抗生素治疗中添加不同臭氧剂量对脓毒症模型细胞因子水平的影响

H. Tüfekçi̇, B. Güven, Enis Bi̇çerer, K. Dere, S. Özkan, G. Daglı
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引用次数: 0

摘要

在大肠杆菌内毒素形成的脓毒症实验模型中,我们旨在研究在抗生素治疗的基础上加入臭氧治疗对促炎和抗炎细胞因子水平的影响。将大鼠分为6组,每组10只。5组大鼠腹腔注射大肠杆菌内毒素形成脓毒症。前3组在抗生素治疗的基础上分别添加0.6 mg/kg、0.9 mg/kg和1.1 mg/kg剂量的臭氧治疗,第4组仅给予抗生素治疗。第5组未治疗。6组与其他各组同时进行血清生理注射。所有治疗均持续5 d。第6天处死大鼠,检测血清IL-1、IL-10、tnf - α水平。IL-1和tnf - α水平明显低于接受臭氧治疗的其他组。在接受臭氧治疗的两组之间的比较中,观察到接受较低剂量的两组的IL-1水平没有显著差异,而tnf - α水平明显低于接受较高剂量的两组。血清IL-10(一种抗炎细胞因子)水平在两组间无显著差异。由此可见,在败血症的抗生素治疗中加入臭氧可能通过抑制炎症过程而对生存率产生积极影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of Different Ozone Doses Added to the Antibiotic Treatment on Cytokine Levels in Experimental Sepsis Model
We aimed to examine the changes caused by ozone therapy added to the antibiotic treatment on proinflammatory and anti-inflammatory cytokine levels in an experimental sepsis model formed with E. coli endotoxin. Rats were divided into 6 groups of 10 rats. Sepsis was formed by dosing 5 groups of rats with intraperitoneal E. coli endotoxin injection. For the first 3 groups, 0.6 mg/kg, 0.9 mg/kg, and 1.1 mg/kg doses of ozone therapy were added to the antibiotic treatment and group-4 only received antibiotic treatment. Group-5 was not treated. Group-6 received intraperitoneal serum physiologic injection simultaneously with the other groups. All treatments were sustained for 5 days. IL-1, IL-10, and TNF-alpha levels were detected in blood serum taken from rats sacrificed on day 6. It was seen that IL-1, TNF-alpha levels are significantly lower than the levels in other groups that received ozone therapy. In the comparisons amongst the groups receiving ozone therapy, it was observed that IL-1 levels do not have a significant difference and TNF-alpha levels are significantly lower in the two groups receiving lower doses than the group receiving a higher dose. There were no significant differences detected between groups at serum levels of IL-10 which is an anti-inflammatory cytokine. It was concluded that ozone added to the antibiotic treatment in sepsis could have a positive effect on survival rates by suppressing inflammatory process.
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