Insulin resistance induced by physical inactivity is associated with multiple transcriptional changes in skeletal muscle in young men

被引:162
作者
Alibegovic, A. C. [1 ]
Sonne, M. P. [2 ]
Hojbjerre, L. [2 ]
Bork-Jensen, J. [1 ]
Jacobsen, S. [1 ]
Nilsson, E. [1 ]
Faerch, K. [1 ]
Hiscock, N. [3 ]
Mortensen, B. [1 ]
Friedrichsen, M. [1 ]
Stallknecht, B. [2 ]
Dela, F. [2 ]
Vaag, A. [1 ]
机构
[1] Steno Diabet Ctr, DK-2820 Gentofte, Denmark
[2] Univ Copenhagen, Fac Hlth Sci, Dept Biomed Sci, Ctr Healthy Ageing, Copenhagen, Denmark
[3] Unilever Discover Res & Dev, Sharnbrook, Beds, England
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2010年 / 299卷 / 05期
关键词
bed rest; peroxisome proliferator-activated receptor-gamma coactivator-1 alpha; gene expression; mitochondria; MESSENGER-RNA EXPRESSION; WHOLE-BODY LIPOLYSIS; BED REST; MITOCHONDRIAL RESPIRATION; EPITROCHLEARIS MUSCLE; DIABETES-MELLITUS; OXIDATIVE STRESS; CHRONIC DISEASE; BIRTH-WEIGHT; GLUT4; GENE;
D O I
10.1152/ajpendo.00590.2009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Alibegovic AC, Sonne MP, Hojbjerre L, Bork-Jensen J, Jacobsen S, Nilsson E, Faerch K, Hiscock N, Mortensen B, Friedrichsen M, Stallknecht B, Dela F, Vaag A. Insulin resistance induced by physical inactivity is associated with multiple transcriptional changes in skeletal muscle in young men. Am J Physiol Endocrinol Metab 299: E752-E763, 2010. First published August 24, 2010; doi: 10.1152/ajpendo.00590.2009.-Physical inactivity is a risk factor for insulin resistance. We examined the effect of 9 days of bed rest on basal and insulin-stimulated expression of genes potentially involved in insulin action by applying hypothesis-generating microarray in parallel with candidate gene real-time PCR approaches in 20 healthy young men. Furthermore, we investigated whether bed rest affected DNA methylation in the promoter region of the peroxisome proliferator-activated receptor-gamma coactivator-1 alpha (PPARGC1A) gene. Subjects were reexamined after 4 wk of retraining. We found that bed rest induced insulin resistance and altered the expression of more than 4,500 genes. These changes were only partly normalized after 4 wk of retraining. Pathway analyses revealed significant downregulation of 34 pathways, predominantly those of genes associated with mitochondrial function, including PPARGC1A. Despite induction of insulin resistance, bed rest resulted in a paradoxically increased response to acute insulin stimulation in the general expression of genes, particularly those involved in inflammation and endoplasmatic reticulum (ER) stress. Furthermore, bed rest changed gene expressions of several insulin resistance and diabetes candidate genes. We also observed a trend toward increased PPARGC1A DNA methylation after bed rest. We conclude that impaired expression of PPARGC1A and other genes involved in mitochondrial function as well as a paradoxically increased response to insulin of genes involved in inflammation and ER stress may contribute to the development of insulin resistance induced by bed rest. Lack of complete normalization of changes after 4 wk of retraining underscores the importance of maintaining a minimum of daily physical activity.
引用
收藏
页码:E752 / E763
页数:12
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