe 140是一种强效、高选择性、长效的缓激肽B2受体拮抗剂,在猫的肠系膜血管床中几乎没有激动活性。