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加兰他敏在体外和体内对人乙酰胆碱酯酶的选择性抑制作用。

Selective inhibition of human acetylcholinesterase by galanthamine in vitro and in vivo.

作者信息

Thomsen T, Kewitz H

机构信息

Institute of Clinical Pharmacology, Free University of Berlin, Klinikum Steglitz.

出版信息

Life Sci. 1990;46(21):1553-8. doi: 10.1016/0024-3205(90)90429-u.

Abstract

We investigated the inhibition of human cholinesterases by galanthamine, an alkaloid of the common snowdrop (galanthus nivalis). In vitro, the compound showed potent enzyme inhibition and 50-fold selectivity for acetylcholinesterase (EC 3.1.1.7) as opposed to butyrylcholinesterase (EC 3.1.1.8). There was no difference between enzyme inhibition by galanthamine in whole blood and separated fractions of plasma and erythrocytes. We conclude that galanthamine does not accumulate in large amounts in red blood cells. In vivo, administration of galanthamine in a healthy volunteer and in a patient who underwent long-term treatment confirmed the selectivity of galanthamine for acetylcholinesterase.

摘要

我们研究了加兰他敏(一种常见雪花莲(雪滴花)的生物碱)对人胆碱酯酶的抑制作用。在体外,该化合物表现出强大的酶抑制作用,对乙酰胆碱酯酶(EC 3.1.1.7)的选择性比对丁酰胆碱酯酶(EC 3.1.1.8)高50倍。加兰他敏对全血、血浆分离组分和红细胞的酶抑制作用没有差异。我们得出结论,加兰他敏不会在红细胞中大量蓄积。在体内,对一名健康志愿者和一名接受长期治疗的患者给予加兰他敏,证实了加兰他敏对乙酰胆碱酯酶的选择性。

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