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Determinants of gene expression in the human liver: Impact of aging and sex on xenobiotic metabolism.
Corton, J Christopher; Lee, Janice S; Liu, Jie; Ren, Hongzu; Vallanat, Beena; DeVito, Michael.
Afiliación
  • Corton JC; Center for Computational Toxicology and Exposure, US EPA, Research Triangle Park, NC 27711, United States of America. Electronic address: corton.chris@epa.gov.
  • Lee JS; Center for Public Health and Environmental Assessment, US EPA, Research Triangle Park, NC 27711, United States of America. Electronic address: lee.janices@epa.gov.
  • Liu J; Center for Computational Toxicology and Exposure, US EPA, Research Triangle Park, NC 27711, United States of America. Electronic address: Liu.jie@epa.gov.
  • Ren H; Center for Public Health and Environmental Assessment, US EPA, Research Triangle Park, NC 27711, United States of America. Electronic address: ren.hongzu@epa.gov.
  • Vallanat B; Center for Computational Toxicology and Exposure, US EPA, Research Triangle Park, NC 27711, United States of America. Electronic address: vallanat.beena@epa.gov.
  • DeVito M; Center for Computational Toxicology and Exposure, US EPA, Research Triangle Park, NC 27711, United States of America. Electronic address: devito.michael@epa.gov.
Exp Gerontol ; 169: 111976, 2022 11.
Article en En | MEDLINE | ID: mdl-36244585
ABSTRACT
There is a need to characterize the potential susceptibility of older adults to toxicity from environmental chemical exposures. Liver xenobiotic metabolizing enzymes (XMEs) play important roles in detoxifying and eliminating xenobiotics. We examined global gene expression in the livers of young (21-45 years) and old (69+ years) men and women. Differentially expressed genes (DEG) were identified using two-way ANOVA (p ≤ 0.05). We identified 1437 and 1670 DEGs between young and old groups in men and women, respectively. Only a minor number of the total number of genes overlapped (146 genes). Aging increased or decreased pathways involved in inflammation and intermediary metabolism, respectively. Aging led to numerous changes in the expression of XME genes or genes known to control their expression (~90 genes). Out of 10 cytochrome P450s activities examined, there were increased activities of CYP1A2 and CYP2C9 enzymes in the old groups. We also identified sex-dependent genes that were more numerous in the young group (1065) than in the old group (202) and included changes in XMEs. These studies indicate that the livers from aging humans when compared to younger adults exhibit changes in XMEs that may lead to differences in the metabolism of xenobiotics.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Xenobióticos / Sistema Enzimático del Citocromo P-450 Límite: Aged / Female / Humans / Male Idioma: En Revista: Exp Gerontol Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Xenobióticos / Sistema Enzimático del Citocromo P-450 Límite: Aged / Female / Humans / Male Idioma: En Revista: Exp Gerontol Año: 2022 Tipo del documento: Article
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