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Interleukin 10 reduces the release of tumor necrosis factor and prevents lethality in experimental endotoxemia

Because of its ability to efficiently inhibit in vitro cytokine production by activated macrophages, we hypothesized that interleukin (IL) 10 might be of particular interest in preventing endotoxin-induced toxicity. We therefore examined the effects of IL-10 administration before lipopolysaccharide...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1993
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190913/
https://www.ncbi.nlm.nih.gov/pubmed/8426124
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description Because of its ability to efficiently inhibit in vitro cytokine production by activated macrophages, we hypothesized that interleukin (IL) 10 might be of particular interest in preventing endotoxin-induced toxicity. We therefore examined the effects of IL-10 administration before lipopolysaccharide (LPS) challenge in mice. A marked reduction in the amounts of LPS-induced tumor necrosis factor (TNF) release in the circulation was observed after IL-10 pretreatment at doses at low as 10 U. IL-10 also efficiently prevented the hypothermia generated by the injection of 100 micrograms LPS. Finally, pretreatment with a single injection of 1,000 U IL-10 completely prevented the mortality consecutive to the challenge with 500 micrograms LPS, a dose that was lethal in 50% of the control mice. We conclude that IL-10 inhibits in vivo TNF secretion and protects against the lethality of endotoxin in a murine model of septic shock.
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spelling pubmed-21909132008-04-16 Interleukin 10 reduces the release of tumor necrosis factor and prevents lethality in experimental endotoxemia J Exp Med Articles Because of its ability to efficiently inhibit in vitro cytokine production by activated macrophages, we hypothesized that interleukin (IL) 10 might be of particular interest in preventing endotoxin-induced toxicity. We therefore examined the effects of IL-10 administration before lipopolysaccharide (LPS) challenge in mice. A marked reduction in the amounts of LPS-induced tumor necrosis factor (TNF) release in the circulation was observed after IL-10 pretreatment at doses at low as 10 U. IL-10 also efficiently prevented the hypothermia generated by the injection of 100 micrograms LPS. Finally, pretreatment with a single injection of 1,000 U IL-10 completely prevented the mortality consecutive to the challenge with 500 micrograms LPS, a dose that was lethal in 50% of the control mice. We conclude that IL-10 inhibits in vivo TNF secretion and protects against the lethality of endotoxin in a murine model of septic shock. The Rockefeller University Press 1993-02-01 /pmc/articles/PMC2190913/ /pubmed/8426124 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Interleukin 10 reduces the release of tumor necrosis factor and prevents lethality in experimental endotoxemia
title Interleukin 10 reduces the release of tumor necrosis factor and prevents lethality in experimental endotoxemia
title_full Interleukin 10 reduces the release of tumor necrosis factor and prevents lethality in experimental endotoxemia
title_fullStr Interleukin 10 reduces the release of tumor necrosis factor and prevents lethality in experimental endotoxemia
title_full_unstemmed Interleukin 10 reduces the release of tumor necrosis factor and prevents lethality in experimental endotoxemia
title_short Interleukin 10 reduces the release of tumor necrosis factor and prevents lethality in experimental endotoxemia
title_sort interleukin 10 reduces the release of tumor necrosis factor and prevents lethality in experimental endotoxemia
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190913/
https://www.ncbi.nlm.nih.gov/pubmed/8426124