The stress response of the liver to physical exercise

被引:1
作者
Hoene, Miriam [1 ]
Weigert, Cora [1 ]
机构
[1] Univ Tubingen Hosp, Dept Internal Med, Div Endocrinol Diabetol Angiol Nephrol Pathobioch, Tubingen, Germany
关键词
MAPK; p53; energy depletion; oxidative stress; glucose output; ACTIVATED PROTEIN-KINASE; HEPATIC GLUCOSE-PRODUCTION; DENSITY-LIPOPROTEIN CHOLESTEROL; JUN NH2-TERMINAL KINASE; HUMAN SKELETAL-MUSCLE; FATTY-ACID SYNTHASE; BETA-CELL FUNCTION; OXIDATIVE STRESS; INSULIN SENSITIVITY; GENE-EXPRESSION;
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recent research on the effectiveness of training interventions indicates major alterations of hepatic lipid metabolism and suggests a substantial and beneficial adaptation of the liver to regular physical activity in humans. However, while various data demonstrate the response of the working skeletal muscle to acute exercise and training, considerably less is known about the molecular events in the liver during and after increased physical activity. Here we discuss recent studies performed in rodents, that elucidate the acute hepatic response to one single bout of exercise with particular emphasis on stress response-related pathways. The acute transcriptional response to one exercise bout comprises three-times more hepatic transcripts than those expressed in soleus muscle, with a significantly more pronounced up- or downregulation of hepatic genes. Evaluation of the affected pathways shows that the liver responds to acute exercise with a rapid activation of the mitogen-activated protein kinase (MAPK) signalling pathway, of the p53 protein, and of interleukin (IL)-6-type cytokine signalling pathways, resulting in a marked transcriptional upregulation of stress response genes (e.g. transcription factors of the Fos/Jun-family, growth arrest and DNA damage (GADD)45 gamma, and p53-target genes) and genes typically induced by energy depletion, e.g. insulin-like growth factor binding protein (IGFBP)-1 peroxisome proliferator-activated receptor coactivator (PGC)1 alpha. One explanation for the marked differential expression of hepatic genes immediately after exercise is the induction of energetic stress. After non-exhaustive exercise energy depletion predominantly occurs in the liver, not as much in the working muscle, and during exercise, the liver is exposed to altered concentrations of insulin and glucagon in the portal vein. Furthermore, lower plasma glucose levels post-exercise are related to. increased expression levels of stress response genes. It appears that the unique function of the liver to supply glucose for the working muscle renders this organ especially susceptible for exercise-induced cellular stress that leads to the marked induction of defense adaptations. These results give rise to the question whether these molecular events are linked not only to stress defense but to the metabolic adaptations of the liver to exercise.
引用
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页码:163 / 183
页数:21
相关论文
共 133 条
[81]   Influence of exercise duration on serum insulin-like growth factor and its binding proteins in athletes [J].
Nguyen, UN ;
Mougin, F ;
Simon-Rigaud, ML ;
Rouillon, JD ;
Marguet, P ;
Regnard, J .
EUROPEAN JOURNAL OF APPLIED PHYSIOLOGY AND OCCUPATIONAL PHYSIOLOGY, 1998, 78 (06) :533-537
[82]   Response and adaptation of skeletal muscle to exercise - the role of reactive oxygen species [J].
Niess, Andreas Michael ;
Simon, Perikles .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2007, 12 :4826-4838
[83]  
Northoff H, 2008, EXERC IMMUNOL REV, V14, P86
[84]   Exercise and the Treatment of Diabetes and Obesity [J].
O'Gorman, Donal J. ;
Krook, Anna .
ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA, 2008, 37 (04) :887-+
[85]   The effects of moderate, strenuous, and overtraining on oxidative stress markers and DNA repair in rat liver [J].
Ogonovszky, H ;
Sasvári, M ;
Dosek, A ;
Berkes, I ;
Kaneko, T ;
Tahara, S ;
Nakamoto, F ;
Goto, S ;
Radák, Z .
CANADIAN JOURNAL OF APPLIED PHYSIOLOGY-REVUE CANADIENNE DE PHYSIOLOGIE APPLIQUEE, 2005, 30 (02) :186-195
[86]   Activation of AMP-activated protein kinase induces p53-dependent apoptotic cell death in response to energetic stress [J].
Okoshi, Rintaro ;
Ozaki, Toshinori ;
Yamamoto, Hideki ;
Ando, Kiyohiro ;
Koida, Nami ;
Ono, Sayaka ;
Koda, Tadayuki ;
Kamijo, Takehiko ;
Nakagawara, Akira ;
Kizaki, Harutoshi .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (07) :3979-3987
[87]   The effect of exercise, training, and inactivity on insulin sensitivity in diabetics and their relatives:: what is new? [J].
Ostergard, Torben ;
Jessen, Niels ;
Schmitz, Ole ;
Mandarino, Lawrence J. .
APPLIED PHYSIOLOGY NUTRITION AND METABOLISM, 2007, 32 (03) :541-548
[88]   Coordinate regulation of malonyl-CoA decarboxylase, sn-glycerol-3-phosphate acyltransferase, and acetyl-CoA carboxylase by AMP-activated protein kinase in rat tissues in response to exercise [J].
Park, H ;
Kaushik, VK ;
Constant, S ;
Prentki, M ;
Przybytkowski, E ;
Ruderman, NB ;
Saha, AK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (36) :32571-32577
[89]   Exendin-4 and exercise promotes β-cell function and mass through IRS2 induction in islets of diabetic rats [J].
Park, Sunmin ;
Hong, Sang Mee ;
Sung, So Ra .
LIFE SCIENCES, 2008, 82 (9-10) :503-511
[90]   Dual-specificity phosphatases: critical regulators with diverse cellular targets [J].
Patterson, Kate I. ;
Brummer, Tilman ;
O'Brien, Philippa M. ;
Daly, Roger J. .
BIOCHEMICAL JOURNAL, 2009, 418 :475-489