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曼氏血吸虫:5-羟色胺摄取及其药物抑制作用

Schistosoma mansoni: serotonin uptake and its drug inhibition.

作者信息

Wood P J, Mansour T E

出版信息

Exp Parasitol. 1986 Aug;62(1):114-9. doi: 10.1016/0014-4894(86)90014-7.

Abstract

5-Hydroxytryptamine (serotonin) uptake by male and female Schistosoma mansoni was studied in vitro. Initial uptake was determined during the first 2 min of incubation with the indoleamine. There were two types of uptake: a saturable component that is apparent at low concentrations of serotonin, and a passive component that predominates at high concentrations. Female S. mansoni take up more 5-hydroxytryptamine per milligram protein than do the males. Studies on the distribution of 5-hydroxytryptamine taken up by the parasites show that a large proportion of the indoleamine is in the tegument. The female tegument had a greater proportion of the 5-hydroxytryptamine taken up than did the male tegument. The evidence indicated that 5-hydroxytryptamine associated with tegument represented the passive uptake while uptake in the main parasite body was both active and passive. Compounds that were shown to inhibit 5-hydroxytryptamine uptake include methylclonazepam, metergoline, imipramine, and ouabain. Maximal inhibition by these compounds ranged from 50 to 60%. Inhibition appeared to be confined to the saturable uptake component of the body fraction.

摘要

对曼氏血吸虫雌雄虫体摄取5-羟色胺(血清素)进行了体外研究。在与吲哚胺孵育的最初2分钟内测定初始摄取量。摄取有两种类型:一种是在低浓度血清素时明显的可饱和成分,另一种是在高浓度时占主导的被动成分。每毫克蛋白质中,雌性曼氏血吸虫摄取的5-羟色胺比雄性更多。对寄生虫摄取的5-羟色胺分布的研究表明,很大一部分吲哚胺存在于体表。雌性体表摄取的5-羟色胺比例比雄性体表更大。证据表明,与体表相关的5-羟色胺代表被动摄取,而在虫体主要部分的摄取既有主动摄取也有被动摄取。已证明能抑制5-羟色胺摄取的化合物包括甲基氯硝西泮、美替拉酮、丙咪嗪和哇巴因。这些化合物的最大抑制率在50%至60%之间。抑制作用似乎仅限于虫体部分的可饱和摄取成分。

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