Wang Yun, Torres-Gonzalez Moises, Tripathy Sasmita, Botolin Daniela, Christian Barbara, Jump Donald B
Department of Physiology, Michigan State University, East Lansing, MI 48824, USA.
J Lipid Res. 2008 Jul;49(7):1538-52. doi: 10.1194/jlr.M800123-JLR200. Epub 2008 Mar 30.
Hepatic fatty acid elongase-5 (Elovl-5) plays an important role in long chain monounsaturated and polyunsaturated fatty acid synthesis. Elovl-5 activity is regulated during development, by diet, hormones, and drugs, and in chronic disease. This report examines the impact of elevated Elovl-5 activity on hepatic function. Adenovirus-mediated induction of Elovl5 activity in livers of C57BL/6 mice increased hepatic and plasma levels of dihomo-gamma-linolenic acid (20:3,n-6) while suppressing hepatic arachidonic acid (20:4,n-6) and docosahexaenoic acid (22:6,n-3) content. The fasting-refeeding response of peroxisome proliferator-activated receptor alpha-regulated genes was attenuated in mice with elevated Elovl5 activity. In contrast, the fasting-refeeding response of hepatic sterol-regulatory element binding protein-1 (SREBP-1)-regulated and carbohydrate-regulatory element binding protein/Max-like factor X-regulated genes, Akt and glycogen synthase kinase (Gsk)-3beta phosphorylation, and the accumulation of hepatic glycogen content and nuclear SREBP-1 were not impaired by elevated Elovl5 activity. Hepatic triglyceride content and the phosphorylation of AMP-activated kinase alpha and Jun kinase 1/2 were reduced by elevated Elovl5 activity. Hepatic phosphoenolpyruvate carboxykinase expression was suppressed, while hepatic glycogen content and phosphorylated Gsk-3beta were significantly increased, in livers of fasted mice with increased Elovl5 activity. As such, hepatic Elovl5 activity may affect hepatic glucose production during fasting. In summary, Elovl5-induced changes in hepatic fatty acid content affect multiple pathways regulating hepatic lipid and carbohydrate composition.
肝脏脂肪酸延长酶-5(Elovl-5)在长链单不饱和脂肪酸和多不饱和脂肪酸合成中发挥重要作用。Elovl-5的活性在发育过程中、受饮食、激素、药物以及在慢性疾病中受到调控。本报告研究了Elovl-5活性升高对肝功能的影响。腺病毒介导的C57BL/6小鼠肝脏中Elovl5活性的诱导增加了肝脏和血浆中二十二碳三烯酸(20:3,n-6)的水平,同时抑制了肝脏中花生四烯酸(20:4,n-6)和二十二碳六烯酸(22:6,n-3)的含量。在Elovl5活性升高的小鼠中,过氧化物酶体增殖物激活受体α调控基因的禁食-再喂养反应减弱。相比之下,肝脏固醇调节元件结合蛋白-1(SREBP-1)调控和碳水化合物调节元件结合蛋白/Max样因子X调控基因的禁食-再喂养反应、Akt和糖原合酶激酶(Gsk)-3β磷酸化以及肝脏糖原含量和核SREBP-1的积累并未因Elovl5活性升高而受损。Elovl5活性升高降低了肝脏甘油三酯含量以及AMP激活的蛋白激酶α和Jun激酶1/2的磷酸化。在Elovl5活性增加的禁食小鼠肝脏中,肝脏磷酸烯醇式丙酮酸羧激酶表达受到抑制,而肝脏糖原含量和磷酸化Gsk-3β显著增加。因此,肝脏Elovl5活性可能影响禁食期间的肝脏葡萄糖生成。总之,Elovl5诱导的肝脏脂肪酸含量变化影响了调节肝脏脂质和碳水化合物组成的多个途径。