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抗精神病吩噻嗪类药物对布氏锥虫的杀锥虫作用。

Trypanocidal action of neuroleptic phenothiazines in Trypanosoma brucei.

作者信息

Seebeck T, Gehr P

出版信息

Mol Biochem Parasitol. 1983 Nov;9(3):197-208. doi: 10.1016/0166-6851(83)90097-x.

Abstract

This paper reports the effects of a series of phenothiazine derivatives on trypanosomes in vitro. Our results demonstrate that trypanosomes are very sensitive to some of these compounds at micromolar concentrations. Electron microscopic analysis of drug-treated cells shows that the pellicular layer of microtubules is selectively disintegrated by phenothiazine treatment, while the flagellar axoneme is entirely resistant to the drug. These observations suggest that phenothiazines might constitute a promising candidate group for the development of new trypanocidal drugs. Furthermore, they indicate that the mechanism of drug action is mediated through a specific interaction of phenothiazines with the pellicular, but not with the flagellar, microtubules.

摘要

本文报道了一系列吩噻嗪衍生物在体外对锥虫的作用。我们的结果表明,锥虫对其中一些化合物在微摩尔浓度下非常敏感。对药物处理细胞的电子显微镜分析表明,吩噻嗪处理可使微管的表膜层选择性解体,而鞭毛轴丝对该药物完全耐药。这些观察结果表明,吩噻嗪可能是开发新型杀锥虫药物的一个有前景的候选药物组。此外,它们表明药物作用机制是通过吩噻嗪与表膜微管而非鞭毛微管的特异性相互作用介导的。

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