静脉和口服给药后品多洛尔的临床药理学研究。

Advances in clinical pharmacology Pub Date : 1976-01-01
W H Aellig
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引用次数: 0

摘要

通过健康志愿者的临床药理学实验,比较品多洛尔经静脉和口服后对肾上腺素受体的阻断作用。等剂量品多洛尔在静脉注射后75分钟和口服给药后2小时对因异丙肾上腺素输注引起的心动过速以及在循环计力器上因运动引起的心动过速具有同等作用。药效学效果的比较结果证实了在药代动力学研究中报道的良好的肠内吸收。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Clinicopharmacological studies with pindolol following intravenous and oral administration].

The beta-adrenoceptor blocking potency of pindolol after intravenous and after oral administration was compared in clinical pharmacological experiments in healthy volunteers. Equal doses of pindolol were aequiactive 75 min after intravenous and 2 h after oral administration on tachycardia due to isoprenaline infusions as well as on tachycardia due to exercise on the cycle ergometer. The results of this comparison of pharmacodynamic effects confirm the good enteral absorption reported in pharmacokinetic studies.

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