Crosby H A, Bion J F, Penn C W, Elliott T S
Department of Clinical Microbiology, Queen Elizabeth Hospital, Birmingham.
J Med Microbiol. 1994 Jan;40(1):23-30. doi: 10.1099/00222615-40-1-23.
The ability of cefotaxime, ciprofloxacin, piperacillin and tobramycin to cause release of endotoxin was examined in vitro with cultures of Enterobacter cloacae and Escherichia coli. Endotoxin was measured by a quantitative limulus amoebocyte lysate assay and its presence was confirmed by silver staining of the lipopolysaccharide moiety following SDS-PAGE. The morphology of the bacteria during antibiotic exposure was examined by scanning electronmicroscopy. Cefotaxime, ciprofloxacin and piperacillin caused significant endotoxin release, correlating with their ability to affect cell-wall morphology, causing filamentation, wall breakage and cell lysis. In contrast, little endotoxin was released when bacteria were exposed to tobramycin and no morphological changes were observed when bacteria were exposed to bactericidal concentrations of this aminoglycoside. Its antimicrobial spectrum and bactericidal activity make tobramycin an appropriate agent for treatment of sepsis caused by gram-negative bacteria and its lack of propensity to elicit excessive release of endotoxin may avoid exacerbation of endotoxin-related shock in sepsis.
利用阴沟肠杆菌和大肠杆菌培养物在体外检测了头孢噻肟、环丙沙星、哌拉西林和妥布霉素导致内毒素释放的能力。通过定量鲎试剂法测定内毒素,并在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)后对脂多糖部分进行银染来确认内毒素的存在。通过扫描电子显微镜检查抗生素作用期间细菌的形态。头孢噻肟、环丙沙星和哌拉西林导致大量内毒素释放,这与其影响细胞壁形态、导致丝状化、细胞壁破裂和细胞裂解的能力相关。相比之下,当细菌暴露于妥布霉素时几乎没有内毒素释放,并且当细菌暴露于该氨基糖苷类的杀菌浓度时未观察到形态变化。妥布霉素的抗菌谱和杀菌活性使其成为治疗革兰氏阴性菌引起的败血症的合适药物,并且其不易引发内毒素过度释放的特性可能避免败血症中内毒素相关休克的加重。