Ribot Joan, Portillo Maria P, Picó Catalina, Macarulla M Teresa, Palou Andreu
Bioquímica, Biología Molecular, Nutrición y Biotecnología (Nutrigenómica), Universitat de les Illes Balears (UIB), Cra. Valldemossa, km 7.5, 07122 Palma de Mallorca, Spain.
Br J Nutr. 2007 Jun;97(6):1074-82. doi: 10.1017/S0007114507682932. Epub 2007 Mar 7.
It is known that conjugated linoleic acid (CLA) feeding decreases body adiposity but the mechanisms involved are not clear. The aim of this study was to analyse whether alterations in uncoupling protein (UCP) expression in white and brown adipose tissues (WAT and BAT, respectively) and in skeletal muscle may be responsible for the effect of trans-10, cis-12 CLA on the size of body fat depots in hamsters. Animals were divided into three groups and fed an atherogenic diet with different amounts of trans-10, cis-12 CLA (0 control, 0.5, or 1 g/100 g diet) for 6 weeks. CLA feeding reduced adipose depot weights, but had no effect on body weight. Leptin mRNA expression decreased in both subcutaneous and perirenal WAT depots, in accordance with lower adiposity, whereas resistin mRNA expression was not changed. Animals fed CLA had lower UCP1 mRNA levels in BAT (both doses of CLA) and in perirenal WAT (the low dose), and lower UCP3 mRNA levels in subcutaneous WAT (the high dose). UCP2 mRNA expression in WAT was not significantly affected by CLA feeding. Animals fed the high dose of CLA showed increased UCP3 and carnitine palmitoyl transferase-I (CPT-I) mRNA expression levels in skeletal muscle. In summary, induction of UCP1 or UCP2 in WAT and BAT is not likely to be responsible for the fat-reduction action of CLA, but the increased expression of UCP3 in skeletal muscle, together with a higher expression of CPT-I, may explain the previously reported effects of dietary CLA in lowering adiposity and increasing fatty acid oxidation by skeletal muscle.
已知喂食共轭亚油酸(CLA)可降低身体肥胖程度,但其涉及的机制尚不清楚。本研究的目的是分析白色和棕色脂肪组织(分别为WAT和BAT)以及骨骼肌中解偶联蛋白(UCP)表达的改变是否可能是反式10,顺式12 CLA对仓鼠体内脂肪库大小产生影响的原因。将动物分为三组,喂食含有不同量反式10,顺式12 CLA(0对照、0.5或1 g/100 g饮食)的致动脉粥样化饮食6周。喂食CLA可降低脂肪库重量,但对体重没有影响。瘦素mRNA表达在皮下和肾周WAT库中均降低,这与较低的肥胖程度一致,而抵抗素mRNA表达未改变。喂食CLA的动物BAT(两种CLA剂量)和肾周WAT(低剂量)中的UCP1 mRNA水平较低,皮下WAT(高剂量)中的UCP3 mRNA水平较低。CLA喂食对WAT中UCP2 mRNA表达没有显著影响。喂食高剂量CLA的动物骨骼肌中UCP3和肉碱棕榈酰转移酶-I(CPT-I)mRNA表达水平升高。总之,WAT和BAT中UCP1或UCP2的诱导不太可能是CLA减脂作用的原因,但骨骼肌中UCP3表达的增加以及CPT-I表达的升高,可能解释了先前报道的饮食CLA在降低肥胖和增加骨骼肌脂肪酸氧化方面的作用。