Metabolic Research Unit, School of Medicine, Deakin University, Waurn Ponds, 3217 Victoria, Australia.
Prostaglandins Leukot Essent Fatty Acids. 2011 Sep-Oct;85(3-4):155-61. doi: 10.1016/j.plefa.2011.06.002. Epub 2011 Jul 31.
Previous studies have shown that Eicosapentaenoic Acid (EPA) and Docosahexaenoic Acid (DHA) exhibit triacylglycerol (TAG) lowering effect in vitro and in vivo by down-regulating the Sterol Regulating Element Binding Protein (SREBP-1c) and reducing the expression levels of lipogenic genes. However, there is no evidence on the effect of Docosapentaenoic Acid (DPA) on SREBP-1c expression levels. DPA is a long chain n-3 fatty acid present in our diet through fish, red meat and milk of ruminant animals. Therefore, this study aimed to elucidate the effect of DPA on liver fatty acid synthesis in an in vitro model using rat liver cells. Our results suggested that DPA incubation (50μM) for 48h (like EPA and DHA) caused a significant decrease in the mRNA expression levels of SREBP-1c, 3-Hydroxy-3-Methyl-Glutaryl-Coenzyme A reductase (HMG-CoA reductase), Acetyl Coenzyme A Carboxylase (ACC-1) and Fatty Acid Synthase (FASn) compared with Oleic Acid (OA) and also a decrease in the protein levels of SREBP-1 and ACC-1. A time-course fatty acid analysis showed that DPA and EPA are interconvertable in the cells; however, after 8h of incubation with DPA, the cell phospholipids contained mainly DPA. The gene expression profiling of the lipogenic genes repeated at 8h confirmed that the inhibitory effect of DPA on mRNA expression levels of the lipogenic genes was most likely due to DPA itself and not due to its conversion into EPA.
先前的研究表明,二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)通过下调固醇调节元件结合蛋白(SREBP-1c)和降低脂肪生成基因的表达水平,在体外和体内显示出甘油三酯(TAG)降低的作用。然而,没有关于二十二碳五烯酸(DPA)对 SREBP-1c 表达水平影响的证据。DPA 是一种长链 n-3 脂肪酸,通过鱼类、红肉和反刍动物的牛奶存在于我们的饮食中。因此,本研究旨在使用大鼠肝细胞的体外模型阐明 DPA 对肝脏脂肪酸合成的影响。我们的结果表明,DPA 孵育(50μM)48h(与 EPA 和 DHA 一样)导致 SREBP-1c、3-羟-3-甲基戊二酰辅酶 A 还原酶(HMG-CoA 还原酶)、乙酰辅酶 A 羧化酶(ACC-1)和脂肪酸合酶(FASn)的 mRNA 表达水平显著降低,与油酸(OA)相比,SREBP-1 和 ACC-1 的蛋白水平也降低。脂肪酸分析表明,DPA 和 EPA 可在细胞内相互转化;然而,在用 DPA 孵育 8h 后,细胞磷脂主要含有 DPA。8h 时重复的脂肪生成基因表达谱分析证实,DPA 对脂肪生成基因 mRNA 表达水平的抑制作用很可能是由于 DPA 本身,而不是由于其转化为 EPA。