Lenaerts Anne J, Gruppo Veronica, Marietta Karen S, Johnson Christine M, Driscoll Diane K, Tompkins Nicholas M, Rose Jerry D, Reynolds Robert C, Orme Ian M
Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO 80523, USA.
Antimicrob Agents Chemother. 2005 Jun;49(6):2294-301. doi: 10.1128/AAC.49.6.2294-2301.2005.
This study extends earlier reports regarding the in vitro and in vivo efficacies of the nitroimidazopyran PA-824 against Mycobacterium tuberculosis. PA-824 was tested in vitro against a broad panel of multidrug-resistant clinical isolates and was found to be highly active against all isolates (MIC<1 microg/ml). The activity of PA-824 against M. tuberculosis was also assessed grown under conditions of oxygen depletion. PA-824 showed significant activity at 2, 10, and 50 microg/ml, similar to that of metronidazole, in a dose-dependent manner. In a short-course mouse infection model, the efficacy of PA-824 at 50, 100, and 300 mg/kg of body weight formulated in methylcellulose or cyclodextrin/lecithin after nine oral treatments was compared with those of isoniazid, rifampin, and moxifloxacin. PA-824 at 100 mg/kg in cyclodextrin/lecithin was as active as moxifloxacin at 100 mg/kg and isoniazid at 25 mg/kg and was slightly more active than rifampin at 20 mg/kg. Long-term treatment with PA-824 at 100 mg/kg in cyclodextrin/lecithin reduced the bacterial load below 500 CFU in the lungs and spleen. No significant differences in activity between PA-824 and the other single drug treatments tested (isoniazid at 25 mg/kg, rifampin at 10 mg/kg, gatifloxacin at 100 mg/kg, and moxifloxacin at 100 mg/kg) could be observed. In summary, its good activity in in vivo models, as well as its activity against multidrug-resistant M. tuberculosis and against M. tuberculosis isolates in a potentially latent state, makes PA-824 an attractive drug candidate for the therapy of tuberculosis. These data indicate that there is significant potential for effective oral delivery of PA-824 for the treatment of tuberculosis.
本研究扩展了关于硝基咪唑并吡喃PA - 824对结核分枝杆菌的体外和体内疗效的早期报道。PA - 824在体外针对一系列广泛的耐多药临床分离株进行了测试,发现其对所有分离株均具有高活性(最低抑菌浓度<1微克/毫升)。还评估了PA - 824在缺氧条件下生长的结核分枝杆菌上的活性。PA - 824在2、10和50微克/毫升时表现出显著活性,与甲硝唑相似,呈剂量依赖性。在一个短期小鼠感染模型中,将以甲基纤维素或环糊精/卵磷脂配制的50、100和300毫克/千克体重的PA - 824经九次口服给药后的疗效与异烟肼、利福平及莫西沙星的疗效进行了比较。环糊精/卵磷脂中100毫克/千克的PA - 824与100毫克/千克的莫西沙星及25毫克/千克的异烟肼活性相当,且比20毫克/千克的利福平活性略高。环糊精/卵磷脂中100毫克/千克的PA - 824长期治疗可使肺部和脾脏中的细菌载量降至500 CFU以下。未观察到PA - 824与其他测试的单一药物治疗(25毫克/千克的异烟肼、10毫克/千克的利福平、100毫克/千克的加替沙星和100毫克/千克的莫西沙星)之间在活性上有显著差异。总之,PA - 824在体内模型中的良好活性,以及其对耐多药结核分枝杆菌和潜在潜伏状态结核分枝杆菌分离株的活性,使其成为治疗结核病的有吸引力的候选药物。这些数据表明,PA - 824经口服有效治疗结核病具有很大潜力。