Uncoupling protein 3 content is decreased in skeletal muscle of patients with type 2 diabetes

被引:87
作者
Schrauwen, P
Hesselink, MKC
Blaak, EE
Borghouts, LB
Schaart, G
Saris, WHM
Keizer, HA
机构
[1] Maastricht Univ, Dept Human Biol, Nutr & Toxicol Res Inst Maastricht, NL-6200 MD Maastricht, Netherlands
[2] Maastricht Univ, Dept Movement Sci, Maastricht, Netherlands
关键词
D O I
10.2337/diabetes.50.12.2870
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Recently, a role for uncoupling protein-3 (UCP3) in carbohydrate metabolism and in type 2 diabetes has been suggested. Mice overexpressing UCP3 in skeletal muscle showed reduced fasting plasma glucose levels, improved glucose tolerance after an oral glucose load, and reduced fasting plasma insulin levels. However, data regarding the expression of UCP3 in patients with type 2 diabetes is inconsistent, and so far, there have been no reports of UCP3 protein content. Here we compared, for the first time, the protein levels of UCP3 in vastus lateralis muscle in 14 male type 2 diabetic patients (age 49.8 +/-2.1 years; BMI 27.2 +/-1.2 kg/m(2); mean +/- SE) with 16 male control subjects (age 48.0 +/-1.9 years; BMI 23.4 +/-0.6 kg/m(2)). We found that UCP3 protein levels were twice as low in patients with type 2 diabetes compared with control subjects (117 +/- 16 vs. 58 +/- 12 AU; P=0.007). There was no correlation between UCP3 content and BMI. In conclusion, UCP3 content is lower in type 2 diabetic patients compared with healthy control subjects. These results are consistent with a role for UCP3 in glucose homeostasis and suggest a role for UCP3 in type 2 diabetes.
引用
收藏
页码:2870 / 2873
页数:4
相关论文
共 20 条
[11]   MUSCLE-FIBER COMPOSITION AND CAPILLARY DENSITY IN WOMEN AND MEN WITH NIDDM [J].
MARIN, P ;
KROTKIEWSKI, M ;
ANDERSSON, B ;
BJORNTORP, P .
DIABETES CARE, 1994, 17 (05) :382-386
[12]   An uncoupling protein 3 gene polymorphism associated with a lower risk of developing Type II diabetes and with atherogenic lipid profile in a French cohort [J].
Meirhaeghe, A ;
Amouyel, P ;
Helbecque, N ;
Cottel, D ;
Otabe, S ;
Froguel, P ;
Vasseur, F .
DIABETOLOGIA, 2000, 43 (11) :1424-1428
[13]   UCP3 gene expression does not correlate with muscle oxidation rates in troglitazone-treated Zucker fatty rats [J].
Oberkofler, H ;
Neschen, S ;
Esterbauer, H ;
Waldhäusl, W ;
Patsch, W ;
Fürnsinn, C .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 2000, 1517 (01) :113-118
[14]   A novel polymorphism in the proximal UCP3 promoter region: effect on skeletal muscle UCP3 mRNA expression and obesity in male nondiabetic Pima Indians [J].
Schrauwen, P ;
Xia, J ;
Walder, K ;
Snitker, S ;
Ravussin, E .
INTERNATIONAL JOURNAL OF OBESITY, 1999, 23 (12) :1242-1245
[15]   The effect of weight reduction on skeletal muscle UCP2 and UCP3 mRNA expression and UCP3 protein content in Type II diabetic subjects [J].
Schrauwen, P ;
Schaart, G ;
Saris, WHM ;
Slieker, LJ ;
Glatz, JFC ;
Vidal, H ;
Blaak, EE .
DIABETOLOGIA, 2000, 43 (11) :1408-1416
[16]   Human uncoupling proteins and obesity [J].
Schrauwen, P ;
Walder, K ;
Ravussin, E .
OBESITY RESEARCH, 1999, 7 (01) :97-105
[17]   An alternative function for human uncoupling protein 3: protection of mitochondria against accumulation of nonesterified fatty acids inside the mitochondrial matrix [J].
Schrauwen, P ;
Saris, WHM ;
Hesselink, MKC .
FASEB JOURNAL, 2001, 15 (13) :2497-2502
[18]   Overexpression of GLUT4 in mice causes up-regulation of UCP3 mRNA in skeletal muscle [J].
Tsuboyama-Kasaoka, N ;
Tsunoda, N ;
Maruyama, K ;
Takahashi, M ;
Kim, H ;
Cooke, DW ;
Lane, MD ;
Ezaki, O .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 258 (01) :187-193
[19]   Up-regulation of uncoupling protein 3 (UCP3) mRNA by exercise training and down-regulation of UCP3 by denervation in skeletal muscles [J].
Tsuboyama-Kasaoka, N ;
Tsunoda, N ;
Maruyama, K ;
Takahashi, M ;
Kim, H ;
Ikemoto, S ;
Ezaki, O .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 247 (02) :498-503
[20]   Lack of skeletal muscle uncoupling protein 2 and 3 mRNA induction during fasting in type-2 diabetic subjects [J].
Vidal, H ;
Langin, D ;
Andreelli, F ;
Millet, L ;
Larrouy, D ;
Laville, M .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1999, 277 (05) :E830-E837