Differences in the hepatic signal transcription pathway and cytokine expression between thermal injury and sepsis

Klein, Dagmar and Einspanier, Ralf and Bolder, Ulrich and Jeschke, Marc G. (2003) Differences in the hepatic signal transcription pathway and cytokine expression between thermal injury and sepsis. SHOCK, 20 (6). pp. 536-543. ISSN 1073-2322

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Abstract

Inflammation and catabolism in response to trauma, surgery, critical illness or bacteria lead to a compromise of essential organs, which can lead to prolonged clinical stay and even death. Mediators responsible for catabolism were thought to be proinflammatory cytokines, but recently the focus has shifted to signal transduction. The purpose of the present study was to determine differences between two pathophysiologic states, sepsis and thermal injury, in signal transduction and cytokine expression and thus define the importance of the signal transcription pathway. Rats were randomly divided to either receive lipopolysaccharide (3 mg/kg body weight or a 30% total body surface area burn) or they received no treatment and served as controls. Animals were sacrificed 1, 2, 5, and 7 days postinsult and serum and liver harvested for analysis. A thermal injury appeared to have a slow release and expression of signal transcription factors and cytokines and a sepsis showed a rapid increase of mediators and also a fast decrease. The changes in cytokine profiles after burn, particularly interleukin-10 and macrophage inhibitory factor, appear to be mediated by C/EBP-beta and STAT-3, whereas after the induction of a sepsis, tumor necrosis factor and interleukin-6 are mainly mediated by STAT-5. Based on our findings we suggest that the pathophysiologic state of a thermal injury is not comparable with sepsis in association with signal transcription factors and the differences in intracellular and extracellular signaling therefore opens new ideas for therapeutic options.

Item Type: Article
Uncontrolled Keywords: ACUTE-PHASE RESPONSE; GROWTH-FACTOR-I; SEPTIC SHOCK; GENE-TRANSCRIPTION; IMPROVES SURVIVAL; CRITICAL ILLNESS; HORMONE; INTERLEUKIN-1; SUPPRESSORS; CACHECTIN; sepsis; inflammation; trauma; burn; insulin; immunity; liver; signaling
Subjects: 600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Lehrstuhl für Chirurgie
Depositing User: Dr. Gernot Deinzer
Date Deposited: 25 Aug 2021 09:53
Last Modified: 25 Aug 2021 09:53
URI: https://pred.uni-regensburg.de/id/eprint/38386

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