Department of Pharmaceutical Sciences, University of Salerno, Fisciano, Italy.
J Cell Physiol. 2011 Jan;226(1):187-93. doi: 10.1002/jcp.22323.
We evaluated, in human cell line HepG2, the action of individual dietary polyunsaturated fatty acids (PUFAs) on the expression of several lipid metabolism genes. The effects of docosahexaenoic acid, 22:6, n-3 (DHA), eicosapentaenoic acid, 20:5, n-3 (EPA), and arachidonic acid, 20:4, n-6 (AA) were studied alone and with vitamin E (Vit.E). DHA, EPA, and AA down-regulated mRNAs and encoded proteins of stearoyl-CoA desaturase (SCD) and sterol regulatory element binding protein (SREBP-1c), two major factors involved in unsaturated fatty acids synthesis. DHA affected SREBP-1c mRNA less markedly than EPA and AA. Vit.E did not affect these products, both when individually added or together with fatty acids. The expression of UDP-glucuronosyl transferase 1A1 (UGT1A1) mRNA, an enzyme of phase II drug metabolism with relevant actions within lipid metabolism, resulted also differentially regulated. DHA did not essentially reduce UGT1A1 mRNA expression while EPA and AA produced a considerable decrease. Nevertheless, when these PUFAs were combined with Vit.E, which by itself did not produce any effect, the result was a reduction of UGT1A1 mRNA with DHA, an increase reverting to basal level with EPA and no variation with AA. Observed regulations did not result to be mediated by peroxisome proliferator-activated receptor (PPAR). Our data indicate that major dietary PUFAs and Vit.E are differentially and selectively able to affect the expression of genes involved in lipid metabolism. The different actions of these slightly different molecules could be associated with their physiological role as relevant nutrient molecules.
我们在 HepG2 人细胞系中评估了单一膳食多不饱和脂肪酸 (PUFA) 对几种脂质代谢基因表达的作用。研究了二十二碳六烯酸(DHA)、二十碳五烯酸(EPA)和花生四烯酸(AA)的作用,单独研究和与维生素 E(Vit.E)一起研究。DHA、EPA 和 AA 下调了硬脂酰辅酶 A 去饱和酶 (SCD) 和固醇调节元件结合蛋白 (SREBP-1c) 的 mRNA 和编码蛋白,这两种因子在不饱和脂肪酸合成中起主要作用。DHA 对 SREBP-1c mRNA 的影响不如 EPA 和 AA 明显。Vit.E 不影响这些产物,无论是单独添加还是与脂肪酸一起添加。UDP-葡萄糖醛酸转移酶 1A1 (UGT1A1) mRNA 的表达也受到不同的调节,UGT1A1 mRNA 是一种与脂质代谢相关的药物代谢相 II 期的酶。DHA 并未显著降低 UGT1A1 mRNA 的表达,而 EPA 和 AA 则产生了相当大的降低。然而,当这些 PUFAs 与 Vit.E 结合时,Vit.E 本身不会产生任何影响,结果是 DHA 降低了 UGT1A1 mRNA,EPA 则使 UGT1A1 mRNA 恢复到基础水平,AA 则没有变化。观察到的调节并非由过氧化物酶体增殖物激活受体 (PPAR) 介导。我们的数据表明,主要的膳食 PUFAs 和 Vit.E 能够以不同的方式选择性地影响参与脂质代谢的基因的表达。这些略有不同的分子的不同作用可能与其作为相关营养分子的生理作用有关。