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Metformin alters skeletal muscle transcriptome adaptations to resistance training in older adults
Evidence from clinical trials and observational studies suggests that both progressive resistance exercise training (PRT) and metformin delay a variety of age-related morbidities. Previously, we completed a clinical trial testing the effects of 14 weeks of PRT + metformin (metPRT) compared to PRT wi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7655218/ https://www.ncbi.nlm.nih.gov/pubmed/33071237 http://dx.doi.org/10.18632/aging.104096 |
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author | Kulkarni, Ameya S. Peck, Bailey D. Walton, R. Grace Kern, Philip A. Mar, Jessica C. Windham, Samuel T. Bamman, Marcas M. Barzilai, Nir Peterson, Charlotte A. |
author_facet | Kulkarni, Ameya S. Peck, Bailey D. Walton, R. Grace Kern, Philip A. Mar, Jessica C. Windham, Samuel T. Bamman, Marcas M. Barzilai, Nir Peterson, Charlotte A. |
author_sort | Kulkarni, Ameya S. |
collection | PubMed |
description | Evidence from clinical trials and observational studies suggests that both progressive resistance exercise training (PRT) and metformin delay a variety of age-related morbidities. Previously, we completed a clinical trial testing the effects of 14 weeks of PRT + metformin (metPRT) compared to PRT with placebo (plaPRT) on muscle hypertrophy in older adults. We found that metformin blunted PRT-induced muscle hypertrophic response. To understand potential mechanisms underlying the inhibitory effect of metformin on PRT, we analyzed the muscle transcriptome in 23 metPRT and 24 plaPRT participants. PRT significantly increased expression of genes involved in extracellular matrix remodeling pathways, and downregulated RNA processing pathways in both groups, however, metformin attenuated the number of differentially expressed genes within these pathways compared to plaPRT. Pathway analysis showed that genes unique to metPRT modulated aging-relevant pathways, such as cellular senescence and autophagy. Differentially expressed genes from baseline biopsies in older adults compared to resting muscle from young volunteers were reduced following PRT in plaPRT and were further reduced in metPRT. We suggest that although metformin may blunt pathways induced by PRT to promote muscle hypertrophy, adjunctive metformin during PRT may have beneficial effects on aging-associated pathways in muscle from older adults. |
format | Online Article Text |
id | pubmed-7655218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-76552182020-11-19 Metformin alters skeletal muscle transcriptome adaptations to resistance training in older adults Kulkarni, Ameya S. Peck, Bailey D. Walton, R. Grace Kern, Philip A. Mar, Jessica C. Windham, Samuel T. Bamman, Marcas M. Barzilai, Nir Peterson, Charlotte A. Aging (Albany NY) Priority Research Paper Evidence from clinical trials and observational studies suggests that both progressive resistance exercise training (PRT) and metformin delay a variety of age-related morbidities. Previously, we completed a clinical trial testing the effects of 14 weeks of PRT + metformin (metPRT) compared to PRT with placebo (plaPRT) on muscle hypertrophy in older adults. We found that metformin blunted PRT-induced muscle hypertrophic response. To understand potential mechanisms underlying the inhibitory effect of metformin on PRT, we analyzed the muscle transcriptome in 23 metPRT and 24 plaPRT participants. PRT significantly increased expression of genes involved in extracellular matrix remodeling pathways, and downregulated RNA processing pathways in both groups, however, metformin attenuated the number of differentially expressed genes within these pathways compared to plaPRT. Pathway analysis showed that genes unique to metPRT modulated aging-relevant pathways, such as cellular senescence and autophagy. Differentially expressed genes from baseline biopsies in older adults compared to resting muscle from young volunteers were reduced following PRT in plaPRT and were further reduced in metPRT. We suggest that although metformin may blunt pathways induced by PRT to promote muscle hypertrophy, adjunctive metformin during PRT may have beneficial effects on aging-associated pathways in muscle from older adults. Impact Journals 2020-10-18 /pmc/articles/PMC7655218/ /pubmed/33071237 http://dx.doi.org/10.18632/aging.104096 Text en Copyright: © 2020 Kulkarni et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Priority Research Paper Kulkarni, Ameya S. Peck, Bailey D. Walton, R. Grace Kern, Philip A. Mar, Jessica C. Windham, Samuel T. Bamman, Marcas M. Barzilai, Nir Peterson, Charlotte A. Metformin alters skeletal muscle transcriptome adaptations to resistance training in older adults |
title | Metformin alters skeletal muscle transcriptome adaptations to resistance training in older adults |
title_full | Metformin alters skeletal muscle transcriptome adaptations to resistance training in older adults |
title_fullStr | Metformin alters skeletal muscle transcriptome adaptations to resistance training in older adults |
title_full_unstemmed | Metformin alters skeletal muscle transcriptome adaptations to resistance training in older adults |
title_short | Metformin alters skeletal muscle transcriptome adaptations to resistance training in older adults |
title_sort | metformin alters skeletal muscle transcriptome adaptations to resistance training in older adults |
topic | Priority Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7655218/ https://www.ncbi.nlm.nih.gov/pubmed/33071237 http://dx.doi.org/10.18632/aging.104096 |
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