The effect of UCP3 overexpression on mitochondrial ROS production in skeletal muscle of young versus aged mice

被引:72
作者
Nabben, Miranda [1 ]
Hoeks, Joris [1 ]
Briede, Jacob J. [2 ,3 ]
Glatz, Jan F. C. [4 ]
Moonen-Kornips, Esther [1 ]
Hesselink, Matthijs K. C.
Schrauwen, Patrick [1 ]
机构
[1] Maastricht Univ, Dept Human Biol, NUTRIM, NL-6200 MD Maastricht, Netherlands
[2] Maastricht Univ, Dept Hlth Risk Anal, NUTRIM, NL-6200 MD Maastricht, Netherlands
[3] Maastricht Univ, Dept Toxicol, NUTRIM, NL-6200 MD Maastricht, Netherlands
[4] Maastricht Univ, Dept Mol Genet, Cardiovasc Res Inst Maastricht, NL-6200 MD Maastricht, Netherlands
关键词
UCP3; ROS; Aging; Mitochondria; 4-HNE; Mild uncoupling;
D O I
10.1016/j.febslet.2008.11.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Uncoupling protein 3 (UCP3) is suggested to protect mitochondria against aging and lipid-induced damage, possibly via modulation of reactive oxygen species (ROS) production. Here we show that mice overexpressing UCP3 (UCP3Tg) have a blunted age-induced increase in ROS production, assessed by electron spin resonance spectroscopy, but only after addition of 4-hydroxynonenal (4-HNE). Mitochondrial function, assessed by respirometry, on glycolytic substrate was lower in UCP3Tg mice compared to wild types, whereas this tended to be higher on fatty acids. State 4o respiration was higher in UCP3Tg animals. To conclude, UCP3 overexpression leads to increased state 4o respiration and, in presence of 4-HNE, blunts the age-induced increase in ROS production. (c) 2008 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:4147 / 4152
页数:6
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