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HIV蛋白酶抑制剂的抗利什曼原虫活性。

Antileishmanial activity of HIV protease inhibitors.

作者信息

Savoia Dianella, Allice Tiziano, Tovo Pier-Angelo

机构信息

Laboratory of Microbiology, Department of Clinical and Biological Sciences, University of Torino at S. Luigi Gonzaga Hospital, 10043 Orbassano, Torino, Italy.

出版信息

Int J Antimicrob Agents. 2005 Jul;26(1):92-4. doi: 10.1016/j.ijantimicag.2005.04.003.

Abstract

The proteasomes of some protozoa are possible targets for chemotherapy. Leishmaniasis is a major health problem in human immunodeficiency virus (HIV) co-infected subjects. Two HIV protease inhibitors (PI), indinavir and saquinavir, have been shown to block proteasome functions; we therefore investigated their effects on the growth of two Leishmania spp. (Leishmania major and Leishmania infantum). After 24 h of treatment, both drugs exhibited a dose-dependent antileishmanial activity, with 50% lethal dose (LD50) values of, respectively, 8.3 microM and 7 microM on L. major; minor activity was observed on L. infantum. These results add new in vitro insights into the wide-spectrum efficacy of PI and suggest studying their action on amastigote forms of leishmania within macrophages in order to validate their potential contribution against opportunistic infections in treated seropositive patients.

摘要

一些原生动物的蛋白酶体可能是化疗的靶点。利什曼病是人类免疫缺陷病毒(HIV)合并感染患者的一个主要健康问题。两种HIV蛋白酶抑制剂(PI),茚地那韦和沙奎那韦,已被证明可阻断蛋白酶体功能;因此,我们研究了它们对两种利什曼原虫(硕大利什曼原虫和婴儿利什曼原虫)生长的影响。治疗24小时后,两种药物均表现出剂量依赖性抗利什曼原虫活性,对硕大利什曼原虫的半数致死剂量(LD50)值分别为8.3 microM和7 microM;对婴儿利什曼原虫观察到较小的活性。这些结果为PI的广谱疗效提供了新的体外见解,并建议研究它们对巨噬细胞内利什曼原虫无鞭毛体形式的作用,以验证它们对治疗血清阳性患者机会性感染的潜在贡献。

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