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体外培养对布氏布氏锥虫对二脒那嗪、异美汀、喹啉嘧啶胺和美拉胂醇耐药稳定性的影响。

Effect of in vitro cultivation on the stability of resistance of Trypanosoma brucei brucei to diminazene, isometamidium, quinapyramine, and Mel B.

作者信息

Kaminsky R, Zweygarth E

机构信息

International Laboratory for Research on Animal Diseases, Nairobi, Kenya.

出版信息

J Parasitol. 1989 Feb;75(1):42-5.

PMID:2918443
Abstract

A Trypanosoma brucei brucei stock resistant to diminazene aceturate, isometamidium chloride, quinapyramine sulfate, and Mel B was grown in vitro and its response to these drugs compared to that of a drug-sensitive trypanosome stock. There was little if any change of drug sensitivity after in vitro propagation as bloodstream forms for 120, 177, and 275 days and after in vitro transformation of bloodstream forms into procyclic, epimastigote, and finally metacyclic forms. Drug resistance was stable during in vitro maintenance in the absence of drugs in both culture systems. The response of resistant and sensitive T. b. brucei to diminazene in vitro correlated with their sensitivity pattern in vivo. Thus, in vitro techniques can be used to study drug resistance in trypanosomes.

摘要

一株对乙酰甘氨酸二脒那嗪、氯异美啶、硫酸喹啉嘧啶和美拉胂醇耐药的布氏布氏锥虫原种在体外培养,将其对这些药物的反应与药物敏感的锥虫原种进行比较。作为血流形式在体外繁殖120、177和275天以及血流形式在体外转化为前循环型、上鞭毛体型并最终转化为循环后期型后,药物敏感性几乎没有变化(如果有变化的话)。在两种培养系统中,在无药物的体外维持期间,耐药性是稳定的。耐药和敏感的布氏布氏锥虫在体外对二脒那嗪的反应与其在体内的敏感性模式相关。因此,体外技术可用于研究锥虫的耐药性。

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