Abstract

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.

Highlights

  • Antibiotics used for treatment of severe bacterial infections have been shown to exert effects on the inflammatory response in addition to their antibacterial effects

  • Antibiotic treatment represents a key component of treatment for IL = interleukin; lipopolysaccharide-binding protein (LBP) = lipopolysacharide-binding protein; MAP = mean arterial pressure; MPAP = mean pulmonary artery pressure; TNF = tumour necrosis factor

  • There is a need to confirm this result in a low-dose endotoxin model, our results indicate that there is no neutralization of endotoxin by tobramycin

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Summary

Introduction

Antibiotics used for treatment of severe bacterial infections have been shown to exert effects on the inflammatory response in addition to their antibacterial effects. Severe bacterial infection [2], but in addition to their antibacterial effect several antibiotics have been shown to exert effects on the inflammatory response. In numerous studies, both in vitro and in vivo, endotoxin in various amounts was released when Gram-negative bacteria were exposed to certain antibiotics, such as β-lactam antibiotics, which are commonly used for the treatment of severe sepsis [1,2,3]. Aminoglycosides have been associated with low release of endotoxin [4,5]

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