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Functional effects of muscle PGC-1alpha in aged animals

PGC-1 (peroxisome-proliferator-activated receptor-γ coactivator-1) alpha is a potent transcriptional coactivator that coordinates the activation of numerous metabolic processes. Exercise strongly induces PGC-1alpha expression in muscle, and overexpression of PGC-1alpha in skeletal muscle activates m...

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Autores principales: Yang, Steven, Loro, Emanuele, Wada, Shogo, Kim, Boa, Tseng, Wei-Ju, Li, Kristina, Khurana, Tejvir S., Arany, Zoltan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7201623/
https://www.ncbi.nlm.nih.gov/pubmed/32375875
http://dx.doi.org/10.1186/s13395-020-00231-8
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author Yang, Steven
Loro, Emanuele
Wada, Shogo
Kim, Boa
Tseng, Wei-Ju
Li, Kristina
Khurana, Tejvir S.
Arany, Zoltan
author_facet Yang, Steven
Loro, Emanuele
Wada, Shogo
Kim, Boa
Tseng, Wei-Ju
Li, Kristina
Khurana, Tejvir S.
Arany, Zoltan
author_sort Yang, Steven
collection PubMed
description PGC-1 (peroxisome-proliferator-activated receptor-γ coactivator-1) alpha is a potent transcriptional coactivator that coordinates the activation of numerous metabolic processes. Exercise strongly induces PGC-1alpha expression in muscle, and overexpression of PGC-1alpha in skeletal muscle activates mitochondrial oxidative metabolism and neovascularization, leading to markedly increased endurance. In light of these findings, PGC-1alpha has been proposed to protect from age-associated sarcopenia, bone loss, and whole-body metabolic dysfunction, although these findings have been controversial. We therefore comprehensively evaluated muscle and whole-body function and metabolism in 24-month-old transgenic mice that over-express PGC-1alpha in skeletal muscle. We find that the powerful effects of PGC-1alpha on promoting muscle oxidative capacity and protection from muscle fatigability persist in aged animals, although at the expense of muscle strength. However, skeletal muscle PGC-1alpha does not prevent bone loss and in fact accentuates it, nor does it have long-term benefit on whole-body metabolic composition or insulin sensitivity. Protection from sarcopenia is seen in male animals with overexpression of PGC-1alpha in skeletal muscle but not in female animals. In summary, muscle-specific expression of PGC-1alpha into old age has beneficial effects on muscle fatigability and may protect from sarcopenia in males, but does not improve whole-body metabolism and appears to worsen age-related trabecular bone loss.
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spelling pubmed-72016232020-05-08 Functional effects of muscle PGC-1alpha in aged animals Yang, Steven Loro, Emanuele Wada, Shogo Kim, Boa Tseng, Wei-Ju Li, Kristina Khurana, Tejvir S. Arany, Zoltan Skelet Muscle Research PGC-1 (peroxisome-proliferator-activated receptor-γ coactivator-1) alpha is a potent transcriptional coactivator that coordinates the activation of numerous metabolic processes. Exercise strongly induces PGC-1alpha expression in muscle, and overexpression of PGC-1alpha in skeletal muscle activates mitochondrial oxidative metabolism and neovascularization, leading to markedly increased endurance. In light of these findings, PGC-1alpha has been proposed to protect from age-associated sarcopenia, bone loss, and whole-body metabolic dysfunction, although these findings have been controversial. We therefore comprehensively evaluated muscle and whole-body function and metabolism in 24-month-old transgenic mice that over-express PGC-1alpha in skeletal muscle. We find that the powerful effects of PGC-1alpha on promoting muscle oxidative capacity and protection from muscle fatigability persist in aged animals, although at the expense of muscle strength. However, skeletal muscle PGC-1alpha does not prevent bone loss and in fact accentuates it, nor does it have long-term benefit on whole-body metabolic composition or insulin sensitivity. Protection from sarcopenia is seen in male animals with overexpression of PGC-1alpha in skeletal muscle but not in female animals. In summary, muscle-specific expression of PGC-1alpha into old age has beneficial effects on muscle fatigability and may protect from sarcopenia in males, but does not improve whole-body metabolism and appears to worsen age-related trabecular bone loss. BioMed Central 2020-05-06 /pmc/articles/PMC7201623/ /pubmed/32375875 http://dx.doi.org/10.1186/s13395-020-00231-8 Text en © The Author(s) 2020 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Yang, Steven
Loro, Emanuele
Wada, Shogo
Kim, Boa
Tseng, Wei-Ju
Li, Kristina
Khurana, Tejvir S.
Arany, Zoltan
Functional effects of muscle PGC-1alpha in aged animals
title Functional effects of muscle PGC-1alpha in aged animals
title_full Functional effects of muscle PGC-1alpha in aged animals
title_fullStr Functional effects of muscle PGC-1alpha in aged animals
title_full_unstemmed Functional effects of muscle PGC-1alpha in aged animals
title_short Functional effects of muscle PGC-1alpha in aged animals
title_sort functional effects of muscle pgc-1alpha in aged animals
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7201623/
https://www.ncbi.nlm.nih.gov/pubmed/32375875
http://dx.doi.org/10.1186/s13395-020-00231-8
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