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Role of Nitric Oxide in Depressed Lymphoproliferative Responses and Altered Cytokine Production Following Thermal Injury in Rats

Immunodeficiency follows extensive burns. We investigated some underlying mechanisms in rats, 10 days after a full-thickness skin burn affecting 20% of total body surface area. In both normal and burned rats the splenocyte proliferative response to Con A was linearly and negatively correlated with n...

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Published in:Cellular immunology 1998-06, Vol.186 (2), p.121-132
Main Authors: Masson, Isabelle, Mathieu, Jacques, Nolland, Xavier-Bernard, De Sousa, Martine, Chanaud, Brigitte, Strzalko, Suzanne, Chancerelle, Yves, Kergonou, Jean-François, Giroud, Jean-Paul, Florentin, Irene
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container_title Cellular immunology
container_volume 186
creator Masson, Isabelle
Mathieu, Jacques
Nolland, Xavier-Bernard
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Chanaud, Brigitte
Strzalko, Suzanne
Chancerelle, Yves
Kergonou, Jean-François
Giroud, Jean-Paul
Florentin, Irene
description Immunodeficiency follows extensive burns. We investigated some underlying mechanisms in rats, 10 days after a full-thickness skin burn affecting 20% of total body surface area. In both normal and burned rats the splenocyte proliferative response to Con A was linearly and negatively correlated with nitric oxide (NO) production. In all burned rats, the proliferative response was depressed by more than 80% and NO production corresponded to a nitrite concentration above 20 μM. Proliferative responses in burned rats were fully restored in the presence of 250 μMNG-monomethyl-l-arginine (NMMA). A time course study of NO production in response to Con A, LPS, anti-CD3, and IFN-γ showed that splenic macrophages from burned rats responded to direct and indirect stimuli more rapidly and more intensively than normal macrophages. In the second part of this work, the effect of the overproduction of NO on the synthesis of immunoregulatory and proinflammatory cytokines was investigated. Although it was inhibited, IFN-γ production by splenocytes from burned rats remained sufficient for NO synthase induction and was restored by NMMA. Concomitantly, IL-2 concentration was enhanced but returned to normal in the presence of NMMA. TNF production was halved after burn injury and NMMA partially restored it. In contrast, IL-6 production was enhanced and increased further in the presence of NMMA. Therefore, cytokines were differently affected by burn injury and variously regulated by NO.
doi_str_mv 10.1006/cimm.1998.1296
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ispartof Cellular immunology, 1998-06, Vol.186 (2), p.121-132
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subjects Animals
Burns - immunology
Cell Division
Cells, Cultured
Concanavalin A - pharmacology
Cytokines - biosynthesis
Dexamethasone - pharmacology
Dinoprostone - biosynthesis
Glucocorticoids - pharmacology
Immune Tolerance - immunology
Interferon-gamma - biosynthesis
Interferon-gamma - pharmacology
Interleukin-2 - biosynthesis
Interleukin-6 - biosynthesis
Lipopolysaccharides - pharmacology
Macrophages - immunology
Male
Nitric Oxide - metabolism
Nitric Oxide - physiology
Rats
Rats, Wistar
Spleen - cytology
Time Factors
Tumor Necrosis Factor-alpha - biosynthesis
title Role of Nitric Oxide in Depressed Lymphoproliferative Responses and Altered Cytokine Production Following Thermal Injury in Rats
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