Rajna Alex, Brown Liam Hayden, Frangos Sara Michaela, Gonzalez-Soto Melissa, Hucik Barbora, Wang Chenxuan, Wright David Charles, Mutch David Michael
Department of Human Health & Nutritional Sciences, University of Guelph, Guelph, Ontario, Canada.
Department of Human Health & Nutritional Sciences, University of Guelph, Guelph, Ontario, Canada.
J Nutr Biochem. 2022 Apr;102:108940. doi: 10.1016/j.jnutbio.2022.108940. Epub 2022 Jan 10.
Marine sourced N3-PUFA regulate lipid metabolism in adipose tissue and liver; however, less is known about plant sourced N3-PUFA. The goal of this study was to investigate plant and marine N3-PUFA regulation of fatty acid trafficking along the adipose tissue-liver axis according to nutritional state. Mice were fed low-fat diets (7% w/w) containing either lard, flaxseed, or menhaden oils for 8 weeks, and were euthanized in either fed or fasted states. Substrate utilization and physical activity were assessed during the transition from a fed to fasted state. Plasma biomarkers (triacylglycerol [TAG], non-esterified fatty acids [NEFA]), as well as liver and epididymal adipose tissue (eWAT) lipogenic and lipolytic markers, were measured. Neither plant nor marine N3-PUFA influenced substrate utilization or activity during the transition from a fed to fasted state. In the fed state, marine N3-PUFA reduced plasma TAG levels compared to the other diets, with no further reduction seen in fasted mice. Hepatic lipogenic markers (Fasn, Acc, Scd1, and Elovl6) were reduced in the fed state with marine N3-PUFA, but not plant N3-PUFA. In the fasted state, mice fed either N3-PUFA accumulated less liver TAG, had lower plasma NEFA, and suppressed eWAT HSL activity compared to lard. Marine N3-PUFA are more potent regulators of lipogenesis than plant N3-PUFA in the fed state, whereas both N3-PUFA influence eWAT lipolysis and plasma NEFA in the fasted state. This work provides novel insights regarding N3-PUFA regulation of fatty acid trafficking along the adipose tissue-liver axis according to nutritional state.
海洋来源的n-3多不饱和脂肪酸(N3-PUFA)可调节脂肪组织和肝脏中的脂质代谢;然而,对于植物来源的N3-PUFA了解较少。本研究的目的是根据营养状态,研究植物和海洋来源的N3-PUFA对沿脂肪组织-肝脏轴的脂肪酸转运的调节作用。给小鼠喂食含猪油、亚麻籽或鲱鱼油的低脂饮食(7% w/w)8周,并在喂食或禁食状态下实施安乐死。在从喂食状态转变为禁食状态的过程中评估底物利用和身体活动情况。测量血浆生物标志物(三酰甘油[TAG]、非酯化脂肪酸[NEFA])以及肝脏和附睾脂肪组织(eWAT)的脂肪生成和脂肪分解标志物。在从喂食状态转变为禁食状态的过程中,植物和海洋来源的N3-PUFA均未影响底物利用或活动情况。在喂食状态下,与其他饮食相比,海洋来源的N3-PUFA可降低血浆TAG水平,禁食小鼠中未见进一步降低。在喂食状态下,海洋来源的N3-PUFA可降低肝脏脂肪生成标志物(Fasn、Acc、Scd1和Elovl6),但植物来源的N3-PUFA则无此作用。在禁食状态下,与喂食猪油的小鼠相比,喂食任何一种N3-PUFA的小鼠肝脏TAG积累较少,血浆NEFA较低,且附睾脂肪组织HSL活性受到抑制。在喂食状态下,海洋来源的N3-PUFA比植物来源的N3-PUFA对脂肪生成的调节作用更强,而在禁食状态下,两种N3-PUFA均影响附睾脂肪组织的脂肪分解和血浆NEFA。这项工作为根据营养状态,N3-PUFA对沿脂肪组织-肝脏轴的脂肪酸转运的调节提供了新的见解。