Gender Dimorphism in High-Fat-Diet-Induced Insulin Resistance in Skeletal Muscle of Aged Rats

被引:69
作者
Gomez-Perez, Yolanda [1 ]
Amengual-Cladera, Emilia [1 ]
Catala-Niell, Antoni [1 ]
Thomas-Moya, Elena [1 ]
Gianotti, Magdalena [1 ]
Maria Proenza, Ana [1 ]
Llado, Isabel [1 ]
机构
[1] Univ Illes Balears, Dept Biol Fonamental & Ciencies Salut, IUNICS, Grp Metab Energet & Nutr, Palma de Mallorca 07122, Spain
关键词
Obesity; Oxidative stress; Oxidative damage; GLUT4; UCP3; Adipokine;
D O I
10.1159/000185538
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Muscle resistance to insulin plays a key role in the metabolic dysregulation associated to obesity. A pro-inflammatory and pro-oxidant status has been proposed to be the link between dietary obesity and insulin resistance. Given the gender differences previously found in mitochondrial function and oxidative stress, the aim of the present study was to investigate whether this gender dimorphism leads to differences in the development of high-fat-diet-induced insulin resistance in rat skeletal muscle. Male and female rats of 15 months of age were fed with a high-fat-diet (32% fat) for 14 weeks. Control male rats showed a more marked insulin resistance status compared to females, as indicated by the glucose tolerance curve profile and the serum insulin, resistin and adiponectin levels. High-fat-diet feeding induced an excess of body weight of 16.2% in males and 38.4% in females, an increase in both muscle mitochondrial hydrogen peroxide production and in oxidative damage, together with a decrease in the Mn-superoxide dismutase activity in both genders. However, high-fat-diet fed female rats showed a less marked insulin resistance profile than males, higher mitochondrial oxygen consumption and cytochrome c oxidase activity, and a better capacity to counteract the oxidative-stress-dependent insulin resistance through an overexpression of both muscle UCP3 and GLUT4 proteins. These results point to a gender dimorphism in the insulin resistance status and in the response of skeletal muscle to high-fat-diet feeding which could be related to a more detrimental effect of age in male rats. Copyright (c) 2008 S. Karger AG, Basel
引用
收藏
页码:539 / 548
页数:10
相关论文
共 56 条
[1]  
AEBI H, 1984, METHOD ENZYMOL, V105, P121
[2]   Mitochondria from females exhibit higher antioxidant gene expression and lower oxidative damage than males [J].
Borrás, C ;
Sastre, J ;
García-Sala, D ;
Lloret, A ;
Pallardó, FV ;
Viña, J .
FREE RADICAL BIOLOGY AND MEDICINE, 2003, 34 (05) :546-552
[3]  
CARLBERG I, 1985, METHOD ENZYMOL, V113, P484
[4]   A high-fat diet leads to the progression of non-alcoholic fatty liver disease in obese rats [J].
Carmiel-Haggai, M ;
Cederbaum, AI ;
Nieto, N .
FASEB JOURNAL, 2004, 18 (14) :136-+
[5]   High-fat diet feeding elevates skeletal muscle uncoupling protein 3 levels but not its activity in rats [J].
Chou, CJ ;
Cha, MC ;
Jung, DW ;
Boozer, CN ;
Hashim, SA ;
Pi-Sunyer, FX .
OBESITY RESEARCH, 2001, 9 (05) :313-319
[6]   A MICROTITER PLATE ASSAY FOR CYTOCHROME-C-OXIDASE IN PERMEABILIZED WHOLE CELLS [J].
CHRZANOWSKALIGHTOWLERS, ZMA ;
TURNBULL, DM ;
LIGHTOWLERS, RN .
ANALYTICAL BIOCHEMISTRY, 1993, 214 (01) :45-49
[7]   Sexual dimorphism in cafeteria diet-induced hypertension is associated with gender-related difference in renal leptin receptor down-regulation [J].
Coatmellec-Taglioni, G ;
Dausse, JP ;
Giudicelli, Y ;
Ribière, C .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2003, 305 (01) :362-367
[8]   Skeletal muscle of female rats exhibit higher mitochondrial mass and oxidative-phosphorylative capacities compared to males [J].
Colom, Bartomeu ;
Alcolea, Maria Pilar ;
Valle, Adamo ;
Oliver, Jordi ;
Roca, Pilar ;
Garcia-Palmer, Francisco J. .
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2007, 19 (1-4) :205-212
[9]   Caloric restriction and gender modulate cardiac muscle mitochondrial H2O2 production and oxidative damage [J].
Colom, Bartomeu ;
Oliver, Jordi ;
Roca, Pilar ;
Garcia-Palmer, Francisco J. .
CARDIOVASCULAR RESEARCH, 2007, 74 (03) :456-465
[10]   Sexual differentiation, pregnancy, calorie restriction, and aging affect the adipocyte-specific secretory protein adiponectin [J].
Combs, TP ;
Berg, AH ;
Rajala, MW ;
Klebanov, S ;
Iyengar, P ;
Jimenez-Chillaron, JC ;
Patti, ME ;
Klein, SL ;
Weinstein, RS ;
Scherer, PE .
DIABETES, 2003, 52 (02) :268-276