Muscle IGF-1-Induced Skeletal Muscle Hypertrophy Evokes Higher Insulin Sensitivity and Carbohydrate Use as Preferential Energy Substrate

We characterized the metabolic profile of transgenic mice exhibiting enhanced muscle mass driven by increased mIGF-1 expression (MLC/mIGF-1). As expected, 6-month-old MLC/mIGF-1 mice were heavier than age-matched wild type (WT) mice (37.4 ± 0.3 versus 31.8 ± 0.6 g, resp.). MLC/mIGF-1 mice had higher...

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Main Authors: Marcelo Augusto Christoffolete, William Jose Silva, Gracielle Vieira Ramos, Mirella Ribeiro Bento, Monique Oliveira Costa, Miriam Oliveira Ribeiro, Maristela Mitiko Okamoto, Tania Helena Lohmann, Ubiratan Fabres Machado, Antonio Musarò, Anselmo Sigari Moriscot
Format: Article
Language:English
Published: Hindawi Limited 2015-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2015/282984
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spelling doaj-b2b0ebb298624f97a1adaff1a978172f2020-11-24T22:37:37ZengHindawi LimitedBioMed Research International2314-61332314-61412015-01-01201510.1155/2015/282984282984Muscle IGF-1-Induced Skeletal Muscle Hypertrophy Evokes Higher Insulin Sensitivity and Carbohydrate Use as Preferential Energy SubstrateMarcelo Augusto Christoffolete0William Jose Silva1Gracielle Vieira Ramos2Mirella Ribeiro Bento3Monique Oliveira Costa4Miriam Oliveira Ribeiro5Maristela Mitiko Okamoto6Tania Helena Lohmann7Ubiratan Fabres Machado8Antonio Musarò9Anselmo Sigari Moriscot10Department of Anatomy, Institute of Biomedical Sciences, University of São Paulo, 05508-000 São Paulo, SP, BrazilDepartment of Anatomy, Institute of Biomedical Sciences, University of São Paulo, 05508-000 São Paulo, SP, BrazilDepartment of Anatomy, Institute of Biomedical Sciences, University of São Paulo, 05508-000 São Paulo, SP, BrazilDepartment of Anatomy, Institute of Biomedical Sciences, University of São Paulo, 05508-000 São Paulo, SP, BrazilDepartment of Anatomy, Institute of Biomedical Sciences, University of São Paulo, 05508-000 São Paulo, SP, BrazilBiological and Health Science Center, Mackenzie Presbyterian University, 01302-907 São Paulo, SP, BrazilDepartment of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, 05508-000 São Paulo, SP, BrazilDepartment of Anatomy, Institute of Biomedical Sciences, University of São Paulo, 05508-000 São Paulo, SP, BrazilDepartment of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, 05508-000 São Paulo, SP, BrazilInstitute Pasteur Cenci Bolognetti, DAHFMO, Unit of Histology and Medical Embryology, IIM, Sapienza University of Rome, 00161 Rome, ItalyDepartment of Anatomy, Institute of Biomedical Sciences, University of São Paulo, 05508-000 São Paulo, SP, BrazilWe characterized the metabolic profile of transgenic mice exhibiting enhanced muscle mass driven by increased mIGF-1 expression (MLC/mIGF-1). As expected, 6-month-old MLC/mIGF-1 mice were heavier than age-matched wild type (WT) mice (37.4 ± 0.3 versus 31.8 ± 0.6 g, resp.). MLC/mIGF-1 mice had higher respiratory quotient when compared to WT (0.9 ± 0.03 versus 0.74 ± 0.02, resp.) suggesting a preference for carbohydrate as the major fuel source. MLC/mIGF-1 mice had a higher rate of glucose disposal when compared to WT (3.25 ± 0.14 versus 2.39 ± 0.03%/min, resp.). The higher disposal rate correlated to ∼2-fold higher GLUT4 content in the extensor digitorum longus (EDL) muscle. Analysis of mRNA content for the glycolysis-related gene PFK-1 showed ∼3-fold upregulation in MLC/mIGF-1 animals. We also found a 50% downregulation of PGC1α mRNA levels in MLC/mIGF-1 mouse EDL muscle, suggesting less abundant mitochondria in this tissue. We found no difference in the expression of PPARα and PPARβ/δ, suggesting no modulation of key elements in oxidative metabolism. These data together suggest a shift in metabolism towards higher carbohydrate utilization, and that could explain the increased insulin sensitivity of hypertrophied skeletal muscle in MLC/mIGF-1 mice.http://dx.doi.org/10.1155/2015/282984
collection DOAJ
language English
format Article
sources DOAJ
author Marcelo Augusto Christoffolete
William Jose Silva
Gracielle Vieira Ramos
Mirella Ribeiro Bento
Monique Oliveira Costa
Miriam Oliveira Ribeiro
Maristela Mitiko Okamoto
Tania Helena Lohmann
Ubiratan Fabres Machado
Antonio Musarò
Anselmo Sigari Moriscot
spellingShingle Marcelo Augusto Christoffolete
William Jose Silva
Gracielle Vieira Ramos
Mirella Ribeiro Bento
Monique Oliveira Costa
Miriam Oliveira Ribeiro
Maristela Mitiko Okamoto
Tania Helena Lohmann
Ubiratan Fabres Machado
Antonio Musarò
Anselmo Sigari Moriscot
Muscle IGF-1-Induced Skeletal Muscle Hypertrophy Evokes Higher Insulin Sensitivity and Carbohydrate Use as Preferential Energy Substrate
BioMed Research International
author_facet Marcelo Augusto Christoffolete
William Jose Silva
Gracielle Vieira Ramos
Mirella Ribeiro Bento
Monique Oliveira Costa
Miriam Oliveira Ribeiro
Maristela Mitiko Okamoto
Tania Helena Lohmann
Ubiratan Fabres Machado
Antonio Musarò
Anselmo Sigari Moriscot
author_sort Marcelo Augusto Christoffolete
title Muscle IGF-1-Induced Skeletal Muscle Hypertrophy Evokes Higher Insulin Sensitivity and Carbohydrate Use as Preferential Energy Substrate
title_short Muscle IGF-1-Induced Skeletal Muscle Hypertrophy Evokes Higher Insulin Sensitivity and Carbohydrate Use as Preferential Energy Substrate
title_full Muscle IGF-1-Induced Skeletal Muscle Hypertrophy Evokes Higher Insulin Sensitivity and Carbohydrate Use as Preferential Energy Substrate
title_fullStr Muscle IGF-1-Induced Skeletal Muscle Hypertrophy Evokes Higher Insulin Sensitivity and Carbohydrate Use as Preferential Energy Substrate
title_full_unstemmed Muscle IGF-1-Induced Skeletal Muscle Hypertrophy Evokes Higher Insulin Sensitivity and Carbohydrate Use as Preferential Energy Substrate
title_sort muscle igf-1-induced skeletal muscle hypertrophy evokes higher insulin sensitivity and carbohydrate use as preferential energy substrate
publisher Hindawi Limited
series BioMed Research International
issn 2314-6133
2314-6141
publishDate 2015-01-01
description We characterized the metabolic profile of transgenic mice exhibiting enhanced muscle mass driven by increased mIGF-1 expression (MLC/mIGF-1). As expected, 6-month-old MLC/mIGF-1 mice were heavier than age-matched wild type (WT) mice (37.4 ± 0.3 versus 31.8 ± 0.6 g, resp.). MLC/mIGF-1 mice had higher respiratory quotient when compared to WT (0.9 ± 0.03 versus 0.74 ± 0.02, resp.) suggesting a preference for carbohydrate as the major fuel source. MLC/mIGF-1 mice had a higher rate of glucose disposal when compared to WT (3.25 ± 0.14 versus 2.39 ± 0.03%/min, resp.). The higher disposal rate correlated to ∼2-fold higher GLUT4 content in the extensor digitorum longus (EDL) muscle. Analysis of mRNA content for the glycolysis-related gene PFK-1 showed ∼3-fold upregulation in MLC/mIGF-1 animals. We also found a 50% downregulation of PGC1α mRNA levels in MLC/mIGF-1 mouse EDL muscle, suggesting less abundant mitochondria in this tissue. We found no difference in the expression of PPARα and PPARβ/δ, suggesting no modulation of key elements in oxidative metabolism. These data together suggest a shift in metabolism towards higher carbohydrate utilization, and that could explain the increased insulin sensitivity of hypertrophied skeletal muscle in MLC/mIGF-1 mice.
url http://dx.doi.org/10.1155/2015/282984
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