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The consequences of a high-calorie diet background before calorie restriction on skeletal muscles in a mouse model

The beneficial effects of calorie restriction (CR) are numerous. However, there is no scientific evidence about how a high-calorie diet (HCD) background influences the mechanisms underlying CR on skeletal muscles in an experimental mouse model. Herein we present empirical evidence showing significan...

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Autores principales: Maldonado, Martin, Chen, Jianying, Lujun, Yang, Duan, Huiqin, Raja, Mazhar Ali, Qu, Ting, Huang, Tianhua, Gu, Jiang, Zhong, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8266348/
https://www.ncbi.nlm.nih.gov/pubmed/34166224
http://dx.doi.org/10.18632/aging.203237
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author Maldonado, Martin
Chen, Jianying
Lujun, Yang
Duan, Huiqin
Raja, Mazhar Ali
Qu, Ting
Huang, Tianhua
Gu, Jiang
Zhong, Ying
author_facet Maldonado, Martin
Chen, Jianying
Lujun, Yang
Duan, Huiqin
Raja, Mazhar Ali
Qu, Ting
Huang, Tianhua
Gu, Jiang
Zhong, Ying
author_sort Maldonado, Martin
collection PubMed
description The beneficial effects of calorie restriction (CR) are numerous. However, there is no scientific evidence about how a high-calorie diet (HCD) background influences the mechanisms underlying CR on skeletal muscles in an experimental mouse model. Herein we present empirical evidence showing significant interactions between HCD (4 months) and CR (3 months). Pectoralis major and quadriceps femoris vastus medialis, in the experimental and control groups, displayed metabolic and physiologic heterogeneity and remarkable plasticity, according to the dietary interventions. HCD-CR not only altered genetic activation patterns of satellite SC markers but also boosted the expression of myogenic regulatory factors and key activators of mitochondrial biogenesis, which in turn were also associated with metabolic fiber transition. Our data prompt us to theorize that the effects of CR may vary according to the physiologic, metabolic, and genetic peculiarities of the skeletal muscle described here and that INTM/IM lipid infiltration and tissue-specific fuel-energy status (demand/supply) both hold dependent-interacting roles with other key anti-aging mechanisms triggered by CR. Systematic integration of an HCD with CR appears to bring potential benefits for skeletal muscle function and energy metabolism. However, at this stage of our research, an optimal balance between the two dietary conditions, where anti-aging effects can be accomplished, is under intensive investigation in combination with other tissues and organs at different levels of organization within the organ system.
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spelling pubmed-82663482021-07-09 The consequences of a high-calorie diet background before calorie restriction on skeletal muscles in a mouse model Maldonado, Martin Chen, Jianying Lujun, Yang Duan, Huiqin Raja, Mazhar Ali Qu, Ting Huang, Tianhua Gu, Jiang Zhong, Ying Aging (Albany NY) Research Paper The beneficial effects of calorie restriction (CR) are numerous. However, there is no scientific evidence about how a high-calorie diet (HCD) background influences the mechanisms underlying CR on skeletal muscles in an experimental mouse model. Herein we present empirical evidence showing significant interactions between HCD (4 months) and CR (3 months). Pectoralis major and quadriceps femoris vastus medialis, in the experimental and control groups, displayed metabolic and physiologic heterogeneity and remarkable plasticity, according to the dietary interventions. HCD-CR not only altered genetic activation patterns of satellite SC markers but also boosted the expression of myogenic regulatory factors and key activators of mitochondrial biogenesis, which in turn were also associated with metabolic fiber transition. Our data prompt us to theorize that the effects of CR may vary according to the physiologic, metabolic, and genetic peculiarities of the skeletal muscle described here and that INTM/IM lipid infiltration and tissue-specific fuel-energy status (demand/supply) both hold dependent-interacting roles with other key anti-aging mechanisms triggered by CR. Systematic integration of an HCD with CR appears to bring potential benefits for skeletal muscle function and energy metabolism. However, at this stage of our research, an optimal balance between the two dietary conditions, where anti-aging effects can be accomplished, is under intensive investigation in combination with other tissues and organs at different levels of organization within the organ system. Impact Journals 2021-06-24 /pmc/articles/PMC8266348/ /pubmed/34166224 http://dx.doi.org/10.18632/aging.203237 Text en Copyright: © 2021 Maldonado 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 Research Paper
Maldonado, Martin
Chen, Jianying
Lujun, Yang
Duan, Huiqin
Raja, Mazhar Ali
Qu, Ting
Huang, Tianhua
Gu, Jiang
Zhong, Ying
The consequences of a high-calorie diet background before calorie restriction on skeletal muscles in a mouse model
title The consequences of a high-calorie diet background before calorie restriction on skeletal muscles in a mouse model
title_full The consequences of a high-calorie diet background before calorie restriction on skeletal muscles in a mouse model
title_fullStr The consequences of a high-calorie diet background before calorie restriction on skeletal muscles in a mouse model
title_full_unstemmed The consequences of a high-calorie diet background before calorie restriction on skeletal muscles in a mouse model
title_short The consequences of a high-calorie diet background before calorie restriction on skeletal muscles in a mouse model
title_sort consequences of a high-calorie diet background before calorie restriction on skeletal muscles in a mouse model
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8266348/
https://www.ncbi.nlm.nih.gov/pubmed/34166224
http://dx.doi.org/10.18632/aging.203237
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