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普萘洛尔或美托洛尔给药后对β-肾上腺素能刺激的代谢反应差异。

Differences in metabolic responses to beta-adrenergic stimulation after propranolol or metoprolol administration.

作者信息

William-Olsson T, Fellenius E, Björntorp P, Smith U

出版信息

Acta Med Scand. 1979;205(3):201-6. doi: 10.1111/j.0954-6820.1979.tb06031.x.

Abstract

Isoprenaline, or the beta 2-agonist terbutaline, was infused in healthy male volunteers and the plasma levels of insulin, glucose and free fatty acids (FFA) were determined. Saline, propranolol, or the selective beta 1-receptor antagonist, metoprolol, was administered i.v. prior to the infusion of the beta-stimulants. The two beta-receptor blockers inhibited isoprenaline-induced increase in chronotropy to about the same extent, while the effects on systolic and diastolic blood pressure were in accordance with a selective beta1-blocking effect of metoprolol and a non-selective beta-blocking action of propranolol. Quantitative differences were found between metoprolol and propranolol on the metabolic parameters. The effects can best be described in terms of beta 1- or beta 2-receptors, where effects on plasma FFA and glycerol levels seem to be mainly beta1-mediated. An apparent beta 2-mediated effect was found for insulin release and hepatic glucose output.

摘要

将异丙肾上腺素或β2激动剂特布他林注入健康男性志愿者体内,并测定其血浆胰岛素、葡萄糖和游离脂肪酸(FFA)水平。在注入β兴奋剂之前,静脉注射生理盐水、普萘洛尔或选择性β1受体拮抗剂美托洛尔。两种β受体阻滞剂对异丙肾上腺素引起的心率加快的抑制程度大致相同,而对收缩压和舒张压的影响则符合美托洛尔的选择性β1阻断作用和普萘洛尔的非选择性β阻断作用。美托洛尔和普萘洛尔在代谢参数上存在定量差异。这些作用最好用β1或β2受体来描述,其中对血浆FFA和甘油水平的影响似乎主要由β1介导。胰岛素释放和肝脏葡萄糖输出存在明显的β2介导效应。

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