Missing effects of zinc in a porcine model of recurrent endotoxemia

<p>Abstract</p> <p>Background</p> <p>Chronic human sepsis often is characterised by the compensatory anti-inflammatory response syndrome (CARS). During CARS, anti-inflammatory cytokines depress the inflammatory response leading to secondary and opportunistic infections....

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Main Authors: Klinge Uwe, Stumpf Michael, Anurov Michael, Klosterhalfen Bernd, Krones Carsten J, Oettinger Alexander P, Schumpelick Volker
Format: Article
Language:English
Published: BMC 2005-10-01
Series:BMC Surgery
Online Access:http://www.biomedcentral.com/1471-2482/5/22
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author Klinge Uwe
Stumpf Michael
Anurov Michael
Klosterhalfen Bernd
Krones Carsten J
Oettinger Alexander P
Schumpelick Volker
author_facet Klinge Uwe
Stumpf Michael
Anurov Michael
Klosterhalfen Bernd
Krones Carsten J
Oettinger Alexander P
Schumpelick Volker
author_sort Klinge Uwe
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Chronic human sepsis often is characterised by the compensatory anti-inflammatory response syndrome (CARS). During CARS, anti-inflammatory cytokines depress the inflammatory response leading to secondary and opportunistic infections. Proved <it>in vitro </it>as well as <it>in vivo</it>, zinc's pro-inflammatory effect might overcome this depression.</p> <p>Methods</p> <p>We used the model of porcine LPS-induced endotoxemia established by Klosterhalfen et al. 10 pigs were divided into two groups (n = 5). Endotoxemia was induced by recurrent intravenous LPS-application (1.0 μg/kg E. coli WO 111:B4) at hours 0, 5, and 12. At hour 10, each group received an intravenous treatment (group I = saline, group II = 5.0 mg/kg elementary zinc). Monitoring included hemodynamics, blood gas analysis, and the thermal dilution technique for the measurement of extravascular lung water and intrapulmonary shunt. Plasma concentrations of IL-6 and TNF-alpha were measured by ELISA. Morphology included weight of the lungs, width of the alveolar septae, and rate of paracentral liver necrosis.</p> <p>Results</p> <p>Zinc's application only trended to partly improve the pulmonary function. Compared to saline, significant differences were very rare. IL-6 and TNF-alpha were predominately measured higher in the zinc group. Again, significance was only reached sporadically. Hemodynamics and morphology revealed no significant differences at all.</p> <p>Conclusion</p> <p>The application of zinc in this model of recurrent endotoxemia is feasible and without harmful effects. However, a protection or restoration of clinical relevance is not evident in our setting. The pulmonary function just trends to improve, cytokine liberation is only partly activated, hemodynamics and morphology were not influenced. Further pre-clinical studies have to define zinc's role as a therapeutic tool during CARS.</p>
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spelling doaj.art-9831696f7ebd4e52b49750edb53865422022-12-22T02:48:21ZengBMCBMC Surgery1471-24822005-10-01512210.1186/1471-2482-5-22Missing effects of zinc in a porcine model of recurrent endotoxemiaKlinge UweStumpf MichaelAnurov MichaelKlosterhalfen BerndKrones Carsten JOettinger Alexander PSchumpelick Volker<p>Abstract</p> <p>Background</p> <p>Chronic human sepsis often is characterised by the compensatory anti-inflammatory response syndrome (CARS). During CARS, anti-inflammatory cytokines depress the inflammatory response leading to secondary and opportunistic infections. Proved <it>in vitro </it>as well as <it>in vivo</it>, zinc's pro-inflammatory effect might overcome this depression.</p> <p>Methods</p> <p>We used the model of porcine LPS-induced endotoxemia established by Klosterhalfen et al. 10 pigs were divided into two groups (n = 5). Endotoxemia was induced by recurrent intravenous LPS-application (1.0 μg/kg E. coli WO 111:B4) at hours 0, 5, and 12. At hour 10, each group received an intravenous treatment (group I = saline, group II = 5.0 mg/kg elementary zinc). Monitoring included hemodynamics, blood gas analysis, and the thermal dilution technique for the measurement of extravascular lung water and intrapulmonary shunt. Plasma concentrations of IL-6 and TNF-alpha were measured by ELISA. Morphology included weight of the lungs, width of the alveolar septae, and rate of paracentral liver necrosis.</p> <p>Results</p> <p>Zinc's application only trended to partly improve the pulmonary function. Compared to saline, significant differences were very rare. IL-6 and TNF-alpha were predominately measured higher in the zinc group. Again, significance was only reached sporadically. Hemodynamics and morphology revealed no significant differences at all.</p> <p>Conclusion</p> <p>The application of zinc in this model of recurrent endotoxemia is feasible and without harmful effects. However, a protection or restoration of clinical relevance is not evident in our setting. The pulmonary function just trends to improve, cytokine liberation is only partly activated, hemodynamics and morphology were not influenced. Further pre-clinical studies have to define zinc's role as a therapeutic tool during CARS.</p>http://www.biomedcentral.com/1471-2482/5/22
spellingShingle Klinge Uwe
Stumpf Michael
Anurov Michael
Klosterhalfen Bernd
Krones Carsten J
Oettinger Alexander P
Schumpelick Volker
Missing effects of zinc in a porcine model of recurrent endotoxemia
BMC Surgery
title Missing effects of zinc in a porcine model of recurrent endotoxemia
title_full Missing effects of zinc in a porcine model of recurrent endotoxemia
title_fullStr Missing effects of zinc in a porcine model of recurrent endotoxemia
title_full_unstemmed Missing effects of zinc in a porcine model of recurrent endotoxemia
title_short Missing effects of zinc in a porcine model of recurrent endotoxemia
title_sort missing effects of zinc in a porcine model of recurrent endotoxemia
url http://www.biomedcentral.com/1471-2482/5/22
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AT stumpfmichael missingeffectsofzincinaporcinemodelofrecurrentendotoxemia
AT anurovmichael missingeffectsofzincinaporcinemodelofrecurrentendotoxemia
AT klosterhalfenbernd missingeffectsofzincinaporcinemodelofrecurrentendotoxemia
AT kronescarstenj missingeffectsofzincinaporcinemodelofrecurrentendotoxemia
AT oettingeralexanderp missingeffectsofzincinaporcinemodelofrecurrentendotoxemia
AT schumpelickvolker missingeffectsofzincinaporcinemodelofrecurrentendotoxemia