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The sex-specific metabolic signature of C57BL/6NRj mice during aging
Due to intact reactive oxygen species homeostasis and glucose metabolism, C57BL/6NRj mice are especially suitable to study cellular alterations in metabolism. We applied Nuclear Magnetic resonance spectroscopy to analyze five different tissues of this mouse strain during aging and included female an...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9726821/ https://www.ncbi.nlm.nih.gov/pubmed/36473898 http://dx.doi.org/10.1038/s41598-022-25396-8 |
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author | Bresilla, Doruntina Habisch, Hansjoerg Pritišanac, Iva Zarse, Kim Parichatikanond, Warisara Ristow, Michael Madl, Tobias Madreiter-Sokolowski, Corina T. |
author_facet | Bresilla, Doruntina Habisch, Hansjoerg Pritišanac, Iva Zarse, Kim Parichatikanond, Warisara Ristow, Michael Madl, Tobias Madreiter-Sokolowski, Corina T. |
author_sort | Bresilla, Doruntina |
collection | PubMed |
description | Due to intact reactive oxygen species homeostasis and glucose metabolism, C57BL/6NRj mice are especially suitable to study cellular alterations in metabolism. We applied Nuclear Magnetic resonance spectroscopy to analyze five different tissues of this mouse strain during aging and included female and male mice aged 3, 6, 12, and 24 months. Metabolite signatures allowed separation between the age groups in all tissues, and we identified the most prominently changing metabolites in female and male tissues. A refined analysis of individual metabolite levels during aging revealed an early onset of age-related changes at 6 months, sex-specific differences in the liver, and a biphasic pattern for various metabolites in the brain, heart, liver, and lung. In contrast, a linear decrease of amino acids was apparent in muscle tissues. Based on these results, we assume that age-related metabolic alterations happen at a comparably early aging state and are potentially associated with a metabolic switch. Moreover, identified differences between female and male tissues stress the importance of distinguishing between sexes when studying age-related changes and developing new treatment approaches. Besides, metabolomic features seem to be highly dependent on the genetic background of mouse strains. |
format | Online Article Text |
id | pubmed-9726821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97268212022-12-08 The sex-specific metabolic signature of C57BL/6NRj mice during aging Bresilla, Doruntina Habisch, Hansjoerg Pritišanac, Iva Zarse, Kim Parichatikanond, Warisara Ristow, Michael Madl, Tobias Madreiter-Sokolowski, Corina T. Sci Rep Article Due to intact reactive oxygen species homeostasis and glucose metabolism, C57BL/6NRj mice are especially suitable to study cellular alterations in metabolism. We applied Nuclear Magnetic resonance spectroscopy to analyze five different tissues of this mouse strain during aging and included female and male mice aged 3, 6, 12, and 24 months. Metabolite signatures allowed separation between the age groups in all tissues, and we identified the most prominently changing metabolites in female and male tissues. A refined analysis of individual metabolite levels during aging revealed an early onset of age-related changes at 6 months, sex-specific differences in the liver, and a biphasic pattern for various metabolites in the brain, heart, liver, and lung. In contrast, a linear decrease of amino acids was apparent in muscle tissues. Based on these results, we assume that age-related metabolic alterations happen at a comparably early aging state and are potentially associated with a metabolic switch. Moreover, identified differences between female and male tissues stress the importance of distinguishing between sexes when studying age-related changes and developing new treatment approaches. Besides, metabolomic features seem to be highly dependent on the genetic background of mouse strains. Nature Publishing Group UK 2022-12-06 /pmc/articles/PMC9726821/ /pubmed/36473898 http://dx.doi.org/10.1038/s41598-022-25396-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Bresilla, Doruntina Habisch, Hansjoerg Pritišanac, Iva Zarse, Kim Parichatikanond, Warisara Ristow, Michael Madl, Tobias Madreiter-Sokolowski, Corina T. The sex-specific metabolic signature of C57BL/6NRj mice during aging |
title | The sex-specific metabolic signature of C57BL/6NRj mice during aging |
title_full | The sex-specific metabolic signature of C57BL/6NRj mice during aging |
title_fullStr | The sex-specific metabolic signature of C57BL/6NRj mice during aging |
title_full_unstemmed | The sex-specific metabolic signature of C57BL/6NRj mice during aging |
title_short | The sex-specific metabolic signature of C57BL/6NRj mice during aging |
title_sort | sex-specific metabolic signature of c57bl/6nrj mice during aging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9726821/ https://www.ncbi.nlm.nih.gov/pubmed/36473898 http://dx.doi.org/10.1038/s41598-022-25396-8 |
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