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
相关论文
共 50 条
[1]   Insulin action in cultured human skeletal muscle cells during differentiation: assessment of cell surface GLUT4 and GLUT1 content [J].
Al-Khalili, L ;
Chibalin, AV ;
Kannisto, K ;
Zhang, BB ;
Permert, J ;
Holman, GD ;
Ehrenborg, E ;
Ding, VDH ;
Zierath, JR ;
Krook, A .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2003, 60 (05) :991-998
[2]   Increased rate of whole body lipolysis before and after 9 days of bed rest in healthy young men born with low birth weight [J].
Alibegovic, A. C. ;
Hojbjerre, L. ;
Sonne, M. P. ;
van Hall, G. ;
Alsted, T. J. ;
Kiens, B. ;
Stallknecht, B. ;
Dela, F. ;
Vaag, A. .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2010, 298 (03) :E555-E564
[3]   The T-Allele of TCF7L2 rs7903146 Associates With a Reduced Compensation of Insulin Secretion for Insulin Resistance Induced by 9 Days of Bed Rest [J].
Alibegovic, Amra C. ;
Sonne, Mette P. ;
Hojbjerre, Lise ;
Hansen, Torben ;
Pedersen, Oluf ;
van Hall, Gerrit ;
Holst, Jens J. ;
Stallknecht, Bente ;
Dela, Flemming ;
Vaag, Allan .
DIABETES, 2010, 59 (04) :836-843
[4]  
Alibegovic AC, 2009, DIABETES, V58, pA338
[5]   INCREASED EXPRESSION OF MITOCHONDRIAL-ENCODED GENES IN SKELETAL-MUSCLE OF HUMANS WITH DIABETES-MELLITUS [J].
ANTONETTI, DA ;
REYNET, C ;
KAHN, CR .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (03) :1383-1388
[6]   Transcriptional regulation of the GLUT4 gene:: from PPAR-γ and FOXO1 to FFA and inflammation [J].
Armoni, Michal ;
Harel, Chava ;
Karnieli, Eddy .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2007, 18 (03) :100-107
[7]   Adaptations of skeletal muscle to exercise: rapid increase in the transcriptional coactivator PGC-1 [J].
Baar, K ;
Wende, AR ;
Jones, TE ;
Marison, M ;
Nolte, LA ;
Chen, M ;
Kelly, DP ;
Holloszy, JO .
FASEB JOURNAL, 2002, 16 (14) :1879-1886
[8]   Non-CpG Methylation of the PGC-1α Promoter through DNMT3B Controls Mitochondrial Density [J].
Barres, Romain ;
Osler, Megan E. ;
Yan, Jie ;
Rune, Anna ;
Fritz, Tomas ;
Caidahl, Kenneth ;
Krook, Anna ;
Zierath, Juleen R. .
CELL METABOLISM, 2009, 10 (03) :189-198
[9]   Impaired mitochondrial substrate oxidation in muscle of insulin-resistant offspring of type 2 diabetic patients [J].
Befroy, Douglas E. ;
Petersen, Kitt Falk ;
Dufour, Sylvie ;
Mason, Graeme F. ;
de Graaf, Robin A. ;
Rothman, Douglas L. ;
Shulman, Gerald I. .
DIABETES, 2007, 56 (05) :1376-1381
[10]   Reduced physical activity and risk of chronic disease: the biology behind the consequences [J].
Booth, Frank W. ;
Laye, Matthew J. ;
Lees, Simon J. ;
Rector, R. Scott ;
Thyfault, John P. .
EUROPEAN JOURNAL OF APPLIED PHYSIOLOGY, 2008, 102 (04) :381-390