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在免疫抑制大鼠中比较巴龙霉素与其他氨基糖苷类药物及阿奇霉素的抗隐孢子虫活性。

A comparison of anticryptosporidial activity of paromomycin with that of other aminoglycosides and azithromycin in immunosuppressed rats.

作者信息

Rehg J E

机构信息

Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee 38101.

出版信息

J Infect Dis. 1994 Oct;170(4):934-8. doi: 10.1093/infdis/170.4.934.

Abstract

Of six evaluated aminoglycosides, paromomycin was the only one that showed activity against Cryptosporidium parvum in immunosuppressed rats. Oral dosages > or = 200 mg/kg/day reduced the severity of ileal infections; however, paromomycin was ineffective against cecal and biliary tract infections at 400 mg/kg/day orally and 50 mg/kg/day intraperitoneally. Oral paromomycin (400 mg/kg/day) was also less effective than azithromycin (400 mg/kg/day) against Cryptosporidium infection involving the ileum, cecum, or biliary tract of immunosuppressed rats. The data suggest that paromomycin may be an effective treatment for acute cryptosporidiosis of the small intestine but is probably ineffective against large intestine or biliary tract infections in the immunosuppressed host.

摘要

在评估的六种氨基糖苷类药物中,巴龙霉素是唯一一种在免疫抑制大鼠中对微小隐孢子虫显示出活性的药物。口服剂量≥200mg/kg/天可减轻回肠感染的严重程度;然而,巴龙霉素在口服400mg/kg/天和腹腔注射50mg/kg/天时,对盲肠和胆道感染无效。口服巴龙霉素(400mg/kg/天)对免疫抑制大鼠回肠、盲肠或胆道的隐孢子虫感染的疗效也低于阿奇霉素(400mg/kg/天)。数据表明,巴龙霉素可能是治疗急性小肠隐孢子虫病的有效药物,但对免疫抑制宿主的大肠或胆道感染可能无效。

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