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β-肾上腺素能受体拮抗剂DL 071 IT在人体的药效学研究。

Pharmacodynamic studies in man of the beta-adrenoceptor antagonist DL 071 IT.

作者信息

Radice M, Amanzio R, Criscuolo D

出版信息

Eur J Clin Pharmacol. 1979 Sep;16(2):87-90. doi: 10.1007/BF00563112.

Abstract

DL 071 IT, a new potent non-selective beta-adrenergic blocking drug with intrinsic sympathomimetic activity and weak membrane stabilizing activity, was evaluated alone and in comparison with oxprenolol, in six volunteers, at rest and during an exercise test. Heart rate and systolic pressure were monitored for up to 7 h after oral administration of the drugs. Exercise heart rate and systolic pressure were significantly reduced by both drugs, but only DL 071 IT caused a significant reduction in resting heart rate. As compared to oxprenolol, DL 071 IT has a longer duration of action and is from 5.0 to 13.5 times more potent.

摘要

DL 071 IT是一种新型强效非选择性β-肾上腺素能阻断药物,具有内在拟交感活性和较弱的膜稳定活性。在六名志愿者休息时及运动试验期间,对其单独使用并与氧烯洛尔进行比较进行了评估。口服药物后长达7小时监测心率和收缩压。两种药物均能显著降低运动时的心率和收缩压,但只有DL 071 IT能显著降低静息心率。与氧烯洛尔相比,DL 071 IT作用持续时间更长,效力强5.0至13.5倍。

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