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β-内酰胺类药物对大肠杆菌的迟滞期和杀菌期的同步药效学分析

Simultaneous pharmacodynamic analysis of the lag and bactericidal phases exhibited by beta-lactams against Escherichia coli.

作者信息

Li R C

机构信息

Department of Pharmacy, Faculty of Medicine, The Chinese University of Hong Kong.

出版信息

Antimicrob Agents Chemother. 1996 Oct;40(10):2306-10. doi: 10.1128/AAC.40.10.2306.

Abstract

Antibiotic-bacterium interactions are complex in nature. In many cases, bacterial killing does not commence immediately after the addition of an antibiotic, and a lag period is observed. Antibiotic permeation and/or the intermediate steps that exist between antibiotic-receptor binding and expression of cell death are two major possible causes for such lag period. This study was primarily designed to determine the relationship, if any, between antibiotic concentrations and the lag periods by a modeling approach. Short-term time-kill studies were conducted for amoxicillin, ampicillin, penicillin-G, oxacillin, and dicloxacillin against Escherichia coli. In conjunction with the use of a saturable rate model to describe the concentration-dependent killing process, a first-order induction (initiation) rate constant was used to characterize the delay in bacterial killing during the lag period. For all of the beta-lactams tested, parameters describing the bactericidal effect suggest that amoxicillin and ampicillin were much more potent than oxacillin and dicloxacillin. The induction rate constant estimates for both ampicillin and amoxicillin were found to relate linearly to concentrations. Nevertheless, these induction rate constant estimates were lower for penicillin-G, oxacillin, and dicloxacillin and increased nonlinearly with concentrations until an apparent plateau was observed. These findings support the hypothesis that the permeation process is potentially a rate-limiting step for the rapid bactericidal beta-lactams such as ampicillin and amoxicillin. However, as suggested by previous observations of the various morphological changes induced by beta-lactams, the contribution of the steps following antibiotic-receptor complex formation to the lag period might be significant for the less bactericidal antibiotics such as oxacillin and dicloxacillin. Findings from the present modeling approach can potentially be used to guide future bench experimentation.

摘要

抗生素与细菌的相互作用本质上很复杂。在许多情况下,添加抗生素后细菌不会立即被杀死,而是会观察到一个延迟期。抗生素渗透和/或抗生素与受体结合及细胞死亡表达之间存在的中间步骤是导致这种延迟期的两个主要可能原因。本研究主要旨在通过建模方法确定抗生素浓度与延迟期之间是否存在关系。针对阿莫西林、氨苄西林、青霉素G、苯唑西林和双氯西林对大肠杆菌进行了短期时间杀灭研究。结合使用饱和速率模型来描述浓度依赖性杀灭过程,采用一级诱导(起始)速率常数来表征延迟期内细菌杀灭的延迟情况。对于所有测试的β-内酰胺类抗生素,描述杀菌效果的参数表明阿莫西林和氨苄西林比苯唑西林和双氯西林的杀菌能力强得多。发现氨苄西林和阿莫西林的诱导速率常数估计值与浓度呈线性关系。然而,青霉素G、苯唑西林和双氯西林的这些诱导速率常数估计值较低,并且随着浓度呈非线性增加,直至观察到明显的平台期。这些发现支持了这样的假设,即渗透过程可能是氨苄西林和阿莫西林等快速杀菌β-内酰胺类抗生素的限速步骤。然而,正如先前对β-内酰胺类抗生素诱导的各种形态变化的观察所表明的那样,对于杀菌能力较弱的抗生素如苯唑西林和双氯西林,抗生素-受体复合物形成后的步骤对延迟期的贡献可能很大。本建模方法的研究结果有可能用于指导未来的实验室实验。

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