Bermudez L E, Wu M, Young L S, Inderlied C B
Kuzell Institute for Arthritis and Infectious Diseases, Medical Research Institute of San Francisco, California Pacific Medical Center.
J Infect Dis. 1992 Oct;166(4):923-6. doi: 10.1093/infdis/166.4.923.
Postantibiotic effect (PAE) has received little attention in the therapy of chronic intracellular infections, such as those caused by mycobacteria. Amikacin is active therapeutically against Mycobacterium avium complex, even though serum levels exceed the MIC for only a few hours. To determine the PAE of amikacin and rifapentine for M. avium, bacteria were exposed to concentrations of 1x, 4x, and 10x the MIC of each drug for up to 120 min. Regrowth of M. avium was compared with similarly diluted untreated cultures. No PAE was observed on an inoculum of 10(4) bacteria when rifapentine was used at 5x MIC, although a slight inhibition of growth was obtained at 10x MIC for 2 h. For amikacin, PAE was observed up to 48 h at concentrations of 4x and 8x MIC and exposure times of 30-120 min. A PAE of 22 h was seen with 10(7) cfu of M. avium during incubation for 30 min with amikacin at 4x MIC. These results show that amikacin, unlike rifapentine, has a long PAE against M. avium.
抗生素后效应(PAE)在慢性细胞内感染(如由分枝杆菌引起的感染)的治疗中很少受到关注。阿米卡星对鸟分枝杆菌复合体具有治疗活性,尽管血清水平仅在数小时内超过最低抑菌浓度(MIC)。为了确定阿米卡星和利福喷汀对鸟分枝杆菌的PAE,将细菌暴露于每种药物MIC的1倍、4倍和10倍浓度下长达120分钟。将鸟分枝杆菌的再生长与同样稀释的未处理培养物进行比较。当利福喷汀以5倍MIC使用时,在接种10⁴个细菌时未观察到PAE,尽管在10倍MIC下2小时获得了轻微的生长抑制。对于阿米卡星,在4倍和8倍MIC浓度以及30 - 120分钟暴露时间下,PAE可持续长达48小时。在用4倍MIC的阿米卡星孵育30分钟期间,观察到10⁷cfu鸟分枝杆菌的PAE为22小时。这些结果表明,与利福喷汀不同,阿米卡星对鸟分枝杆菌具有较长的PAE。