β-Hydroxy-β-methylbutyrate (HMβ) supplementation stimulates skeletal muscle hypertrophy in rats via the mTOR pathway

被引:0
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作者
Gustavo D Pimentel
José C Rosa
Fábio S Lira
Nelo E Zanchi
Eduardo R Ropelle
Lila M Oyama
Cláudia M Oller do Nascimento
Marco Túlio de Mello
Sergio Tufik
Ronaldo VT Santos
机构
[1] Federal University of São Paulo (UNIFESP),Department of Physiology of Nutrition
[2] State University of Campinas (UNICAMP),Department of Internal Medicine, FCM
[3] University of São Paulo (USP),Department of Cell Biology and Development, Molecular Cell Biology Study Group
[4] State University of Campinas (UNICAMP), Institute o Biomedical Sciences I
[5] Federal University of São Paulo (UNIFESP),Faculty of Applied Sciences
[6] Federal University of São Paulo (UNIFESP),Psychobiology & Biosciences
来源
Nutrition & Metabolism | / 8卷
关键词
Corticosterone; Insulin Signalling; Extensor Digitorum Longus; Corticosterone Level; Skeletal Muscle Mass;
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学科分类号
摘要
β-Hydroxy-β-methylbutyrate (HMβ) supplementation is used to treat cancer, sepsis and exercise-induced muscle damage. However, its effects on animal and human health and the consequences of this treatment in other tissues (e.g., fat and liver) have not been examined. The purpose of this study was to evaluate the effects of HMβ supplementation on skeletal muscle hypertrophy and the expression of proteins involved in insulin signalling. Rats were treated with HMβ (320 mg/kg body weight) or saline for one month. The skeletal muscle hypertrophy and insulin signalling were evaluated by western blotting, and hormonal concentrations were evaluated using ELISAs. HMβ supplementation induced muscle hypertrophy in the extensor digitorum longus (EDL) and soleus muscles and increased serum insulin levels, the expression of the mammalian target of rapamycin (mTOR) and phosphorylation of p70S6K in the EDL muscle. Expression of the insulin receptor was increased only in liver. Thus, our results suggest that HMβ supplementation can be used to increase muscle mass without adverse health effects.
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