Halbach Jonathan L, Wang Andrew W, Hawisher Dennis, Cauvi David M, Lizardo Radhames E, Rosas Joseph, Reyes Tony, Escobedo Omar, Bickler Stephen W, Coimbra Raul, De Maio Antonio
Department of Surgery, Naval Medical Center San Diego, San Diego, California, USA.
Division of Trauma, Critical Care, Burns and Acute Injury, Department of Surgery, School of Medicine, University of California, La Jolla, California, USA.
Infect Immun. 2017 Nov 17;85(12). doi: 10.1128/IAI.00664-17. Print 2017 Dec.
Sepsis remains a major health problem at the levels of mortality, morbidity, and economic burden to the health care system, a condition that is aggravated by the development of secondary conditions such as septic shock and multiple-organ failure. Our current understanding of the etiology of human sepsis has advanced, at least in part, due to the use of experimental animal models, particularly the model of cecum ligation and puncture (CLP). Antibiotic treatment has been commonly used in this model to closely mirror the treatment of human septic patients. However, whether their use may obscure the elucidation of the cellular and molecular mechanisms involved in the septic response is questionable. The objective of the present study was to determine the effect of antibiotic treatment in the outcome of a fulminant model of CLP. Various dosing strategies were used for the administration of imipenem, which has broad-spectrum coverage of enteric bacteria. No statistically significant differences in the survival of mice were observed between the different antibiotic dosing strategies and no treatment, suggesting that live bacteria may not be the only factor inducing septic shock. To further investigate this hypothesis, mice were challenged with sterilized or unsterilized cecal contents. We found that exposure of mice to sterilized cecal contents also resulted in a high mortality rate. Therefore, it is possible that bacterial debris, apart from bacterial proliferation, triggers a septic response and contributes to mortality in this model, suggesting that additional factors are involved in the development of septic shock.
脓毒症在死亡率、发病率以及对医疗保健系统造成的经济负担方面仍然是一个重大的健康问题,而诸如感染性休克和多器官功能衰竭等继发性病症的出现则加剧了这种情况。我们目前对人类脓毒症病因的理解至少在一定程度上得益于实验动物模型的使用,尤其是盲肠结扎和穿刺(CLP)模型。在这个模型中,抗生素治疗被普遍用于紧密模拟人类脓毒症患者的治疗。然而,抗生素的使用是否会模糊对脓毒症反应所涉及的细胞和分子机制的阐释,这是值得怀疑的。本研究的目的是确定抗生素治疗对CLP暴发性模型结果的影响。使用了各种给药策略来给予亚胺培南,它对肠道细菌具有广谱覆盖。在不同抗生素给药策略组与未治疗组之间,未观察到小鼠存活率存在统计学上的显著差异,这表明活菌可能不是诱导感染性休克的唯一因素。为了进一步研究这一假设,用灭菌或未灭菌的盲肠内容物对小鼠进行攻击。我们发现,让小鼠接触灭菌的盲肠内容物也导致了高死亡率。因此,除了细菌增殖外,细菌碎片可能触发脓毒症反应并导致该模型中的死亡率,这表明感染性休克的发生还涉及其他因素。