乙酰丁胺醇和心得安对不同离体血管平滑肌对5-羟色胺收缩反应的抑制作用。

S Shibata, S Ueda, N Satake
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摘要

对兔主动脉、基底动脉、肠系膜、肾动脉、股动脉、猫冠状动脉等大部分血管平滑肌对5-羟色胺(5-HT)的收缩反应进行预处理或高浓度的普萘洛尔预处理均有抑制作用。这两种药物的抑制作用通常大于对过量Ca2+和钾的反应。在兔肾动脉中,乙酰布洛尔对5-HT的反应没有影响,但对过量Ca2+和钾的反应有抑制作用。心得安对5-羟色胺反应有明显的抑制作用。在所有使用的制剂中,去甲肾上腺素(NE)和组胺诱导的收缩比5-HT、Ca2+和钾诱导的收缩表现出更大的抗乙酰丁醇和普萘洛尔的作用。硝苯地平在大多数制剂中对5-HT反应无抑制作用。硝苯地平仅抑制基底动脉对5-HT的反应。心得安对5-羟色胺反应的抑制作用大于乙酰丁醇。乙酰布洛尔和心得安对5-羟色胺反应的抑制作用可能与药物阻断β -肾上腺素受体作用以外的机制有关。讨论了两种β -肾上腺素受体拮抗剂对5-羟色胺抑制作用的可能机制。
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The inhibitory actions of acebutolol and propranolol on the contractile response to 5-hydroxytryptamine in various isolated vascular smooth muscles.

Pretreatment with acebutolol or propranolol at high concentrations had an inhibitory effect on the contractile response to 5-hydroxytryptamine (5-HT) in most vascular smooth muscles such as rabbit aorta and basilar, mesenteric, renal, femoral arteries and cat coronary artery. The inhibitory actions of both agents were generally greater than on the responses to excess Ca2+ and potassium. In rabbit renal arteries, acebutolol had no effect on the response to 5-HT but inhibited the responses to excess Ca2+ and potassium. Propranolol had a marked inhibitory effect on the response to 5-HT. In all preparations used, the contractions induced by norepinephrine (NE) and histamine showed a much greater resistance to the effect of acebutolol and propranolol than the contractions induced by 5-HT, Ca2+ and potassium. Nifedipine had no inhibitory effect on the response to 5-HT in most of the preparations. Nifedipine inhibited the response to 5-HT only in the basilar arteries. The inhibitory actions of propranolol on the response to 5-HT was greater than that of acebutolol. The inhibitory action of acebutolol and propranolol on the response to 5-HT may be related to mechanisms other than the beta-adrenoceptor blocking action of the drugs. The possible mechanisms of inhibitory action of both beta-adrenoceptor antagonists on 5-HT are discussed.

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