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抗生素诱导的内毒素释放:美罗培南与其他抗生素的体外比较

Antibiotic-induced release of endotoxin: in-vitro comparison of meropenem and other antibiotics.

作者信息

Trautmann M, Zick R, Rukavina T, Cross A S, Marre R

机构信息

Department of Medical Microbiology and Hygiene, University of Ulm, Germany.

出版信息

J Antimicrob Chemother. 1998 Feb;41(2):163-9. doi: 10.1093/jac/41.2.163.

Abstract

The influence of meropenem, a new carbapenem antibiotic, on cell morphology and in-vitro lipopolysaccharide (LPS) release from Escherichia coli was compared with that of imipenem, ceftazidime, tobramycin and ciprofloxacin. Free and cell-associated LPS was quantified by means of a capture ELISA method based on the recognition of E. coli LPS by monoclonal antibodies. Microscopically, meropenem was found to induce spheroplast formation similar to that seen with imipenem, while ceftazidime and ciprofloxacin induced filament formation. Free and cell-associated LPS levels were low in the presence of meropenem, imipenem, ciprofloxacin and tobramycin, but high in the presence of ceftazidime. Reduced endotoxin release appears to be a common property of carbapenem antibiotics. Morphological changes in bacteria in the presence of antibiotics do not predict their LPS-liberating effect since ciprofloxacin induced low levels of LPS despite causing filament formation.

摘要

将新型碳青霉烯类抗生素美罗培南与亚胺培南、头孢他啶、妥布霉素和环丙沙星对细胞形态以及大肠杆菌体外脂多糖(LPS)释放的影响进行了比较。基于单克隆抗体对大肠杆菌LPS的识别,采用捕获ELISA法对游离型和细胞相关型LPS进行定量。在显微镜下发现,美罗培南诱导形成原生质球,类似于亚胺培南的作用,而头孢他啶和环丙沙星诱导形成丝状结构。在美罗培南、亚胺培南、环丙沙星和妥布霉素存在的情况下,游离型和细胞相关型LPS水平较低,但在头孢他啶存在的情况下则较高。内毒素释放减少似乎是碳青霉烯类抗生素的共同特性。抗生素存在时细菌的形态变化并不能预测其LPS释放效果,因为环丙沙星尽管导致丝状结构形成,但诱导的LPS水平较低。

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