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Use of normal C57BL/6 mice with established Mycobacterium avium infections as an alternative model for evaluation of antibiotic activity.

机译:使用已建立的鸟分枝杆菌感染的正常C57BL / 6小鼠作为评估抗生素活性的替代模型。

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摘要

Several murine models have been used to evaluate the activities of antimicrobial agents against Mycobacterium avium infection. The main model used is the beige mouse model, but beige mice are expensive and not easily available. Thus, we developed a model of infection in wild C57BL/6 mice. The drugs that exhibited some activity in a previous model of early infection were evaluated in a new model of established infection. Sparfloxacin (50 mg/kg of body weight), ethambutol (50 mg/kg), minocycline (25 mg/kg), and the inhibitor of the cortisol receptors RU-40555 (100 mg/kg) were compared with clarithromycin (50 mg/kg). Treatments were started 5 weeks after the inoculation and were continued for 21 days. Sparfloxacin and RU-40555, which exhibited a moderate activity in the model of early infection, were not effective in this model of established infection. Clarithromycin and combinations with clarithromycin kept their activities against M. avium infection, both in the spleen and in lungs. The present model of established infection of normal C57BL/6 mice is more relevant than the model of early infection for a stringent evaluation of drugs.
机译:几种鼠模型已经用于评估抗鸟分枝杆菌感染的抗菌剂的活性。所使用的主要模型是米色鼠标模型,但是米色鼠标价格昂贵且不易获得。因此,我们建立了野生C57BL / 6小鼠感染的模型。在建立的新感染模型中评估了在先前的早期感染模型中表现出一定活性的药物。将司帕沙星(50 mg / kg体重),乙胺丁醇(50 mg / kg),米诺环素(25 mg / kg)和皮质醇受体RU-40555抑制剂(100 mg / kg)与克拉霉素(50 mg /公斤)。接种后5周开始治疗,并持续21天。在早期感染模型中表现出中等活性的司帕沙星和RU-40555在这种已建立的感染模型中无效。克拉霉素及其与克拉霉素的组合在脾脏和肺部均保持了抗鸟分枝杆菌感染的活性。对于严格的药物评估,目前建立的正常C57BL / 6小鼠感染模型比早期感染模型更相关。

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