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Attenuation of obesity and insulin resistance by fish oil supplementation is associated with improved skeletal muscle mitochondrial function in mice fed a high-fat diet

机译:鱼油补充肥胖和胰岛素抵抗的衰减与喂养高脂饮食的小鼠的改善骨骼肌线粒体功能有关

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Omega-3 polyunsaturated fatty acids (n-3 PUFAs) have been reported to improve insulin sensitivity and glucose homeostasis in animal models of insulin resistance, but the involved mechanisms still remain unresolved. In this study, we evaluated the effects of fish oil (FO), a source of n-3 PUFAs, on obesity, insulin resistance and muscle mitochondrial function in mice fed a high-fat diet (HFD). C57B1/6 male mice, 8 weeks old, were divided into four groups: control diet (C), high-fat diet (H), C+FO (CFO) and H+FO (HFO). FO was administered by oral gavage (2 g/kg b.w.), three times a week, starting 4 weeks before diet administration until the end of the experimental protocol. HFD-induced obesity and insulin resistance associated with impaired skeletal muscle mitochondrial function, as indicated by decreased oxygen consumption, tricarboxylic acid cycle intermediate (TCAi) contents (citrate, alpha-ketoglutarate, malate and oxaloacetate), oxidative phosphorylation protein content and mitochondrial biogenesis. These effects were associated with elevated reactive oxygen species production, decreased PGC1-a transcription and reduced Akt phosphorylation. The changes induced by the HFD were partially attenuated by FO, which decreased obesity and insulin resistance and increased mitochondria] function. In the H group, FO supplementation also improved oxygen consumption; increased TCAi content, and Akt and AMPK phosphorylation; and up-regulated mRNA expression of Gpat1, Pepck, catalase and mitochondrial proteins (Pgc1 alpha, Ppar alpha, Cpt1 and Ucp3). These results suggest that dietary FO attenuates the deleterious effects of the HFD (obesity and insulin resistance) by improving skeletal muscle mitochondrial function. (C) 2017 Elsevier Inc. All rights reserved.
机译:据报道,ω-3多不饱和脂肪酸(N-3 PUFA)以改善胰岛素抵抗的动物模型中的胰岛素敏感性和葡萄糖稳态,但涉及的机制仍然未解决。在这项研究中,我们评估了鱼油(FO),N-3 PUFA的源泉的影响,肥胖,喂养高脂饮食(HFD)的小鼠中的胰岛素抵抗和肌肉线粒体功能。 C57B1 / 6雄性小鼠,8周龄,分为四组:控制饮食(C),高脂饮食(H),C + FO(CFO)和H + FO(HFO)。通过口服饲养(2g / kg B.)给药,每周三次给药,在饮食给药前4周开始,直至实验方案结束。 HFD诱导的肥胖和胰岛素抵抗与骨骼肌线粒体功能有损的损伤相关,如氧气消耗量下降,三羧酸周期中间体(TCAI)含量(柠檬酸盐,α-酮戊酸盐,苹果酸盐和草酸),氧化磷酸化蛋白质含量和线粒体生物发生。这些效应与升高的反应性氧物质生产相关,降低PGC1-A转录和降低的AKT磷酸化。 HFD诱导的变化由FO部分衰减,这降低了肥胖症和胰岛素抵抗和增加的线粒体功能。在H组中,FO补充还改善了氧气消耗;增加TCAI内容,AKT和AMPK磷酸化; GPAT1,PEPCK,过氧化氢酶和线粒体蛋白(PGC1α,PPARα,CPT1和UCP3)的上调mRNA表达。这些结果表明,饮食通过改善骨骼肌线粒体功能来衰减HFD(肥胖和胰岛素抵抗)的有害影响。 (c)2017年Elsevier Inc.保留所有权利。

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