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抗疟无性生殖阶段特异性和配子体杀伤活性的 HIV 蛋白酶抑制剂。

Antimalarial asexual stage-specific and gametocytocidal activities of HIV protease inhibitors.

机构信息

Queensland Institute of Medical Research, 300 Herston Rd., Herston, Queensland, Australia.

出版信息

Antimicrob Agents Chemother. 2010 Mar;54(3):1334-7. doi: 10.1128/AAC.01512-09. Epub 2009 Dec 22.

Abstract

The stage-specific antimalarial activities of a panel of antiretroviral protease inhibitors (PIs), including two nonpeptidic PIs (tipranavir and darunavir), were tested in vitro against Plasmodium falciparum. While darunavir demonstrated limited antimalarial activity (effective concentration [EC(50)], >50 microM), tipranavir was active at clinically relevant concentrations (EC(50), 12 to 21 microM). Saquinavir, lopinavir, and tipranavir preferentially inhibited the growth of mature asexual-stage parasites (24 h postinvasion). While all of the PIs tested inhibited gametocytogenesis, tipranavir was the only one to exhibit gametocytocidal activity.

摘要

研究人员检测了一组抗逆转录病毒蛋白酶抑制剂(PI),包括两种非肽类 PI(替拉那韦和达芦那韦)的抗疟活性,这些药物针对恶性疟原虫(Plasmodium falciparum)在体外的不同阶段进行了测试。达芦那韦显示出有限的抗疟活性(有效浓度[EC(50)],大于 50 微摩尔),而替拉那韦在临床相关浓度下具有活性(EC(50),12 至 21 微摩尔)。沙奎那韦、洛匹那韦和替拉那韦优先抑制成熟的无性期寄生虫的生长(入侵后 24 小时)。虽然所有测试的 PI 都抑制配子体形成,但只有替拉那韦表现出配子体杀伤活性。

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