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Time-restricted feeding restores muscle function in Drosophila models of obesity and circadian-rhythm disruption

Pathological obesity can result from genetic predisposition, obesogenic diet, and circadian rhythm disruption. Obesity compromises function of muscle, which accounts for a majority of body mass. Behavioral intervention that can counteract obesity arising from genetic, diet or circadian disruption an...

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Autores principales: Villanueva, Jesús E., Livelo, Christopher, Trujillo, Adriana S., Chandran, Sahaana, Woodworth, Brendon, Andrade, Leo, Le, Hiep D., Manor, Uri, Panda, Satchidananda, Melkani, Girish C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6586848/
https://www.ncbi.nlm.nih.gov/pubmed/31221967
http://dx.doi.org/10.1038/s41467-019-10563-9
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author Villanueva, Jesús E.
Livelo, Christopher
Trujillo, Adriana S.
Chandran, Sahaana
Woodworth, Brendon
Andrade, Leo
Le, Hiep D.
Manor, Uri
Panda, Satchidananda
Melkani, Girish C.
author_facet Villanueva, Jesús E.
Livelo, Christopher
Trujillo, Adriana S.
Chandran, Sahaana
Woodworth, Brendon
Andrade, Leo
Le, Hiep D.
Manor, Uri
Panda, Satchidananda
Melkani, Girish C.
author_sort Villanueva, Jesús E.
collection PubMed
description Pathological obesity can result from genetic predisposition, obesogenic diet, and circadian rhythm disruption. Obesity compromises function of muscle, which accounts for a majority of body mass. Behavioral intervention that can counteract obesity arising from genetic, diet or circadian disruption and can improve muscle function holds untapped potential to combat the obesity epidemic. Here we show that Drosophila melanogaster (fruit fly) subject to obesogenic challenges exhibits metabolic disease phenotypes in skeletal muscle; sarcomere disorganization, mitochondrial deformation, upregulation of Phospho-AKT level, aberrant intramuscular lipid infiltration, and insulin resistance. Imposing time-restricted feeding (TRF) paradigm in which flies were fed for 12 h during the day counteracts obesity-induced dysmetabolism and improves muscle performance by suppressing intramuscular fat deposits, Phospho-AKT level, mitochondrial aberrations, and markers of insulin resistance. Importantly, TRF was effective even in an irregular lighting schedule mimicking shiftwork. Hence, TRF is an effective dietary intervention for combating metabolic dysfunction arising from multiple causes.
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spelling pubmed-65868482019-06-24 Time-restricted feeding restores muscle function in Drosophila models of obesity and circadian-rhythm disruption Villanueva, Jesús E. Livelo, Christopher Trujillo, Adriana S. Chandran, Sahaana Woodworth, Brendon Andrade, Leo Le, Hiep D. Manor, Uri Panda, Satchidananda Melkani, Girish C. Nat Commun Article Pathological obesity can result from genetic predisposition, obesogenic diet, and circadian rhythm disruption. Obesity compromises function of muscle, which accounts for a majority of body mass. Behavioral intervention that can counteract obesity arising from genetic, diet or circadian disruption and can improve muscle function holds untapped potential to combat the obesity epidemic. Here we show that Drosophila melanogaster (fruit fly) subject to obesogenic challenges exhibits metabolic disease phenotypes in skeletal muscle; sarcomere disorganization, mitochondrial deformation, upregulation of Phospho-AKT level, aberrant intramuscular lipid infiltration, and insulin resistance. Imposing time-restricted feeding (TRF) paradigm in which flies were fed for 12 h during the day counteracts obesity-induced dysmetabolism and improves muscle performance by suppressing intramuscular fat deposits, Phospho-AKT level, mitochondrial aberrations, and markers of insulin resistance. Importantly, TRF was effective even in an irregular lighting schedule mimicking shiftwork. Hence, TRF is an effective dietary intervention for combating metabolic dysfunction arising from multiple causes. Nature Publishing Group UK 2019-06-20 /pmc/articles/PMC6586848/ /pubmed/31221967 http://dx.doi.org/10.1038/s41467-019-10563-9 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Villanueva, Jesús E.
Livelo, Christopher
Trujillo, Adriana S.
Chandran, Sahaana
Woodworth, Brendon
Andrade, Leo
Le, Hiep D.
Manor, Uri
Panda, Satchidananda
Melkani, Girish C.
Time-restricted feeding restores muscle function in Drosophila models of obesity and circadian-rhythm disruption
title Time-restricted feeding restores muscle function in Drosophila models of obesity and circadian-rhythm disruption
title_full Time-restricted feeding restores muscle function in Drosophila models of obesity and circadian-rhythm disruption
title_fullStr Time-restricted feeding restores muscle function in Drosophila models of obesity and circadian-rhythm disruption
title_full_unstemmed Time-restricted feeding restores muscle function in Drosophila models of obesity and circadian-rhythm disruption
title_short Time-restricted feeding restores muscle function in Drosophila models of obesity and circadian-rhythm disruption
title_sort time-restricted feeding restores muscle function in drosophila models of obesity and circadian-rhythm disruption
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6586848/
https://www.ncbi.nlm.nih.gov/pubmed/31221967
http://dx.doi.org/10.1038/s41467-019-10563-9
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