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Endotoxin neutralization and anti-inflammatory effects of tobramycin and ceftazidime in porcine endotoxin shock

机译:内毒素中和妥布霉素和头孢他啶对猪内毒素休克的抗炎作用

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IntroductionAntibiotics used for treatment of severe bacterial infections have been shown to exert effects on the inflammatory response in addition to their antibacterial effects. The aim of the present study was to investigate whether the biological effects of endotoxin in a porcine model could be neutralized by tobramycin, and whether tobramycin or ceftazidime was able to modulate the inflammatory response.MethodThirteen piglets were subjected to endotoxin infusion at an initial rate of 4 μg/kg per hour, which was reduced to 1 μg/kg per hour after 30 min. Before endotoxin infusion, the animals received saline (n = 4), ceftazidime (n = 5), or tobramycin (n = 4) at clinically relevant doses. Physiological parameters were measured and blood samples were taken hourly for 6 hours for analysis of tumour necrosis factor-α, IL-6 and endotoxin concentrations.ResultsAll of the animals exhibited physiological signs of severe sepsis without major differences between the groups. Plasma endotoxin concentration was stable after 1 hour. There were no differences in endotoxin concentration or initial tumour necrosis factor-α and IL-6 concentrations between the groups. At 6 hours the IL-6 concentration was significantly lower in the ceftazidime group than in the saline group (P < 0.05), and in both the ceftazidime and the tobramycin groups there were significantly greater reductions from peak values (P < 0.05).ConclusionThere was no neutralization of the biological effects of endotoxin in this porcine model. However, our data indicate a possible anti-inflammatory effect exerted by both ceftazidime and tobramycin, which manifested as a significantly greater reduction in IL-6 in comparison with the untreated group.
机译:引言已证明,用于治疗严重细菌感染的抗生素除具有抗菌作用外,还对炎症反应产生作用。本研究的目的是研究猪模型中内毒素的生物学效应是否可以被妥布霉素中和,以及妥布霉素或头孢他啶是否能够调节炎症反应。方法对13头仔猪以初始速率进行内毒素输注每小时4μg/ kg,在30分钟后降至每小时1μg/ kg。在输注内毒素之前,动物接受临床相关剂量的生理盐水(n = 4),头孢他啶(n = 5)或妥布霉素(n = 4)。测量生理参数,每小时采集血样6小时,分析肿瘤坏死因子-α,IL-6和内毒素浓度。结果所有动物均表现出严重脓毒症的生理征象,两组之间无重大差异。 1小时后血浆内毒素浓度稳定。两组之间内毒素浓度或初始肿瘤坏死因子-α和IL-6浓度无差异。在6小时时,头孢他啶组的IL-6浓度显着低于生理盐水组(P <0.05),并且头孢他啶组和妥布霉素组的IL-6浓度均从峰值显着降低(P <0.05)。在该猪模型中没有中和内毒素的生物学作用。然而,我们的数据表明头孢他啶和妥布霉素均可能发挥抗炎作用,与未治疗组相比,IL-6的降低明显更大。

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