High-fat diet suppresses the positive effect of creatine supplementation on skeletal muscle function by reducing protein expression of IGF-PI3K-AKT-mTOR pathway

Detalhes bibliográficos
Autor(a) principal: Ferretti, Renato [UNESP]
Data de Publicação: 2018
Outros Autores: Moura, Eliezer Guimaraes, Santos, Veridiana Carvalho dos [UNESP], Caldeira, Eduardo Jose, Conte, Marcelo, Matsumura, Cintia Yuri [UNESP], Pertille, Adriana, Mosqueira, Matias
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1371/journal.pone.0199728
http://hdl.handle.net/11449/184901
Resumo: High-fat (HF) diets in combination with sedentary lifestyle represent one of the major public health concerns predisposing to obesity and diabetes leading to skeletal muscle atrophy, decreased fiber diameter and muscle mass with accumulation of fat tissue resulting in loss of muscle strength. One strategy to overcome the maleficent effects of HF diet is resistance training, a strategy used to improve muscle mass, reverting the negative effects on obesity-related changes in skeletal muscle. Together with resistance training, supplementation with creatine monohydrate (CrM) in the diet has been used to improve muscle mass and strength. Creatine is a non-essential amino acid that is directly involved in the cross-bridge cycle providing a phosphate group to ADP during the initiation of muscle contraction. Besides its antioxidant and anti-inflammatory effects CrM also upregulates IGF-1 resulting in hyperthophy with an increase in muscle function. However, it is unknown whether CrM supplementation during resistance training would revert the negative effects of high-fat diet on the muscle performance. During 8 weeks we measured muscle performance to climb a 1.1m and 80 degrees ladder with increasing load on trained rats that had received standard diet or high-fat diet, supplemented or not with CrM. We observed that the CrM supplementation up-regulated IGF-1 and phospho-AKT protein levels, suggesting an activation of the IGF1P13K-Akt/PKB-mTOR pathway. Moreover, despite the CrM supplementation, HF diet downregulated several proteins of the IGF1-PI3K-Akt/PKB-mTOR pathway, suggesting that diet lipid content is crucial to maintain or improve muscle function during resistance training.
id UNSP_8ac725e3fbc702838313ce5723046a66
oai_identifier_str oai:repositorio.unesp.br:11449/184901
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling High-fat diet suppresses the positive effect of creatine supplementation on skeletal muscle function by reducing protein expression of IGF-PI3K-AKT-mTOR pathwayHigh-fat (HF) diets in combination with sedentary lifestyle represent one of the major public health concerns predisposing to obesity and diabetes leading to skeletal muscle atrophy, decreased fiber diameter and muscle mass with accumulation of fat tissue resulting in loss of muscle strength. One strategy to overcome the maleficent effects of HF diet is resistance training, a strategy used to improve muscle mass, reverting the negative effects on obesity-related changes in skeletal muscle. Together with resistance training, supplementation with creatine monohydrate (CrM) in the diet has been used to improve muscle mass and strength. Creatine is a non-essential amino acid that is directly involved in the cross-bridge cycle providing a phosphate group to ADP during the initiation of muscle contraction. Besides its antioxidant and anti-inflammatory effects CrM also upregulates IGF-1 resulting in hyperthophy with an increase in muscle function. However, it is unknown whether CrM supplementation during resistance training would revert the negative effects of high-fat diet on the muscle performance. During 8 weeks we measured muscle performance to climb a 1.1m and 80 degrees ladder with increasing load on trained rats that had received standard diet or high-fat diet, supplemented or not with CrM. We observed that the CrM supplementation up-regulated IGF-1 and phospho-AKT protein levels, suggesting an activation of the IGF1P13K-Akt/PKB-mTOR pathway. Moreover, despite the CrM supplementation, HF diet downregulated several proteins of the IGF1-PI3K-Akt/PKB-mTOR pathway, suggesting that diet lipid content is crucial to maintain or improve muscle function during resistance training.Sao Paulo State Univ UNESP, Inst Biosci Botucatu, Dept Anat, Botucatu, SP, BrazilCtr Univ Adventista Sao Paulo, Lab Phys Act Metab & Hlth, Sao Paulo, BrazilFMJ, Dept Morphol & Basic Pathol, Sao Paulo, BrazilESEF, Sao Paulo, BrazilUniv Metodista Piracicaba, Lab Neuromuscular Plast, Grad Program Sci Human Movement, Sao Paulo, BrazilHeidelberg Univ Hosp, Inst Physiol & Pathophysiol, Cardioventilatory Muscle Physiol Lab, Heidelberg, GermanySao Paulo State Univ UNESP, Inst Biosci Botucatu, Dept Anat, Botucatu, SP, BrazilPublic Library ScienceUniversidade Estadual Paulista (Unesp)Ctr Univ Adventista Sao PauloFMJESEFUniv Metodista PiracicabaHeidelberg Univ HospFerretti, Renato [UNESP]Moura, Eliezer GuimaraesSantos, Veridiana Carvalho dos [UNESP]Caldeira, Eduardo JoseConte, MarceloMatsumura, Cintia Yuri [UNESP]Pertille, AdrianaMosqueira, Matias2019-10-04T12:31:00Z2019-10-04T12:31:00Z2018-10-04info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article20http://dx.doi.org/10.1371/journal.pone.0199728Plos One. San Francisco: Public Library Science, v. 13, n. 10, 20 p., 2018.1932-6203http://hdl.handle.net/11449/18490110.1371/journal.pone.0199728WOS:000446383500001368161316008617581987719983474830000-0003-3944-19060000-0002-7237-7021Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPlos Oneinfo:eu-repo/semantics/openAccess2021-10-23T19:49:56Zoai:repositorio.unesp.br:11449/184901Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T20:36:44.346348Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv High-fat diet suppresses the positive effect of creatine supplementation on skeletal muscle function by reducing protein expression of IGF-PI3K-AKT-mTOR pathway
title High-fat diet suppresses the positive effect of creatine supplementation on skeletal muscle function by reducing protein expression of IGF-PI3K-AKT-mTOR pathway
spellingShingle High-fat diet suppresses the positive effect of creatine supplementation on skeletal muscle function by reducing protein expression of IGF-PI3K-AKT-mTOR pathway
Ferretti, Renato [UNESP]
title_short High-fat diet suppresses the positive effect of creatine supplementation on skeletal muscle function by reducing protein expression of IGF-PI3K-AKT-mTOR pathway
title_full High-fat diet suppresses the positive effect of creatine supplementation on skeletal muscle function by reducing protein expression of IGF-PI3K-AKT-mTOR pathway
title_fullStr High-fat diet suppresses the positive effect of creatine supplementation on skeletal muscle function by reducing protein expression of IGF-PI3K-AKT-mTOR pathway
title_full_unstemmed High-fat diet suppresses the positive effect of creatine supplementation on skeletal muscle function by reducing protein expression of IGF-PI3K-AKT-mTOR pathway
title_sort High-fat diet suppresses the positive effect of creatine supplementation on skeletal muscle function by reducing protein expression of IGF-PI3K-AKT-mTOR pathway
author Ferretti, Renato [UNESP]
author_facet Ferretti, Renato [UNESP]
Moura, Eliezer Guimaraes
Santos, Veridiana Carvalho dos [UNESP]
Caldeira, Eduardo Jose
Conte, Marcelo
Matsumura, Cintia Yuri [UNESP]
Pertille, Adriana
Mosqueira, Matias
author_role author
author2 Moura, Eliezer Guimaraes
Santos, Veridiana Carvalho dos [UNESP]
Caldeira, Eduardo Jose
Conte, Marcelo
Matsumura, Cintia Yuri [UNESP]
Pertille, Adriana
Mosqueira, Matias
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Ctr Univ Adventista Sao Paulo
FMJ
ESEF
Univ Metodista Piracicaba
Heidelberg Univ Hosp
dc.contributor.author.fl_str_mv Ferretti, Renato [UNESP]
Moura, Eliezer Guimaraes
Santos, Veridiana Carvalho dos [UNESP]
Caldeira, Eduardo Jose
Conte, Marcelo
Matsumura, Cintia Yuri [UNESP]
Pertille, Adriana
Mosqueira, Matias
description High-fat (HF) diets in combination with sedentary lifestyle represent one of the major public health concerns predisposing to obesity and diabetes leading to skeletal muscle atrophy, decreased fiber diameter and muscle mass with accumulation of fat tissue resulting in loss of muscle strength. One strategy to overcome the maleficent effects of HF diet is resistance training, a strategy used to improve muscle mass, reverting the negative effects on obesity-related changes in skeletal muscle. Together with resistance training, supplementation with creatine monohydrate (CrM) in the diet has been used to improve muscle mass and strength. Creatine is a non-essential amino acid that is directly involved in the cross-bridge cycle providing a phosphate group to ADP during the initiation of muscle contraction. Besides its antioxidant and anti-inflammatory effects CrM also upregulates IGF-1 resulting in hyperthophy with an increase in muscle function. However, it is unknown whether CrM supplementation during resistance training would revert the negative effects of high-fat diet on the muscle performance. During 8 weeks we measured muscle performance to climb a 1.1m and 80 degrees ladder with increasing load on trained rats that had received standard diet or high-fat diet, supplemented or not with CrM. We observed that the CrM supplementation up-regulated IGF-1 and phospho-AKT protein levels, suggesting an activation of the IGF1P13K-Akt/PKB-mTOR pathway. Moreover, despite the CrM supplementation, HF diet downregulated several proteins of the IGF1-PI3K-Akt/PKB-mTOR pathway, suggesting that diet lipid content is crucial to maintain or improve muscle function during resistance training.
publishDate 2018
dc.date.none.fl_str_mv 2018-10-04
2019-10-04T12:31:00Z
2019-10-04T12:31:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1371/journal.pone.0199728
Plos One. San Francisco: Public Library Science, v. 13, n. 10, 20 p., 2018.
1932-6203
http://hdl.handle.net/11449/184901
10.1371/journal.pone.0199728
WOS:000446383500001
3681613160086175
8198771998347483
0000-0003-3944-1906
0000-0002-7237-7021
url http://dx.doi.org/10.1371/journal.pone.0199728
http://hdl.handle.net/11449/184901
identifier_str_mv Plos One. San Francisco: Public Library Science, v. 13, n. 10, 20 p., 2018.
1932-6203
10.1371/journal.pone.0199728
WOS:000446383500001
3681613160086175
8198771998347483
0000-0003-3944-1906
0000-0002-7237-7021
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Plos One
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 20
dc.publisher.none.fl_str_mv Public Library Science
publisher.none.fl_str_mv Public Library Science
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
_version_ 1808129226813997056