Klemens S P, Sharpe C A, Cynamon M H
State University of New York Health Science Center, Syracuse 13210, USA.
Antimicrob Agents Chemother. 1996 Jan;40(1):14-6. doi: 10.1128/AAC.40.1.14.
The activity of pyrazinamide (PZA) against eight isolates of Mycobacterium tuberculosis in a murine infection model was evaluated. M. tuberculosis isolates with various degrees of in vitro susceptibility to PZA (MIC range, 32 to > 2,048 micrograms/ml) were used. Four-week-old female mice were infected intravenously with approximately 10(7) viable M. tuberculosis organisms. PZA at 150 mg/kg of body weight was started 1 day postinfection and given 5 days/week for 4 weeks. Infected but untreated mice were compared with PZA-treated mice. Mice were sacrificed at the completion of the treatment period, and viable cell counts were determined from homogenates of spleens and right lungs. PZA had activity in the murine test system against M. tuberculosis isolates for which the MICs were < or = 256 micrograms/ml. However, there was an inconsistent correlation between the absolute MICs and the reductions in organ viable cell counts. Studies with drug-resistant M. tuberculosis isolates with an isogenic background would improve evaluation of drug efficacy in the murine test system. Further evaluation of antimycobacterial agents against monodrug-resistant isolates will provide data that will be useful for development of algorithms for treatment of infection with drug-resistant organisms.
评估了吡嗪酰胺(PZA)在小鼠感染模型中对8株结核分枝杆菌的活性。使用了对PZA具有不同程度体外敏感性的结核分枝杆菌分离株(MIC范围为32至>2048微克/毫升)。4周龄雌性小鼠静脉注射约10^7个活的结核分枝杆菌。感染后1天开始给予150毫克/千克体重的PZA,每周给药5天,共4周。将感染但未治疗的小鼠与接受PZA治疗的小鼠进行比较。在治疗期结束时处死小鼠,并从脾脏和右肺匀浆中测定活细胞计数。PZA在小鼠试验系统中对MIC≤256微克/毫升的结核分枝杆菌分离株具有活性。然而,绝对MIC与器官活细胞计数减少之间的相关性并不一致。对具有同基因背景的耐多药结核分枝杆菌分离株进行研究将改善在小鼠试验系统中对药物疗效的评估。针对单药耐药分离株进一步评估抗分枝杆菌药物将提供有助于制定耐药菌感染治疗算法的数据。