Neschen Susanne, Morino Katsutaro, Dong Jianying, Wang-Fischer Yanlin, Cline Gary W, Romanelli Anthony J, Rossbacher Jörg C, Moore Irene K, Regittnig Werner, Munoz David S, Kim Jung H, Shulman Gerald I
Yale University School of Medicine, Howard Hughes Medical Institute, Departments of Internal Medicine, The Anlyan Center, P.O. Box 9812, New Haven, CT 06536-8012, USA.
Diabetes. 2007 Apr;56(4):1034-41. doi: 10.2337/db06-1206. Epub 2007 Jan 24.
Recent studies have suggested that n-3 fatty acids, abundant in fish oil, protect against high-fat diet-induced insulin resistance through peroxisome proliferator-activated receptor (PPAR)-alpha activation and a subsequent decrease in intracellular lipid abundance. To directly test this hypothesis, we fed PPAR-alpha null and wild-type mice for 2 weeks with isocaloric high-fat diets containing 27% fat from either safflower oil or safflower oil with an 8% fish oil replacement (fish oil diet). In both genotypes the safflower oil diet blunted insulin-mediated suppression of hepatic glucose production (P < 0.02 vs. genotype control) and PEPCK gene expression. Feeding wild-type mice a fish oil diet restored hepatic insulin sensitivity (hepatic glucose production [HGP], P < 0.002 vs. wild-type mice fed safflower oil), whereas in contrast, in PPAR-alpha null mice failed to counteract hepatic insulin resistance (HGP, P = NS vs. PPAR-alpha null safflower oil-fed mice). In PPAR-alpha null mice fed the fish oil diet, safflower oil plus fish oil, hepatic insulin resistance was dissociated from increases in hepatic triacylglycerol and acyl-CoA but accompanied by a more than threefold increase in hepatic diacylglycerol concentration (P < 0.0001 vs. genotype control). These data support the hypothesis that n-3 fatty acids protect from high-fat diet-induced hepatic insulin resistance in a PPAR-alpha-and diacylglycerol-dependent manner.
最近的研究表明,鱼油中富含的n-3脂肪酸通过激活过氧化物酶体增殖物激活受体(PPAR)-α以及随后降低细胞内脂质丰度来预防高脂饮食诱导的胰岛素抵抗。为了直接验证这一假设,我们用等热量的高脂饮食喂养PPAR-α基因敲除小鼠和野生型小鼠2周,这些高脂饮食含有27%来自红花油的脂肪,或者是用8%的鱼油替代红花油的饮食(鱼油饮食)。在两种基因型中,红花油饮食均减弱了胰岛素介导的对肝葡萄糖生成的抑制作用(与基因型对照相比,P < 0.02)以及磷酸烯醇式丙酮酸羧激酶(PEPCK)基因的表达。给野生型小鼠喂食鱼油饮食可恢复肝脏胰岛素敏感性(肝葡萄糖生成[HGP],与喂食红花油的野生型小鼠相比,P < 0.002),而相比之下,在PPAR-α基因敲除小鼠中未能抵消肝脏胰岛素抵抗(HGP,与喂食红花油的PPAR-α基因敲除小鼠相比,P = 无显著差异)。在喂食鱼油饮食、红花油加鱼油的PPAR-α基因敲除小鼠中,肝脏胰岛素抵抗与肝脏三酰甘油和酰基辅酶A的增加无关,但伴随着肝脏二酰甘油浓度增加超过三倍(与基因型对照相比,P < 0.ooo1)。这些数据支持了n-3脂肪酸以PPAR-α和二酰甘油依赖的方式预防高脂饮食诱导的肝脏胰岛素抵抗这一假设。