Effect of high-fat diet on the expression of proteins in muscle, adipose tissues, and liver of C57BL/6 mice

被引:97
作者
Schmid, GM
Converset, V
Walter, N
Sennitt, MV
Leung, KY
Byers, H
Ward, M
Hochstrasser, DF
Cawthorne, MA
Sanchez, JC
机构
[1] Univ Hosp Geneva, Biomed Proteom Res Grp, Cent Clin Chem Lab, CH-1211 Geneva 14, Switzerland
[2] Buckingham Univ, Clore Lab, Sch Sci, Buckingham, England
[3] Kings Coll London, S Wing Lab, Inst Psychiat, London WC2R 2LS, England
关键词
diet-induced obesity; differentially expressed proteins; insulin resistance; mice; type; 2; diabetes;
D O I
10.1002/pmic.200300810
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In the present study, the effect of a high fat diet on the expression of proteins in insulin target tissues was analyzed using a proteomic approach. Gastrocnemius muscle, white and brown adipose tissue, and liver were taken from C57BL/6 mice either fed on a high-fat or a chow diet. Expression levels of approximately 10 000 polypeptides for all the four tissues were assessed by two-dimensional gel electrophoresis (2-DE). Computer-assisted image analysis allowed the detection of 50 significantly (p < 0.05) differentially expressed proteins between obese and lean mice. Interestingly, more than half of these proteins were detected in the brown adipose tissue. The differentially expressed proteins were identified by tandem mass spectrometry. Several stress and redox proteins were modulated in response to the high-fat diet. A key glycolytic enzyme was found to be downregulated in adipose tissues and muscle, suggesting that at elevated plasma fatty acid concentrations, fatty acids compete with glucose as an oxidative fuel source. Furthermore, in brown adipose tissue there were significant changes in mitochondrial enzymes involved in the Krebs tricarboxylic acid (TCA) cycle and in the respiratory chain in response to the high-fat diet. The brown adipose tissue is an energy-dissipating tissue. Our data suggest that the high-fat diet treated mice were increasing energy expenditure to defend against weight gain.
引用
收藏
页码:2270 / 2282
页数:13
相关论文
共 71 条
[1]   Adipose tissue as an endocrine organ [J].
Ahima, RS ;
Flier, JS .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2000, 11 (08) :327-332
[2]   Melanie II - a third-generation software package for analysis of two-dimensional electrophoresis images: I. Features and user interface [J].
Appel, RD ;
Palagi, PM ;
Walther, D ;
Vargas, JR ;
Sanchez, JC ;
Ravier, F ;
Pasquali, C ;
Hochstrasser, DF .
ELECTROPHORESIS, 1997, 18 (15) :2724-2734
[3]   The adipocyte in insulin resistance: key molecules and the impact of the thiazolidinediones [J].
Arner, P .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2003, 14 (03) :137-145
[4]   ENZYMES OF GLUCOSE-METABOLISM AND OF CITRATE CLEAVAGE PATHWAY IN ADIPOSE-TISSUE OF NORMAL AND DIABETIC SUBJECTS [J].
BELFIORE, F ;
RABUAZZO, AM ;
NAPOLI, E ;
BORZI, V ;
LOVECCHIO, L .
DIABETES, 1975, 24 (10) :865-873
[5]   A NONLINEAR WIDE-RANGE IMMOBILIZED PH GRADIENT FOR 2-DIMENSIONAL ELECTROPHORESIS AND ITS DEFINITION IN A RELEVANT PH SCALE [J].
BJELLQVIST, B ;
PASQUALI, C ;
RAVIER, F ;
SANCHEZ, JC ;
HOCHSTRASSER, D .
ELECTROPHORESIS, 1993, 14 (12) :1357-1365
[6]   Interaction between free fatty acids and glucose metabolism [J].
Boden, G .
CURRENT OPINION IN CLINICAL NUTRITION AND METABOLIC CARE, 2002, 5 (05) :545-549
[7]   Long-term high-fat feeding leads to severe insulin resistance but not diabetes in Wistar rats [J].
Chalkley, SM ;
Hettiarachchi, M ;
Chisholm, DJ ;
Kraegen, EW .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2002, 282 (06) :E1231-E1238
[8]   Mitochondrial uncoupling:: Role of uncoupling protein anion carriers and relationship to thermogenesis and weight control "The benefits of losing control" [J].
Diehl, AM ;
Hoek, JB .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 1999, 31 (05) :493-506
[9]   Hepatic protein expression of lean mice and obese diabetic mice treated with peroxisome proliferator-activated receptor activators [J].
Edvardsson, U ;
von Löwenhielm, HB ;
Panfilov, O ;
Nyström, AC ;
Nilsson, F ;
Dahllöf, B .
PROTEOMICS, 2003, 3 (04) :468-478
[10]  
FELIG P, 1970, NEW ENGL J MED, V282, P166