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药物对克氏锥虫及其与心肌细胞“体外”相互作用的影响。

Effect of drugs on Trypanosoma cruzi and on its interaction with heart muscle cell "in vitro".

作者信息

de Castro S L, de Meirelles M de N

机构信息

Instituto Oswaldo Cruz, Departamento de Ultraestrutura e Biologia Celular, Rio de Janeiro, Brasil.

出版信息

Mem Inst Oswaldo Cruz. 1987 Apr-Jun;82(2):209-18. doi: 10.1590/s0074-02761987000200009.

Abstract

Megazol, nifurtimox, benznidazol and allopurinol were investigated, by light and electron microscopy, for their action on T. cruzi. Both the direct effect upon amastigote and trypomastigote forms and the effect upon the interaction of heart muscle cells (HMC) with bloodstream trypomastigotes were studied. The proliferation of amastigotes in Warren medium was inhibited in a dose-dependent manner by megazol, nifurtimox and benznidazol. Treatment of amastigotes (25-50 microM/24 h) and trypomastigotes (25 microM/24h) led to several ultrastructural alterations in the parasites. These three drugs also had a potent effect on the treatment of infected heart muscle cells when added at the beginning of the interaction or after one or three days of infection. The interiorized parasites showed a similar pattern of ultrastructural alterations as observed by the direct effect on the amastigotes. The primary heart muscle cell culture proved to be a suitable model for the study of drugs on intracellular parasites. Likewise, the amastigote proliferation in axenic medium was shown to be an adequate assay for an initial trial of drugs. These parameters seem very reliable to us for a systematic investigation of the mechanism of action of new drugs.

摘要

通过光学显微镜和电子显微镜研究了灭滴灵、硝呋替莫、苯硝唑和别嘌呤醇对克氏锥虫的作用。研究了它们对无鞭毛体和锥鞭毛体形式的直接作用以及对心肌细胞(HMC)与血流中锥鞭毛体相互作用的影响。灭滴灵、硝呋替莫和苯硝唑以剂量依赖的方式抑制无鞭毛体在沃伦培养基中的增殖。用无鞭毛体(25-50微摩尔/24小时)和锥鞭毛体(25微摩尔/24小时)处理会导致寄生虫出现几种超微结构改变。当在相互作用开始时或感染1天或3天后添加这三种药物时,它们对感染的心肌细胞也有显著的治疗效果。内化的寄生虫表现出与对无鞭毛体直接作用时观察到的类似超微结构改变模式。原代心肌细胞培养被证明是研究药物对细胞内寄生虫作用的合适模型。同样,无鞭毛体在无菌培养基中的增殖被证明是药物初步试验的合适测定方法。对我们来说,这些参数对于系统研究新药的作用机制似乎非常可靠。

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