Department of Human Health and Nutritional Sciences, University of Guelph, Guelph, ON, Canada.
Department of Pathobiology, University of Guelph, Guelph, ON, Canada.
J Lipid Res. 2024 Oct;65(10):100642. doi: 10.1016/j.jlr.2024.100642. Epub 2024 Sep 19.
The production of the omega-3 long-chain polyunsaturated fatty acids (n-3 LCPUFA) eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) from alpha-linolenic acid (ALA) relies on the delta-6 desaturase (D6D) enzyme encoded by the Fads2 gene. While EPA and DHA reduce hepatic triacylglycerol (TAG) storage and regulate lipogenesis, the independent impact of ALA is less understood. To address this gap in knowledge, hepatic fatty acid metabolism was investigated in male wild-type (WT) and Fads2 knockout (KO) mice fed diets (16% kcal from fat) containing either lard (no n-3 LCPUFA), flaxseed oil (ALA-rich), or menhaden oil (EPA/DHA rich) for 21 weeks. Fat content and composition, as well as markers of lipogenesis, glyceroneogenesis, and TAG synthesis, were analyzed using histology, gas chromatography, and reverse transcription quantitative PCR (RT-qPCR). Mice fed the menhaden diet had significantly lower hepatic TAG compared to both lard- and flax-fed mice, concomitant with changes in n-3 and n-6 LCPUFA in both TAG and phospholipid (PL) fractions (all P < 0.05). Flax-fed WT mice had lower liver TAG content compared to their KO counterparts. Menhaden-fed mice had significantly lower expression of key lipogenic (Scd1, Srebp-1c, Fasn, Fads1, and Fads2), glyceroneogenic (Pck1), and TAG synthesis (Agpat3) genes compared to lard, with flax-fed mice showing some intermediate effects. Gene expression effects were independent of D6D activity, since no differences were detected between WT and KO mice fed the same diet. This study demonstrates that EPA/DHA and not ALA itself is critical for the prevention of hepatic steatosis.
ω-3 长链多不饱和脂肪酸(n-3 LCPUFA)二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)由α-亚麻酸(ALA)生成依赖于 Fads2 基因编码的δ-6 去饱和酶(D6D)。虽然 EPA 和 DHA 可以减少肝三酰基甘油(TAG)的储存并调节脂肪生成,但 ALA 的独立作用却知之甚少。为了填补这一知识空白,研究人员用含猪油(不含 n-3 LCPUFA)、亚麻籽油(富含 ALA)或鲱鱼油(富含 EPA/DHA)的饮食(16%的热量来自脂肪)分别喂养雄性野生型(WT)和 Fads2 敲除(KO)小鼠 21 周,以此来研究雄性野生型(WT)和 Fads2 敲除(KO)小鼠的肝脂肪酸代谢。通过组织学、气相色谱和反转录定量 PCR(RT-qPCR)分析脂肪含量和组成以及脂肪生成、甘油酮生成和 TAG 合成的标志物。与饲喂猪油和亚麻籽油的小鼠相比,饲喂鲱鱼油的小鼠肝 TAG 含量显著降低,同时 TAG 和磷脂(PL)组分中的 n-3 和 n-6 LCPUFA 也发生了变化(均 P<0.05)。与 KO 相比,饲喂亚麻籽油的 WT 小鼠肝 TAG 含量更低。与饲喂猪油的小鼠相比,饲喂鲱鱼油的小鼠关键的脂肪生成基因(Scd1、Srebp-1c、Fasn、Fads1 和 Fads2)、甘油酮生成基因(Pck1)和 TAG 合成基因(Agpat3)的表达显著降低,而饲喂亚麻籽油的小鼠表现出一些中间效应。基因表达的影响与 D6D 活性无关,因为饲喂相同饮食的 WT 和 KO 之间没有差异。这项研究表明,EPA/DHA 而不是 ALA 本身对于预防肝脂肪变性至关重要。