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铜绿假单胞菌在体外单次及多次接触氨基糖苷类药物后的抗生素后效应

Postantibiotic effect in Pseudomonas aeruginosa following single and multiple aminoglycoside exposures in vitro.

作者信息

Karlowsky J A, Zhanel G G, Davidson R J, Hoban D J

机构信息

Department of Medical Microbiology, University of Manitoba, Winnipeg, Canada.

出版信息

J Antimicrob Chemother. 1994 May;33(5):937-47. doi: 10.1093/jac/33.5.937.

Abstract

The effect of single and multiple 2-h aminoglycoside exposures on the duration of the postantibiotic effect (PAE) and bacterial killing were investigated using a reference strain (ATCC 27853) and four clinical isolates of Pseudomonas aeruginosa. Concentration-dependent PAE and bacterial killing were demonstrated following single exposures to amikacin, gentamicin or tobramycin. Cultures were also repeatedly exposed to peak aminoglycoside concentration simulating traditional (three times a day) and once daily dosing regimens. Aminoglycoside re-exposures every 8 h at the original culture MIC produced significant, successive reductions in PAE (P < 0.05) and bacterial killing (P < 0.01) coincident with increases in culture MICs. Identical experiments re-exposing cultures to their predetermined, induced MICs demonstrated similar to significantly longer PAEs (P < 0.05) than those observed following first exposure. Multiple gentamicin or tobramycin exposures at 8 mg/L (traditional peak) every 8 h or 24 mg/L (once daily peak) once every 24 h both showed significant reductions in PAE (P < 0.05) and bacterial killing (P < 0.05) on repeated dosing. However, the once-daily high peak concentration exposure demonstrated significantly longer PAEs and greater bacterial killing both initially and upon re-exposure compared with the 8-hourly exposure. In addition, the once daily dosing regimen maintained substantially larger aminoglycoside concentration/MIC ratios. We conclude that multiple exposure of P. aeruginosa in-vitro, to aminoglycosides at the intervals tested, reduces the PAE and bacterial killing and increases the MICs.

摘要

使用参考菌株(ATCC 27853)和4株铜绿假单胞菌临床分离株,研究了单次和多次2小时氨基糖苷类药物暴露对抗生素后效应(PAE)持续时间和细菌杀伤作用的影响。单次暴露于阿米卡星、庆大霉素或妥布霉素后,呈现出浓度依赖性的PAE和细菌杀伤作用。培养物还反复暴露于模拟传统(每日3次)和每日1次给药方案的氨基糖苷类药物峰值浓度。每8小时在原始培养物最低抑菌浓度(MIC)下重新暴露氨基糖苷类药物,会导致PAE(P < 0.05)和细菌杀伤作用(P < 0.01)显著且连续降低,同时培养物MIC升高。将培养物重新暴露于其预先确定的诱导MIC的相同实验表明,与首次暴露后观察到的情况相比,PAE显著延长(P < 0.05)。每8小时以8 mg/L(传统峰值)或每24小时以24 mg/L(每日1次峰值)多次暴露庆大霉素或妥布霉素,在重复给药时均显示PAE(P < 0.05)和细菌杀伤作用(P < 0.05)显著降低。然而,与每8小时暴露相比,每日1次的高峰值浓度暴露在初始和重新暴露时均显示出显著更长的PAE和更强的细菌杀伤作用。此外,每日1次给药方案维持了实质上更大的氨基糖苷类药物浓度/MIC比值。我们得出结论,体外多次以测试的间隔时间将铜绿假单胞菌暴露于氨基糖苷类药物会降低PAE和细菌杀伤作用,并增加MIC。

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