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卡氏肺孢子虫:用于研究大鼠(褐家鼠属)卡氏肺孢子虫肺炎治疗或预防药物疗效的改良模型。

Pneumocystis carinii: improved models to study efficacy of drugs for treatment or prophylaxis of Pneumocystis pneumonia in the rat (Rattus spp.).

作者信息

Bartlett M S, Fishman J A, Durkin M M, Queener S F, Smith J W

机构信息

Indiana University School of Medicine, Indianapolis 46223.

出版信息

Exp Parasitol. 1990 Jan;70(1):100-6. doi: 10.1016/0014-4894(90)90089-u.

Abstract

Rats which were immunosuppressed with adrenal corticosteroids then transtracheally inoculated with Pneumocystis carinii were evaluated as models for study of drug efficacy. Trimethoprim/sulfamethoxazole, known to be effective against Pneumocystis, was given in therapeutic and prophylactic regimens and its long-term effectiveness determined by a protocol to study relapse. Untreated animals uniformly developed severe infection with differences in numbers of organisms between untreated and treated animals being greater than two logs. Therapy of prophylaxis studies could be completed in 6 to 7 weeks. Animals given prophylaxis or therapy with trimethoprim/sulfamethoxazole had few organisms detected in lungs. Numbers of organisms did not increase during the 4 weeks when the animals were continued on immunosuppression after discontinuing treatment as long as reinfection was prevented. These models are useful for evaluating anti-Pneumocystis activity of antimicrobials. Relapse study data suggest that reinfection may have an important role in development of recurrent Pneumocystis pneumonia.

摘要

先用肾上腺皮质类固醇进行免疫抑制,然后经气管接种卡氏肺孢子虫的大鼠被评估为研究药物疗效的模型。已知对卡氏肺孢子虫有效的甲氧苄啶/磺胺甲恶唑以治疗和预防方案给药,其长期有效性通过研究复发的方案来确定。未经治疗的动物均出现严重感染,未经治疗和治疗动物之间的病原体数量差异大于两个对数。预防研究的治疗可在6至7周内完成。用甲氧苄啶/磺胺甲恶唑进行预防或治疗的动物肺部检测到的病原体很少。在停止治疗后继续进行免疫抑制的4周内,只要防止再次感染,病原体数量就不会增加。这些模型对于评估抗微生物药物的抗肺孢子虫活性很有用。复发研究数据表明,再次感染可能在复发性肺孢子虫肺炎的发生中起重要作用。

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