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两种对刚地弓形虫具有体外和体内活性的2-羟基-3-烷基-1,4-萘醌。

Two 2-hydroxy-3-alkyl-1,4-naphthoquinones with in vitro and in vivo activities against Toxoplasma gondii.

作者信息

Khan A A, Nasr M, Araujo F G

机构信息

Department of Immunology and Infectious Diseases, Research Institute, Palo Alto Medical Foundation, Palo Alto, California 94301, USA.

出版信息

Antimicrob Agents Chemother. 1998 Sep;42(9):2284-9. doi: 10.1128/AAC.42.9.2284.

Abstract

Two 3-alkyl-substituted 2-hydroxy-1,4-naphthoquinones, NSC 113452 (NSC52) and NSC 113455 (NSC55), were evaluated for activity against Toxoplasma gondii in vitro and in murine models of acute toxoplasmosis. In vitro, both NSC52 and NSC55 significantly inhibited intracellular replication of T. gondii. In vivo, each compound was examined alone and in combination with other drugs currently used for treatment of human toxoplasmosis. Although none of the compounds protected mice against death when administered orally, both were significantly protective when administered intraperitoneally. In addition, a significant increase in survival was observed when suboptimal doses of each compound were used in combination with suboptimal doses of pyrimethamine or sulfadiazine. These results indicate that combinations of NSC52 or NSC55 with pyrimethamine or sulfadiazine have promising activity against T. gondii.

摘要

对两种3-烷基取代的2-羟基-1,4-萘醌,即NSC 113452(NSC52)和NSC 113455(NSC55),进行了体外抗刚地弓形虫活性以及在急性弓形虫病小鼠模型中的活性评估。在体外,NSC52和NSC55均能显著抑制刚地弓形虫的细胞内复制。在体内,分别对每种化合物以及与目前用于治疗人类弓形虫病的其他药物联合使用进行了研究。虽然口服给药时没有一种化合物能保护小鼠免于死亡,但腹腔注射时两种化合物均具有显著的保护作用。此外,当使用次优剂量的每种化合物与次优剂量的乙胺嘧啶或磺胺嘧啶联合使用时,观察到存活率显著提高。这些结果表明,NSC52或NSC55与乙胺嘧啶或磺胺嘧啶联合使用对刚地弓形虫具有有前景的活性。

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