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用贝纳诺霉素A(ME1451)成功治疗小鼠卡氏肺孢子虫肺炎。

Successful treatment of Pneumocystis carinii Pneumonia in mice with benanomicin A (ME1451).

作者信息

Yasuoka A, Oka S, Komuro K, Shimizu H, Kitada K, Nakamura Y, Shibahara S, Takeuchi T, Kondo S, Shimada K

机构信息

Department of Infectious Diseases, University of Tokyo, Japan.

出版信息

Antimicrob Agents Chemother. 1995 Mar;39(3):720-4. doi: 10.1128/AAC.39.3.720.

Abstract

Benanomicin A (BNM-A) has antimycotic activities via binding to mannan in the cell walls of fungi. Anti-Pneumocystis carinii activity of the agent was examined in the P. carinii-infected BALB/c nu/nu female mouse model because P. carinii also possesses mannan in the membranes. The infected mice were treated with intraperitoneal injections of six doses of BNM-A (1, 2.5, 5, 10, 30, and 100 mg/kg of body weight), 4 mg of pentamidine isethionate per kg, 100 mg of sulfamethoxazole per kg combined with 20 mg of trimethoprim per kg (co-trimoxazole), or saline for 21 days. Each dosage group consisted of 10 mice. During treatment, five mice in the control group (saline) died, whereas 8 to 10 mice in all treatment groups survived. Almost the same efficacies were obtained for the groups treated with 5 mg or more and 10 mg or more of BNM-A per kg regarding the weight and number, respectively, of cysts found in the lungs as were obtained for the groups treated with pentamidine isethionate and co-trimoxazole. Overall, a dose of 10 mg of BNM-A per kg was effective against P. carinii pneumonia infection in the mice. Thus, BNM-A is a good candidate for a novel treatment for P. carinii pneumonia as a compound with a new mechanism of action against P. carinii.

摘要

贝纳诺霉素A(BNM-A)通过与真菌细胞壁中的甘露聚糖结合而具有抗真菌活性。由于卡氏肺孢子虫的细胞膜中也含有甘露聚糖,因此在卡氏肺孢子虫感染的BALB/c裸鼠雌性小鼠模型中检测了该药物对卡氏肺孢子虫的活性。给感染的小鼠腹腔注射六剂BNM-A(1、2.5、5、10、30和100mg/kg体重)、每千克4mg的乙磺酸盐喷他脒、每千克100mg的磺胺甲恶唑与每千克20mg的甲氧苄啶(复方新诺明)或生理盐水,持续21天。每个剂量组由10只小鼠组成。治疗期间,对照组(生理盐水)有5只小鼠死亡,而所有治疗组有8至10只小鼠存活。就肺部发现的囊肿的重量和数量而言,每千克使用5mg或更多BNM-A以及每千克使用10mg或更多BNM-A治疗的组分别与使用乙磺酸盐喷他脒和复方新诺明治疗的组获得了几乎相同的疗效。总体而言,每千克10mg的BNM-A剂量对小鼠的卡氏肺孢子虫肺炎感染有效。因此,作为一种对卡氏肺孢子虫具有新作用机制的化合物,BNM-A是卡氏肺孢子虫肺炎新治疗方法的良好候选药物。

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