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恶性疟原虫“体外”超微结构。II. 不同喹啉作用的形态学模式。

Ultrastructure of Plasmodium falciparum "in vitro". II. Morphological patterns of different quinolines effects.

作者信息

Olliaro P, Castelli F, Caligaris S, Druilhe P, Carosi G

机构信息

Department of Infectious Diseases, University of Pavia, Italy.

出版信息

Microbiologica. 1989 Jan;12(1):15-28.

PMID:2654570
Abstract

In the present morphological study, we used electron microscopy (EM) to evaluate the activity of three quinolines upon Plasmodium falciparum strains cultured in vitro. The drugs (namely chloroquine, mefloquine and a new active substance, SF6606) showed common cellular targets (i.e. feeding process, protein synthesis, membrane formation and utilisation) but gave rise to different morphological features. EM as a tool is able to reveal a variety of drug-induced alterations, but it does not seem to supply evidence of a definite mechanism of action. Nevertheless, our observations suggest that each drug acts via several mechanisms, possibly linked to different degrees of parasite susceptibility.

摘要

在目前的形态学研究中,我们使用电子显微镜(EM)来评估三种喹啉对体外培养的恶性疟原虫菌株的活性。这些药物(即氯喹、甲氟喹和一种新的活性物质SF6606)显示出共同的细胞靶点(即摄食过程、蛋白质合成、膜形成和利用),但产生了不同的形态特征。电子显微镜作为一种工具能够揭示各种药物诱导的变化,但似乎并未提供明确作用机制的证据。然而,我们的观察结果表明,每种药物都通过几种机制起作用,可能与寄生虫不同程度的易感性有关。

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