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阿拉普利代谢产物和赖诺普利的自由基清除特性。

Free radical scavenging properties of alacepril metabolites and lisinopril.

作者信息

Noda Y, Mori A, Packer L

机构信息

Department of Molecular and Cell Biology, University of California, Berkeley 94720-3200, USA.

出版信息

Res Commun Mol Pathol Pharmacol. 1997 May;96(2):125-36.

PMID:9226747
Abstract

Alacepril is an inhibitor of the angiotensin converting enzyme (ACE), and is commonly used as an antihypertensive. In this study, the effects of alacepril, its metabolites, desacetylalacepril and captopril, and also lisinopril, which has no sulfhydryl group in the structure, on free radicals were examined in vitro, using an ESR method. Superoxide and hydroxyl radical scavenging activities of alacepril metabolites, desacetylalacepril and captopril, were observed, whereas lisinopril hardly scavenged the superoxide or the hydroxyl radicals. Alacepril and its metabolites did not scavenge nitric oxide, but lisinopril showed slight scavenging activity. These findings suggest that the biological action of alacepril may be partly due to the antioxidant effect of its metabolites, having a sulfhydryl group.

摘要

阿拉普利是一种血管紧张素转换酶(ACE)抑制剂,常用于抗高血压治疗。在本研究中,使用电子自旋共振(ESR)方法在体外检测了阿拉普利及其代谢产物去乙酰阿拉普利、卡托普利,以及结构中不含巯基的赖诺普利对自由基的影响。观察到阿拉普利代谢产物去乙酰阿拉普利和卡托普利具有超氧化物和羟基自由基清除活性,而赖诺普利几乎不能清除超氧化物或羟基自由基。阿拉普利及其代谢产物不能清除一氧化氮,但赖诺普利表现出轻微的清除活性。这些发现表明,阿拉普利的生物学作用可能部分归因于其具有巯基的代谢产物的抗氧化作用。

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