新型羟基萘醌566C80对大鼠伯氏疟原虫感染的因果预防作用。

Acta Leidensia Pub Date : 1989-01-01
C S Davies, M Pudney, P J Matthews, R E Sinden
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引用次数: 0

摘要

本文研究了新型羟基萘醌566C80对褐挪威大鼠伯氏疟原虫外红细胞发育的影响。所采用的程序旨在确定药物对出现在血液中的组织分裂子的残留活性,并将其与任何观察到的针对肝脏阶段的因果预防活性区分开来。566C80单次口服剂量分别为10 mg/kg和1 mg/kg,在接种孢子虫3小时后可有效防止出现明显寄生虫血症,而0.1 mg/kg的剂量可显著降低随后血液感染的严重程度。566C80在剂量为10 mg/kg时对血液形态有明显的残留效应,在剂量为1 mg/kg时有轻微的残留效应,但在剂量为0.1 mg/kg时无明显的残留效应。在正常情况下,当EE孢子子进入血流时,从感染了566c80的大鼠中提取等量的血液亚接种到小鼠体内。这个过程证实566C80对伯氏疟原虫的外红细胞阶段有活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The causal prophylactic activity of the novel hydroxynaphthoquinone 566C80 against Plasmodium berghei infections in rats.

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.

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