Jump D B, Clarke S D, Thelen A, Liimatta M
Department of Physiology, Michigan State University, East Lansing 48824.
J Lipid Res. 1994 Jun;35(6):1076-84.
Using a combination of in vivo and in vitro studies, we have investigated the impact of polyunsaturated fatty acids (PUFA) on the expression of several genes encoding proteins involved in hepatic glycolysis and lipogenesis. Meal-training rats to a high glucose diet containing 10% triolein led to a significant induction of hepatic mRNAs encoding glucokinase (GK), pyruvate kinase (PK), fatty acid synthase (FAS), malic enzyme (ME), and the S14 protein (S14), but had no effect on thyroid hormone receptor-beta 1 (TR beta 1) and c/EBP alpha gene expression. Replacing triolein with menhaden oil attenuated (by 50-90%) the induction of mRNA encoding GK, ME, PK, FAS, and S14. This effect was rapid (within hours) and for FAS and S14, directed at the transcriptional level. The mRNAs encoding TR beta 1, c/EBP alpha and beta-actin were unaffected by menhaden oil. Studies with cultured primary hepatocytes showed that C18:3,omega 3 (n-3), C18:3,omega 6 (n-6), C20:4, omega 6 (n-6), and C20:5,omega 3 (n-3) were all equally effective at suppressing the level of mRNAs encoding FAS, S14, and PK. This effect was specific for glycolytic and lipogenic enzymes, as expression of beta-actin was not affected by these fatty acids. Moreover, the fatty acids had only marginal effects on cell viability as judged by lactate dehydrogenase release. These data indicate that polyunsaturated fatty acids coordinately regulate the expression of several enzymes involved in carbohydrate and lipid metabolism. The mechanism of control does not require extrahepatic factors or fatty acid metabolism.
通过体内和体外研究相结合的方法,我们研究了多不饱和脂肪酸(PUFA)对几种参与肝脏糖酵解和脂肪生成的蛋白质编码基因表达的影响。让大鼠适应含10%三油精的高糖饮食,可显著诱导肝脏中编码葡萄糖激酶(GK)、丙酮酸激酶(PK)、脂肪酸合酶(FAS)、苹果酸酶(ME)和S14蛋白(S14)的mRNA表达,但对甲状腺激素受体β1(TRβ1)和c/EBPα基因表达没有影响。用鲱鱼油替代三油精可减弱(50 - 90%)编码GK、ME、PK、FAS和S14的mRNA的诱导表达。这种作用迅速(数小时内),对于FAS和S14而言,是在转录水平上起作用。编码TRβ1、c/EBPα和β-肌动蛋白的mRNA不受鲱鱼油影响。对原代培养肝细胞的研究表明,C18:3,ω3(n - 3)、C18:3,ω6(n - 6)、C20:4,ω6(n - 6)和C20:5,ω3(n - 3)在抑制编码FAS、S14和PK的mRNA水平方面同样有效。这种作用对糖酵解和脂肪生成酶具有特异性,因为β-肌动蛋白的表达不受这些脂肪酸影响。此外,通过乳酸脱氢酶释放判断,这些脂肪酸对细胞活力的影响很小。这些数据表明,多不饱和脂肪酸协同调节几种参与碳水化合物和脂质代谢的酶的表达。调控机制不需要肝外因子或脂肪酸代谢参与。