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新型羟基萘醌566C80对大鼠伯氏疟原虫感染的因果预防活性。

The causal prophylactic activity of the novel hydroxynaphthoquinone 566C80 against Plasmodium berghei infections in rats.

作者信息

Davies C S, Pudney M, Matthews P J, Sinden R E

出版信息

Acta Leiden. 1989;58(2):115-28.

PMID:2489391
Abstract

The influence of the novel hydroxynaphthoquinone 566C80 on exoerythrocytic development of Plasmodium berghei was examined in Brown Norway rats. The procedure employed was designed to identify residual activity of the drug against tissue merozoites emerging into the bloodstream and to distinguish this from any observed causal prophylactic activity against the liver stages. Single oral doses of 10 and 1 mg/kg of 566C80 administered 3 hours after sporozoite-inoculation were effective in preventing the appearance of a patent parasitaemia, while a dose of 0.1 mg/kg significantly reduced the severity of the ensuing blood infection. There was a pronounced residual effect of 566C80 against the blood forms at a dose of 10 mg/kg, a slight residual effect at a dose of 1 mg/kg, but no apparent residual effect at 0.1 mg/kg. At the time when EE merozoites would normally emerge into the bloodstream, an aliquot of blood was sub-inoculated into mice from sporozoite-infected, 566C80-treated rats. This procedure confirmed that 566C80 is active against the exoerythrocytic stages of Plasmodium berghei.

摘要

在棕色挪威大鼠中研究了新型羟基萘醌566C80对伯氏疟原虫红细胞外期发育的影响。所采用的程序旨在确定该药物对进入血流的组织裂殖子的残留活性,并将其与观察到的对肝期的任何因果预防活性区分开来。在接种子孢子3小时后口服单剂量10和1mg/kg的566C80可有效预防明显的寄生虫血症出现,而0.1mg/kg的剂量可显著降低随后血液感染的严重程度。566C80在10mg/kg剂量时对血液形态有明显的残留作用,在1mg/kg剂量时有轻微残留作用,但在0.1mg/kg时无明显残留作用。在红细胞外期裂殖子正常进入血流时,将一份血液从小孢子感染、566C80处理的大鼠中接种到小鼠体内。该程序证实566C80对伯氏疟原虫的红细胞外期有活性。

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