Department of Food and Nutritional Sciences, Ewha Womans University, Daehyun-Dong 11-1, Sudaemun-Gu, Seoul, 120-750, Republic of Korea.
Genes Nutr. 2008 Feb;2(4):327-30. doi: 10.1007/s12263-007-0068-8.
In this study, we investigated the lipolytic effects of eicosapentaenoic acid (EPA) in 3T3-L1 adipocytes. The differentiated 3T3-L1 adipocytes were treated in a serum-free medium with 300 muM of EPA for 3, 6, 12, and 24 h. In comparison with the control, intracellular lipid accumulation was significantly decreased by 24% at 24 h following the addition of EPA (P < 0.05). Under the same experimental conditions, there was an increase of glycerol and free fatty acids (FFAs). The mRNA level of carnitine palmitoyltransferase I-a, a component of the fatty-acid shuttle system involved in the mitochondrial oxidation of long-chain fatty acids, was also significantly elevated by EPA (P < 0.05). However, the expression of peroxisome proliferator-activated receptor-gamma and acetyl-CoA carboxylase (ACC), which are involved in adipogenesis, was significantly down-regulated by EPA (P < 0.05). These results suggest that EPA may modulate lipid metabolism by stimulation of lipolysis, which was associated with induction of lipolytic gene expression and suppression of adipogenic gene expression in 3T3-L1 adipocytes.
在这项研究中,我们研究了二十碳五烯酸(EPA)在 3T3-L1 脂肪细胞中的脂肪分解作用。将分化的 3T3-L1 脂肪细胞在无血清培养基中用 300 μM 的 EPA 处理 3、6、12 和 24 h。与对照组相比,添加 EPA 24 h 后细胞内脂质积累显著减少了 24%(P < 0.05)。在相同的实验条件下,甘油和游离脂肪酸(FFAs)增加。涉及长链脂肪酸线粒体氧化的脂肪酸穿梭系统的组成部分肉毒碱棕榈酰转移酶 I-a 的 mRNA 水平也被 EPA 显著上调(P < 0.05)。然而,参与脂肪生成的过氧化物酶体增殖物激活受体-γ和乙酰辅酶 A 羧化酶(ACC)的表达被 EPA 显著下调(P < 0.05)。这些结果表明,EPA 可能通过刺激脂肪分解来调节脂肪代谢,这与 3T3-L1 脂肪细胞中脂肪分解基因表达的诱导和脂肪生成基因表达的抑制有关。