Schrauwen Patrick, Hoeks Joris, Hesselink Matthijs K C
Nutrition and Toxicology Research Institute Maastricht (NUTRIM), Department of Human Biology, Maastricht University, P.O. Box 616, 6200 MD, Maastricht, The Netherlands.
Prog Lipid Res. 2006 Jan;45(1):17-41. doi: 10.1016/j.plipres.2005.11.001. Epub 2005 Dec 9.
The discovery of the human homologue of the thermogenic protein UCP1, named uncoupling protein 3 (UCP3), boosted research on the role of this skeletal muscle protein in energy metabolism and body weight regulation. Nowadays, 9 years after its discovery emerging data indicate that the primary physiological role of UCP3 may be the mitochondrial handling of fatty acids rather than regulating energy expenditure via thermogenesis. UCP3 has been proposed to export fatty acid anions or fatty acid peroxides away from the matrix-side of the mitochondrial inner membrane to prevent their deleterious accumulation. In this way, UCP3 could protect mitochondria against lipid-induced oxidative mitochondrial damage, a function especially important under conditions of high fatty acid supply to skeletal muscle mitochondria. Such function may be clinically relevant in the development of type 2 diabetes mellitus, a condition characterized by muscular fat accumulation, mitochondrial damage and low levels of UCP3.
产热蛋白UCP1的人类同源物——解偶联蛋白3(UCP3)的发现,推动了关于这种骨骼肌蛋白在能量代谢和体重调节中作用的研究。如今,在其发现9年后,新出现的数据表明,UCP3的主要生理作用可能是线粒体对脂肪酸的处理,而非通过产热来调节能量消耗。有人提出,UCP3可将脂肪酸阴离子或脂肪酸过氧化物从线粒体内膜的基质侧输出,以防止它们有害地积累。通过这种方式,UCP3可以保护线粒体免受脂质诱导的氧化性线粒体损伤,这一功能在向骨骼肌线粒体大量供应脂肪酸的情况下尤为重要。这种功能在2型糖尿病的发展过程中可能具有临床相关性,2型糖尿病的特征是肌肉脂肪堆积、线粒体损伤和UCP3水平较低。