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Aging and sarcopenia associate with specific interactions between gut microbes, serum biomarkers and host physiology in rats
The microbiome has been demonstrated to play an integral role in the maintenance of many aspects of health that are also associated with aging. In order to identify areas of potential exploration and intervention, we simultaneously characterized age-related alterations in gut microbiome, muscle phys...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559170/ https://www.ncbi.nlm.nih.gov/pubmed/28783713 http://dx.doi.org/10.18632/aging.101262 |
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author | Siddharth, Jay Chakrabarti, Anirikh Pannérec, Alice Karaz, Sonia Morin-Rivron, Delphine Masoodi, Mojgan Feige, Jerome N. Parkinson, Scott James |
author_facet | Siddharth, Jay Chakrabarti, Anirikh Pannérec, Alice Karaz, Sonia Morin-Rivron, Delphine Masoodi, Mojgan Feige, Jerome N. Parkinson, Scott James |
author_sort | Siddharth, Jay |
collection | PubMed |
description | The microbiome has been demonstrated to play an integral role in the maintenance of many aspects of health that are also associated with aging. In order to identify areas of potential exploration and intervention, we simultaneously characterized age-related alterations in gut microbiome, muscle physiology and serum proteomic and lipidomic profiles in aged rats to define an integrated signature of the aging phenotype. We demonstrate that aging skews the composition of the gut microbiome, in particular by altering the Sutterella to Barneseilla ratio, and alters the metabolic potential of intestinal bacteria. Age-related changes of the gut microbiome were associated with the physiological decline of musculoskeletal function, and with molecular markers of nutrient processing/availability, and inflammatory/immune status in aged versus adult rats. Altogether, our study highlights that aging leads to a complex interplay between the microbiome and host physiology, and provides candidate microbial species to target physical and metabolic decline during aging by modulating gut microbial ecology. |
format | Online Article Text |
id | pubmed-5559170 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-55591702017-09-26 Aging and sarcopenia associate with specific interactions between gut microbes, serum biomarkers and host physiology in rats Siddharth, Jay Chakrabarti, Anirikh Pannérec, Alice Karaz, Sonia Morin-Rivron, Delphine Masoodi, Mojgan Feige, Jerome N. Parkinson, Scott James Aging (Albany NY) Research Paper The microbiome has been demonstrated to play an integral role in the maintenance of many aspects of health that are also associated with aging. In order to identify areas of potential exploration and intervention, we simultaneously characterized age-related alterations in gut microbiome, muscle physiology and serum proteomic and lipidomic profiles in aged rats to define an integrated signature of the aging phenotype. We demonstrate that aging skews the composition of the gut microbiome, in particular by altering the Sutterella to Barneseilla ratio, and alters the metabolic potential of intestinal bacteria. Age-related changes of the gut microbiome were associated with the physiological decline of musculoskeletal function, and with molecular markers of nutrient processing/availability, and inflammatory/immune status in aged versus adult rats. Altogether, our study highlights that aging leads to a complex interplay between the microbiome and host physiology, and provides candidate microbial species to target physical and metabolic decline during aging by modulating gut microbial ecology. Impact Journals LLC 2017-07-17 /pmc/articles/PMC5559170/ /pubmed/28783713 http://dx.doi.org/10.18632/aging.101262 Text en Copyright: © 2017 Siddharth et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Paper Siddharth, Jay Chakrabarti, Anirikh Pannérec, Alice Karaz, Sonia Morin-Rivron, Delphine Masoodi, Mojgan Feige, Jerome N. Parkinson, Scott James Aging and sarcopenia associate with specific interactions between gut microbes, serum biomarkers and host physiology in rats |
title | Aging and sarcopenia associate with specific interactions between gut microbes, serum biomarkers and host physiology in rats |
title_full | Aging and sarcopenia associate with specific interactions between gut microbes, serum biomarkers and host physiology in rats |
title_fullStr | Aging and sarcopenia associate with specific interactions between gut microbes, serum biomarkers and host physiology in rats |
title_full_unstemmed | Aging and sarcopenia associate with specific interactions between gut microbes, serum biomarkers and host physiology in rats |
title_short | Aging and sarcopenia associate with specific interactions between gut microbes, serum biomarkers and host physiology in rats |
title_sort | aging and sarcopenia associate with specific interactions between gut microbes, serum biomarkers and host physiology in rats |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559170/ https://www.ncbi.nlm.nih.gov/pubmed/28783713 http://dx.doi.org/10.18632/aging.101262 |
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