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.

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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。
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