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培哚普利在正常志愿者中的应用经验。

Experience with perindopril in normal volunteers.

作者信息

Waeber B, Nussberger J, Perret L, Santoni J P, Brunner H R

机构信息

Division of Hypertension, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.

出版信息

Arch Mal Coeur Vaiss. 1989 May;82 Spec No 1:35-41.

PMID:2549899
Abstract

The new orally active angiotensin converting enzyme (ACE) inhibitor perindopril was evaluated in normotensive men. Doses of 2 to 16 mg were given once a day for up to one week. Single oral doses of perindopril were found to blunt the pressor response to exogenous angiotensin I in a dose-dependent manner. The drug-induced ACE inhibition, as estimated by the measurement of plasma ACE activity, was maximal 4 to 8 hours post drug intake. ACE activity was still importantly reduced 24 hours after dosing. Plasma levels of angiotensin II and aldosterone decreased significantly whereas plasma renin activity and blood angiotensin I levels rose during peak ACE inhibition induced by the 4 and 8 mg doses. However, circulating levels of angiotensin II returned to baseline 24 hours after dosing, both on the first day of treatment and after one week of administration. ACE inhibition with perindopril did not affect blood pressure and heart rate in any consistent manner. There was no evidence for drug accumulation during repeated administration. The novel ACE inhibitor was well tolerated and produced no change in routine laboratory tests. The long-acting ACE inhibitor perindopril appears therefore to be effective when given orally in a dose range of 4 to 16 mg.

摘要

在血压正常的男性中对新型口服活性血管紧张素转换酶(ACE)抑制剂培哚普利进行了评估。每天给予2至16毫克剂量,持续长达一周。发现单次口服培哚普利能以剂量依赖的方式减弱对外源性血管紧张素I的升压反应。通过测量血浆ACE活性估计,药物诱导的ACE抑制在服药后4至8小时达到最大。给药24小时后,ACE活性仍显著降低。在4毫克和8毫克剂量诱导的ACE抑制峰值期间,血浆血管紧张素II和醛固酮水平显著下降,而血浆肾素活性和血血管紧张素I水平升高。然而,在治疗的第一天和给药一周后,给药24小时后循环血管紧张素II水平均恢复至基线。培哚普利抑制ACE并未以任何一致的方式影响血压和心率。重复给药期间没有药物蓄积的证据。这种新型ACE抑制剂耐受性良好,常规实验室检查无变化。因此,长效ACE抑制剂培哚普利口服4至16毫克剂量时似乎有效。

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