Effects of leucine supplementation and resistance exercise on dexamethasone-induced muscle atrophy and insulin resistance in rats

Detalhes bibliográficos
Autor(a) principal: Nicastro, Humberto
Data de Publicação: 2012
Outros Autores: Zanchi, Nelo Eidy, Luz, Claudia Ribeiro da, Moraes, Wilson Max Almeida Monteiro de, Ramona, Pamella, Siqueira Filho, Mario Alves de, Chaves, Daniela Fojo Seixas, Medeiros, Alessandra [UNIFESP], Brum, Patricia Chakur, Dardevet, Dominique, Lancha Junior, Antonio Herbert
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1016/j.nut.2011.08.008
http://repositorio.unifesp.br/handle/11600/34723
Resumo: Objective: We aimed to evaluate the effects of resistance exercise (RE) and leucine (LEU) supplementation on dexamethasone (DEXA)-induced muscle atrophy and insulin resistance.Methods: Male Wistar rats were randomly divided into DEXA(DEX), DEXA + RE (DEX-RE), DEXA + LEU (DEX-LEU), and DEXA + RE + LEU (DEX-RE-LEU) groups. Each group received DEXA 5 mg . kg(-1) . d(-1) for 7 d from drinking water and were pair-fed to the DEX group; LEU-supplemented groups received 0.135 g . kg(-1) . d(-1) through gavage for 7 d; the RE protocol was based on three sessions of squat-type exercise composed by three sets of 10 repetitions at 70% of maximal voluntary strength capacity.Results: the plantaris mass was significantly greater in both trained groups compared with the non-trained groups. Muscle cross-sectional area and fiber areas did not differ between groups. Both trained groups displayed significant increases in the number of intermediated fibers (IIa/IIx), a decreased number of fast-twitch fibers (IIb), an increased ratio of the proteins phospho(Ser2448)/ total mammalian target of rapamycin and phospho(Thr389)/total 70-kDa ribosomal protein S6 kinase. and a decreased ratio of phospho(Ser253)/total Forkhead box protein-3a. Plasma glucose was significantly increased in the DEX-LEU group compared with the DEX group and RE significantly decreased hyperglycemia. the DEX-LEU group displayed decreased glucose transporter-4 translocation compared with the DEX group and RE restored this response. LEU supplementation worsened insulin sensitivity and did not attenuate muscle wasting in rats treated with DEXA. Conversely, RE modulated glucose homeostasis and fiber type transition in the plantaris muscle.Conclusion: Resistance exercise but not LEU supplementation promoted fiber type transition and improved glucose homeostasis in DEXA-treated rats. (C) 2012 Elsevier Inc. All rights reserved.
id UFSP_99a82f3fc5730d3acbf55f7258715434
oai_identifier_str oai:repositorio.unifesp.br/:11600/34723
network_acronym_str UFSP
network_name_str Repositório Institucional da UNIFESP
repository_id_str 3465
spelling Effects of leucine supplementation and resistance exercise on dexamethasone-induced muscle atrophy and insulin resistance in ratsBranched-chain amino acidsGlucose transporter-4Muscle wastingMammalian target of rapamycinGlucocorticoidObjective: We aimed to evaluate the effects of resistance exercise (RE) and leucine (LEU) supplementation on dexamethasone (DEXA)-induced muscle atrophy and insulin resistance.Methods: Male Wistar rats were randomly divided into DEXA(DEX), DEXA + RE (DEX-RE), DEXA + LEU (DEX-LEU), and DEXA + RE + LEU (DEX-RE-LEU) groups. Each group received DEXA 5 mg . kg(-1) . d(-1) for 7 d from drinking water and were pair-fed to the DEX group; LEU-supplemented groups received 0.135 g . kg(-1) . d(-1) through gavage for 7 d; the RE protocol was based on three sessions of squat-type exercise composed by three sets of 10 repetitions at 70% of maximal voluntary strength capacity.Results: the plantaris mass was significantly greater in both trained groups compared with the non-trained groups. Muscle cross-sectional area and fiber areas did not differ between groups. Both trained groups displayed significant increases in the number of intermediated fibers (IIa/IIx), a decreased number of fast-twitch fibers (IIb), an increased ratio of the proteins phospho(Ser2448)/ total mammalian target of rapamycin and phospho(Thr389)/total 70-kDa ribosomal protein S6 kinase. and a decreased ratio of phospho(Ser253)/total Forkhead box protein-3a. Plasma glucose was significantly increased in the DEX-LEU group compared with the DEX group and RE significantly decreased hyperglycemia. the DEX-LEU group displayed decreased glucose transporter-4 translocation compared with the DEX group and RE restored this response. LEU supplementation worsened insulin sensitivity and did not attenuate muscle wasting in rats treated with DEXA. Conversely, RE modulated glucose homeostasis and fiber type transition in the plantaris muscle.Conclusion: Resistance exercise but not LEU supplementation promoted fiber type transition and improved glucose homeostasis in DEXA-treated rats. (C) 2012 Elsevier Inc. All rights reserved.Univ São Paulo, Lab Appl Nutr & Metab, Sch Phys Educ & Sports, São Paulo, BrazilUniv São Paulo, Inst Biomed Sci, São Paulo, BrazilUniv São Paulo, Lab Mol & Cellular Physiol Exercise, Sch Phys Educ & Sports, São Paulo, BrazilUniv São Paulo, Sch Med, Lab Expt Hypertens, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Biosci, São Paulo, BrazilClermont Univ, UFR Med, UMR Nutr Humaine 1019, Clermont Ferrand, FranceINRA, UMR Unite Nutr Humaine 1019, F-63122 St Genes Champanelle, FranceUniversidade Federal de São Paulo, Dept Biosci, São Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)FAPESP: 08/51090-1FAPESP: 10/07062-3FAPESP: 10/10852-6FAPESP: 11/04690-6Elsevier B.V.Universidade de São Paulo (USP)Universidade Federal de São Paulo (UNIFESP)Clermont UnivINRANicastro, HumbertoZanchi, Nelo EidyLuz, Claudia Ribeiro daMoraes, Wilson Max Almeida Monteiro deRamona, PamellaSiqueira Filho, Mario Alves deChaves, Daniela Fojo SeixasMedeiros, Alessandra [UNIFESP]Brum, Patricia ChakurDardevet, DominiqueLancha Junior, Antonio Herbert2016-01-24T14:26:59Z2016-01-24T14:26:59Z2012-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion465-471application/pdfhttp://dx.doi.org/10.1016/j.nut.2011.08.008Nutrition. New York: Elsevier B.V., v. 28, n. 4, p. 465-471, 2012.10.1016/j.nut.2011.08.008WOS000302395800020.pdf0899-9007http://repositorio.unifesp.br/handle/11600/34723WOS:000302395800020engNutritioninfo:eu-repo/semantics/openAccesshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policyreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-08T11:36:53Zoai:repositorio.unifesp.br/:11600/34723Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-08T11:36:53Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Effects of leucine supplementation and resistance exercise on dexamethasone-induced muscle atrophy and insulin resistance in rats
title Effects of leucine supplementation and resistance exercise on dexamethasone-induced muscle atrophy and insulin resistance in rats
spellingShingle Effects of leucine supplementation and resistance exercise on dexamethasone-induced muscle atrophy and insulin resistance in rats
Nicastro, Humberto
Branched-chain amino acids
Glucose transporter-4
Muscle wasting
Mammalian target of rapamycin
Glucocorticoid
title_short Effects of leucine supplementation and resistance exercise on dexamethasone-induced muscle atrophy and insulin resistance in rats
title_full Effects of leucine supplementation and resistance exercise on dexamethasone-induced muscle atrophy and insulin resistance in rats
title_fullStr Effects of leucine supplementation and resistance exercise on dexamethasone-induced muscle atrophy and insulin resistance in rats
title_full_unstemmed Effects of leucine supplementation and resistance exercise on dexamethasone-induced muscle atrophy and insulin resistance in rats
title_sort Effects of leucine supplementation and resistance exercise on dexamethasone-induced muscle atrophy and insulin resistance in rats
author Nicastro, Humberto
author_facet Nicastro, Humberto
Zanchi, Nelo Eidy
Luz, Claudia Ribeiro da
Moraes, Wilson Max Almeida Monteiro de
Ramona, Pamella
Siqueira Filho, Mario Alves de
Chaves, Daniela Fojo Seixas
Medeiros, Alessandra [UNIFESP]
Brum, Patricia Chakur
Dardevet, Dominique
Lancha Junior, Antonio Herbert
author_role author
author2 Zanchi, Nelo Eidy
Luz, Claudia Ribeiro da
Moraes, Wilson Max Almeida Monteiro de
Ramona, Pamella
Siqueira Filho, Mario Alves de
Chaves, Daniela Fojo Seixas
Medeiros, Alessandra [UNIFESP]
Brum, Patricia Chakur
Dardevet, Dominique
Lancha Junior, Antonio Herbert
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Universidade Federal de São Paulo (UNIFESP)
Clermont Univ
INRA
dc.contributor.author.fl_str_mv Nicastro, Humberto
Zanchi, Nelo Eidy
Luz, Claudia Ribeiro da
Moraes, Wilson Max Almeida Monteiro de
Ramona, Pamella
Siqueira Filho, Mario Alves de
Chaves, Daniela Fojo Seixas
Medeiros, Alessandra [UNIFESP]
Brum, Patricia Chakur
Dardevet, Dominique
Lancha Junior, Antonio Herbert
dc.subject.por.fl_str_mv Branched-chain amino acids
Glucose transporter-4
Muscle wasting
Mammalian target of rapamycin
Glucocorticoid
topic Branched-chain amino acids
Glucose transporter-4
Muscle wasting
Mammalian target of rapamycin
Glucocorticoid
description Objective: We aimed to evaluate the effects of resistance exercise (RE) and leucine (LEU) supplementation on dexamethasone (DEXA)-induced muscle atrophy and insulin resistance.Methods: Male Wistar rats were randomly divided into DEXA(DEX), DEXA + RE (DEX-RE), DEXA + LEU (DEX-LEU), and DEXA + RE + LEU (DEX-RE-LEU) groups. Each group received DEXA 5 mg . kg(-1) . d(-1) for 7 d from drinking water and were pair-fed to the DEX group; LEU-supplemented groups received 0.135 g . kg(-1) . d(-1) through gavage for 7 d; the RE protocol was based on three sessions of squat-type exercise composed by three sets of 10 repetitions at 70% of maximal voluntary strength capacity.Results: the plantaris mass was significantly greater in both trained groups compared with the non-trained groups. Muscle cross-sectional area and fiber areas did not differ between groups. Both trained groups displayed significant increases in the number of intermediated fibers (IIa/IIx), a decreased number of fast-twitch fibers (IIb), an increased ratio of the proteins phospho(Ser2448)/ total mammalian target of rapamycin and phospho(Thr389)/total 70-kDa ribosomal protein S6 kinase. and a decreased ratio of phospho(Ser253)/total Forkhead box protein-3a. Plasma glucose was significantly increased in the DEX-LEU group compared with the DEX group and RE significantly decreased hyperglycemia. the DEX-LEU group displayed decreased glucose transporter-4 translocation compared with the DEX group and RE restored this response. LEU supplementation worsened insulin sensitivity and did not attenuate muscle wasting in rats treated with DEXA. Conversely, RE modulated glucose homeostasis and fiber type transition in the plantaris muscle.Conclusion: Resistance exercise but not LEU supplementation promoted fiber type transition and improved glucose homeostasis in DEXA-treated rats. (C) 2012 Elsevier Inc. All rights reserved.
publishDate 2012
dc.date.none.fl_str_mv 2012-04-01
2016-01-24T14:26:59Z
2016-01-24T14:26:59Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.nut.2011.08.008
Nutrition. New York: Elsevier B.V., v. 28, n. 4, p. 465-471, 2012.
10.1016/j.nut.2011.08.008
WOS000302395800020.pdf
0899-9007
http://repositorio.unifesp.br/handle/11600/34723
WOS:000302395800020
url http://dx.doi.org/10.1016/j.nut.2011.08.008
http://repositorio.unifesp.br/handle/11600/34723
identifier_str_mv Nutrition. New York: Elsevier B.V., v. 28, n. 4, p. 465-471, 2012.
10.1016/j.nut.2011.08.008
WOS000302395800020.pdf
0899-9007
WOS:000302395800020
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Nutrition
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
eu_rights_str_mv openAccess
rights_invalid_str_mv http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.format.none.fl_str_mv 465-471
application/pdf
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
_version_ 1814268289129381888