Effects of the beta-receptor antagonists propranolol, oxprenolol and labetalol on human vascular smooth-muscle contraction.

R F Moulds, R A Jauernig, J D Hobson, J Shaw
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引用次数: 8

Abstract

1. Spiral strips of human digital arteries have been studied in vitro to investigate whether DL-propranolol, D-propranolol, oxprenolol and labetalol have peripheral vascular effects in man. 2. Labetalol was a potent inhibitor of contractile responses to noradrenaline, but had less effect on responses to 5-hydroxytryptamine and barium chloride. 3. DL-and D-propranolol were equally effective inhibitors of responses to barium chloride. They were only weak antagonists of noradrenaline responses, but stronger, non-competitive antagonists of 5-hydroxytryptamine responses. 4. Oxprenolol was only a weak inhibitor of the responses to both noradrenaline and 5-hydroxytryptamine and had little effect on responses to barium chloride. 5. It is concluded that labetalol has specific alpha-adrenoreceptor-blocking properties, which are probably relevant to its therapeutic action in man. Propranolol has non-specific inhibitory effect on vascular smooth muscle, which might contribute to its hypotensive activity at high concentrations, but oxprenolol has only slight peripheral effects that are probably therapeutically insignificant.

受体拮抗剂心得安、奥普萘洛尔和拉贝他洛尔对人血管平滑肌收缩的影响。
1. 本文在体外研究人指动脉螺旋条,探讨dl -心得安、d -心得安、奥普萘洛尔和拉比他洛尔对人外周血管的影响。2. 拉贝他洛尔对去甲肾上腺素的收缩反应是一种有效的抑制剂,但对5-羟色胺和氯化钡的反应影响较小。3.dl -和d -心得安对氯化钡反应同样有效。它们只是去甲肾上腺素反应的弱拮抗剂,但对5-羟色胺反应具有较强的非竞争性拮抗剂。4. 奥普萘洛尔对去甲肾上腺素和5-羟色胺的抑制作用较弱,对氯化钡的抑制作用较小。5. 结论是,拉贝他洛尔具有特异性的α -肾上腺素受体阻断特性,这可能与其对人类的治疗作用有关。心得安对血管平滑肌有非特异性抑制作用,这可能有助于其在高浓度时的降压活性,但奥普萘洛尔只有轻微的外周作用,可能在治疗上无关紧要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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