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Sch 29482在实验性梅毒中的评估以及与苄星青霉素G在播散性疾病和局部感染中的比较。

Evaluation of Sch 29482 in experimental syphilis and comparison with penicillin G benzathine in disseminated disease and localized infection.

作者信息

Baughn R E, Adams C, Musher D M

出版信息

Antimicrob Agents Chemother. 1984 Sep;26(3):401-4. doi: 10.1128/AAC.26.3.401.

Abstract

The present study was designed to assess the in vivo activity of Sch 29482, a new penem antibiotic, against disseminated and localized Treponema pallidum infections in rabbits. Animals were inoculated either intravenously or intradermally. Randomized groups then received 25 or 50 mg of Sch 29482 per kilogram of body weight twice a day for 7 days, two weekly injections of 200,000 U of penicillin G benzathine for comparative purposes, or no antibiotic therapy. In both infection models, striking differences were noted between the untreated control rabbits and rabbits receiving penicillin G benzathine or high-dose Sch 29482. Intravenously infected rabbits did not develop disseminated lesions or orchitis, and chancres produced by intradermal infection regressed and healed rapidly after both treatment regimens. Infectivity studies also suggested that high-dose Sch 29482 and penicillin G benzathine were effective since the testes and lymph nodes of treated animals were free of infectious organisms. Treatment of animals with the lower dose of Sch 29482 represented borderline or suboptimal therapy, with a failure rate of one in four for each infection model.

摘要

本研究旨在评估新型青霉烯抗生素Sch 29482对兔播散性和局限性梅毒螺旋体感染的体内活性。动物通过静脉注射或皮内注射接种。然后将随机分组的动物每天两次按每千克体重25或50毫克给予Sch 29482,持续7天;为作比较,每两周注射一次20万单位苄星青霉素G;或不进行抗生素治疗。在两种感染模型中,未治疗的对照兔与接受苄星青霉素G或高剂量Sch 29482的兔之间均存在显著差异。静脉感染的兔未出现播散性病变或睾丸炎,皮内感染产生的溃疡在两种治疗方案后均迅速消退并愈合。感染性研究还表明,高剂量Sch 29482和苄星青霉素G是有效的,因为治疗动物的睾丸和淋巴结中没有感染性生物体。用较低剂量Sch 29482治疗动物代表临界或次优治疗,每种感染模型的失败率为四分之一。

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Azithromycin versus penicillin G benzathine for early syphilis.阿奇霉素与苄星青霉素治疗早期梅毒的比较
Cochrane Database Syst Rev. 2012 Jun 13;2012(6):CD007270. doi: 10.1002/14651858.CD007270.pub2.

本文引用的文献

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Sch 29482: in-vitro antibacterial activity and susceptibility to beta-lactamases.
J Antimicrob Chemother. 1982 Feb;9 Suppl C:25-30. doi: 10.1093/jac/9.suppl_c.25.
8

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