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

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.

[1]  A. Artenstein,et al.  Inhibition of endotoxin reactivity by aminoglycosides. , 1989, The Journal of antimicrobial chemotherapy.

[2]  G. Deby-dupont,et al.  Oxidant-scavenging activities of beta-lactam agents , 2005, European Journal of Clinical Microbiology and Infectious Diseases.

[3]  M. Evans,et al.  Effect of antibiotic class and concentration on the release of lipopolysaccharide from Escherichia coli. , 1993, The Journal of infectious diseases.

[4]  D. Traber,et al.  CARDIOPULMONARY AND SPLANCHNIC BLOOD FLOW DURING 48 HOURS OF A CONTINUOUS INFUSION OF ENDOTOXIN IN CONSCIOUS PIGS: A MODEL OF HYPERDYNAMIC SHOCK , 2000, Shock.

[5]  F. Dallegri,et al.  Cytoprotection against neutrophil-delivered oxidant attack by antibiotics. , 1991, Biochemical pharmacology.

[6]  J. Vincent,et al.  Yearbook of Intensive Care and Emergency Medicine , 1995, Yearbook of Intensive Care and Emergency Medicine.

[7]  A. Cantin,et al.  Protection by antibiotics against myeloperoxidase-dependent cytotoxicity to lung epithelial cells in vitro. , 1993, The Journal of clinical investigation.

[8]  J. Shenep,et al.  Role of antibiotic class in the rate of liberation of endotoxin during therapy for experimental gram-negative bacterial sepsis. , 1985, The Journal of infectious diseases.

[9]  G. Deby-dupont,et al.  Neutrophil-induced Oxidative Stress , 1996 .

[10]  K. Rieger,et al.  Effect of increased cardiac output on liver blood flow, oxygen exchange and metabolic rate during longterm endotoxin‐induced shock in pigs , 1998, British journal of pharmacology.

[11]  I. Odenholt,et al.  Variation in the Propensity to Release Endotoxin after Cefuroxime Exposure in Different Gram-negative Bacteria: Uniform and Dose-dependent Reduction by the Addition of Tobramycin , 2003, Scandinavian journal of infectious diseases.

[12]  S. Deventer,et al.  Clinical relevance of antibiotic-induced endotoxin release , 1994, Antimicrobial Agents and Chemotherapy.

[13]  R. Berzofsky,et al.  Chromogenic Limulus amoebocyte lysate assay for rapid detection of gram-negative bacteriuria , 1985, Journal of clinical microbiology.

[14]  M. Lamy,et al.  Oxygen consumption and electron spin resonance studies of free radical production by alveolar cells exposed to anoxia: inhibiting effects of the antibiotic ceftazidime , 2002, Redox report : communications in free radical research.

[15]  L. Lind,et al.  Hypocalcemia during porcine endotoxemic shock: Effects of calcium administration , 2000, Critical care medicine.

[16]  J. Hurley,et al.  Antibiotic-induced release of endotoxin: a reappraisal. , 1992, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[17]  L. Lind,et al.  Microdialysis-evaluated myocardial cyclooxygenase-mediated inflammation and early circulatory depression in porcine endotoxemia. , 2003, Critical care medicine.

[18]  M. Lamy,et al.  The antibiotic ceftazidime is a singlet oxygen quencher as demonstrated by ultra-weak chemiluminescence and by inhibition of AAP consumption. , 1998, Biochimica et biophysica acta.

[19]  J. Bring,et al.  Endotoxin release from Escherichia coli after exposure to tobramycin: dose-dependency and reduction in cefuroxime-induced endotoxin release. , 2000, Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases.

[20]  M. Suematsu,et al.  ERK and p38 MAPK, but not NF-&kgr;B, Are Critically Involved in Reactive Oxygen Species–Mediated Induction of IL-6 by Angiotensin II in Cardiac Fibroblasts , 2001, Circulation research.

[21]  C. Matthias,et al.  Influence of ozone and nitrogen dioxide on histamine and interleukin formation in a human nasal mucosa culture system. , 1999, American journal of respiratory cell and molecular biology.

[22]  J. Nielsen,et al.  An experimental randomized study of five different ventilatory modes in a piglet model of severe respiratory distress , 2005, Intensive Care Medicine.