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Sex differences in inflammatory cytokine production in hepatic ischemia-reperfusion

BACKGROUND: The inflammatory response to hepatic ischemia-reperfusion (I/R) is associated with an increase in cytokine production. Studies have documented that sex hormones modulate both the innate and adaptive immune responses, and that females are more robust than males. The aim of this study was...

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Autores principales: Crockett, Elahé T, Spielman, William, Dowlatshahi, Shadi, He, Jun
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1764413/
https://www.ncbi.nlm.nih.gov/pubmed/17177998
http://dx.doi.org/10.1186/1476-9255-3-16
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author Crockett, Elahé T
Spielman, William
Dowlatshahi, Shadi
He, Jun
author_facet Crockett, Elahé T
Spielman, William
Dowlatshahi, Shadi
He, Jun
author_sort Crockett, Elahé T
collection PubMed
description BACKGROUND: The inflammatory response to hepatic ischemia-reperfusion (I/R) is associated with an increase in cytokine production. Studies have documented that sex hormones modulate both the innate and adaptive immune responses, and that females are more robust than males. The aim of this study was to determine whether a sex difference in cytokine response to hepatic I/R exists under normal pathophysiologic condition without hormone intervention. METHODS: Adult C57BL/6 mice underwent 90 min of hepatic ischemia followed by various reperfusion periods (0, 1.5, 3, 6 hr). Plasma cytokine TNF-α, IL-6, MIP-2, and KC were measured. Liver injury was assessed by plasma alanine transaminase (ALT) levels and liver histopathology. RESULTS: A reperfusion time-dependent increase in hepatocellular injury was observed in both males and females, as indicated by increasing levels of plasma ALT and liver histopathology. The plasma cytokines were significantly increased in both female and male I/R groups compared to their respective sham counterparts. However, there was a significant difference in cytokine kinetics between the female and male I/R groups. Female mice initially had a higher level of IL-6, KC, and MIP-2 in response to I/R, which began to decline after 3 hr of reperfusion and were significantly lower than the male I/R counterparts by 6 hr of reperfusion. In contrast, the hepatocellular injury and TNF production were only moderately lower in female IR than male IR. CONCLUSION: The study underscores role of the gender in differential inflammatory cytokine expression in response to hepatic I/R, which may reflect the host response outcome.
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spelling pubmed-17644132007-01-06 Sex differences in inflammatory cytokine production in hepatic ischemia-reperfusion Crockett, Elahé T Spielman, William Dowlatshahi, Shadi He, Jun J Inflamm (Lond) Research BACKGROUND: The inflammatory response to hepatic ischemia-reperfusion (I/R) is associated with an increase in cytokine production. Studies have documented that sex hormones modulate both the innate and adaptive immune responses, and that females are more robust than males. The aim of this study was to determine whether a sex difference in cytokine response to hepatic I/R exists under normal pathophysiologic condition without hormone intervention. METHODS: Adult C57BL/6 mice underwent 90 min of hepatic ischemia followed by various reperfusion periods (0, 1.5, 3, 6 hr). Plasma cytokine TNF-α, IL-6, MIP-2, and KC were measured. Liver injury was assessed by plasma alanine transaminase (ALT) levels and liver histopathology. RESULTS: A reperfusion time-dependent increase in hepatocellular injury was observed in both males and females, as indicated by increasing levels of plasma ALT and liver histopathology. The plasma cytokines were significantly increased in both female and male I/R groups compared to their respective sham counterparts. However, there was a significant difference in cytokine kinetics between the female and male I/R groups. Female mice initially had a higher level of IL-6, KC, and MIP-2 in response to I/R, which began to decline after 3 hr of reperfusion and were significantly lower than the male I/R counterparts by 6 hr of reperfusion. In contrast, the hepatocellular injury and TNF production were only moderately lower in female IR than male IR. CONCLUSION: The study underscores role of the gender in differential inflammatory cytokine expression in response to hepatic I/R, which may reflect the host response outcome. BioMed Central 2006-12-19 /pmc/articles/PMC1764413/ /pubmed/17177998 http://dx.doi.org/10.1186/1476-9255-3-16 Text en Copyright © 2006 Crockett et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Crockett, Elahé T
Spielman, William
Dowlatshahi, Shadi
He, Jun
Sex differences in inflammatory cytokine production in hepatic ischemia-reperfusion
title Sex differences in inflammatory cytokine production in hepatic ischemia-reperfusion
title_full Sex differences in inflammatory cytokine production in hepatic ischemia-reperfusion
title_fullStr Sex differences in inflammatory cytokine production in hepatic ischemia-reperfusion
title_full_unstemmed Sex differences in inflammatory cytokine production in hepatic ischemia-reperfusion
title_short Sex differences in inflammatory cytokine production in hepatic ischemia-reperfusion
title_sort sex differences in inflammatory cytokine production in hepatic ischemia-reperfusion
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1764413/
https://www.ncbi.nlm.nih.gov/pubmed/17177998
http://dx.doi.org/10.1186/1476-9255-3-16
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