The role of resveratrol on skeletal muscle cell differentiation and myotube hypertrophy during glucose restriction

被引:0
|
作者
Hannah F. Dugdale
David C. Hughes
Robert Allan
Colleen S. Deane
Christopher R. Coxon
James P. Morton
Claire E. Stewart
Adam P. Sharples
机构
[1] Keele University,Institute for Science and Technology in Medicine (ISTM), School of Medicine
[2] Liverpool John Moores University,Stem Cells, Ageing and Molecular Physiology Research (SCAMP) Unit, Exercise Metabolism and Adaptation Research Group (EMARG), Research Institute for Sport and Exercise Sciences (RISES)
[3] University of Iowa,Department of Internal Medicine, Division of Endocrinology and Metabolism, Carver College of Medicine
[4] University of Central Lancashire,Centre for Applied Sport and Exercise Sciences
[5] University of Exeter,Department of Sport and Health Sciences, College of Life and Environmental Sciences
[6] Liverpool John Moores University,School of Pharmacy and Biomolecular Sciences
来源
Molecular and Cellular Biochemistry | 2018年 / 444卷
关键词
SIRT1; Dietary restriction; Myoblasts; Hypertrophy; Atrophy; MYHC; P70S6K; AMPK; MYHC;
D O I
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中图分类号
学科分类号
摘要
Glucose restriction (GR) impairs muscle cell differentiation and evokes myotube atrophy. Resveratrol treatment in skeletal muscle cells improves inflammatory-induced reductions in skeletal muscle cell differentiation. We therefore hypothesised that resveratrol treatment would improve muscle cell differentiation and myotube hypertrophy in differentiating C2C12 myoblasts and mature myotubes during GR. Glucose restriction at 0.6 g/L (3.3 mM) blocked differentiation and myotube hypertrophy versus high-glucose (4.5 g/L or 25 mM) differentiation media (DM) conditions universally used for myoblast culture. Resveratrol (10 µM) treatment increased SIRT1 phosphorylation in DM conditions, yet did not improve differentiation when administered to differentiating myoblasts in GR conditions. Resveratrol did evoke increases in hypertrophy of mature myotubes under DM conditions with corresponding elevated Igf-I and Myhc7 gene expression, coding for the ‘slow’ type I MYHC protein isoform. Inhibition of SIRT1 via EX-527 administration (100 nM) also reduced myotube diameter and area in DM conditions and resulted in lower gene expression of Myhc 1, 2 and 4 coding for ‘intermediate’ and ‘faster’ IIx, IIa and IIb protein isoforms, respectively. Resveratrol treatment did not appear to modulate phosphorylation of energy-sensing protein AMPK or protein translation initiator P70S6K. Importantly, in mature myotubes, resveratrol treatment was able to ameliorate reduced myotube growth in GR conditions over an acute 24-h period, but not over 48–72 h. Overall, resveratrol evoked myotube hypertrophy in DM conditions while favouring ‘slower’ Myhc gene expression and acutely ameliorated impaired myotube growth observed during glucose restriction.
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页码:109 / 123
页数:14
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