Improved glucose homeostasis in mice overexpressing human UCP3: a role for AMP-kinase?

被引:37
作者
Schrauwen, P
Hardie, DG
Roorda, B
Clapham, JC
Abuin, A
Thomason-Hughes, M
Green, K
Frederik, PM
Hesselink, M
机构
[1] Maastricht Univ, Dept Human Biol, NUTRIM, NL-6200 MD Maastricht, Netherlands
[2] Univ Dundee, Wellcome Trust Bioctr, Dundee, Scotland
[3] GlaxoSmithKline, Dept Vasc Biol, Harlow, Essex, England
[4] GlaxoSmithKline, Dept Comparat Genet, Harlow, Essex, England
[5] Maastricht Univ, EM Unit, NL-6200 MD Maastricht, Netherlands
[6] Maastricht Univ, Dept Movement Sci, NL-6200 MD Maastricht, Netherlands
基金
英国惠康基金;
关键词
AMP-activated protein kinase; glucose metabolism; UCP3; diabetes; energy metabolism;
D O I
10.1038/sj.ijo.0802629
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: An unexplained phenotype of mice overexpressing human UCP3 is their improved glucose homeostasis. Since overexpression of UCP3 might affect the energy charge of the cell, we investigated whether these mice have an increased AMP-activated protein kinase (AMPK) activity. Methods: Mitochondrial localisation of UCP3 was determined by immunoelectronmicroscopy and AMPK activity was measured in medial gastrocnemius of control mice and mice overexpressing human UCP3. Results: Mice overexpressing human UCP3 had 5.8 fold higher levels of UCP3 protein, for which mitochondrial localisation was confirmed by immunoelectronmicroscopy. The ATP/AMP ratio was significantly lower in mice over-expressing UCP3 compared to the wild-type (10.9+/-1.6 vs 20.4+/-1.9 AU, P=0.03). Over-expression of UCP3 resulted in increased AMPK alpha1 activity (1.23+/-0.05 vs 1.00+/-0.06 normalized values, P=0.004) and a tendency towards increased AMPK alpha2 activity (1.18+/-0.08 vs 1.00+/-0.10 normalized values, P=0.08). Conclusion: Increased AMPK activity provides a plausible explanation for the improved glucose tolerance characteristic for these mice.
引用
收藏
页码:824 / 828
页数:5
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