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儿茶酚胺和吲哚烷基胺的杀锥虫作用

Trypanocidal effects of catecholamines and indolealkylamines.

作者信息

Owolabi O A, Wilson C, Molyneux D H, Pentreath V W

机构信息

Department of Biological Sciences, University of Salford, U.K.

出版信息

Ann Trop Med Parasitol. 1990 Apr;84(2):127-31. doi: 10.1080/00034983.1990.11812445.

Abstract

Catecholamines, indolealkylamines and their analogues are oxidized at neutral or alkaline pH, producing hydrogen peroxide, quinones and free radicals. Several of these amines were tested for trypanocidal effects on Trypanosoma brucei, which possess a well-documented vulnerability to such oxidation products. Dopamine, 5-hydroxydopamine (5-OHDA), 6-hydroxydopamine (6-OHDA), 5-hydroxytryptamine (5-HT), 5,6-dihydroxytryptamine (5,6-DHT) and 5,7-dihydroxytryptamine (5,7-DHT) killed the parasites in vitro, using a fibroblast feeder layer cell culture system, in four to 48 hours at concentrations of 10(-5)-10(-7) M. The 5-OHDA, 6-OHDA, 5,6-DHT and 5,7-DHT were also effective in vivo when tested by intraperitoneal injection of infected mice.

摘要

儿茶酚胺、吲哚烷基胺及其类似物在中性或碱性pH值下会被氧化,产生过氧化氢、醌类和自由基。对其中几种胺类化合物进行了测试,以观察其对布氏锥虫的杀锥虫作用,布氏锥虫对这类氧化产物的易感性已有充分记录。多巴胺、5-羟基多巴胺(5-OHDA)、6-羟基多巴胺(6-OHDA)、5-羟色胺(5-HT)、5,6-二羟色胺(5,6-DHT)和5,7-二羟色胺(5,7-DHT)在体外使用成纤维细胞饲养层细胞培养系统,在浓度为10(-5)-10(-7) M的情况下,四至48小时内杀死了寄生虫。通过对感染小鼠进行腹腔注射测试,5-OHDA、6-OHDA、5,6-DHT和5,7-DHT在体内也有效。

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