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首页> 外文期刊>Physiological Reports >Fish oil reverses metabolic syndrome, adipocyte dysfunction, and altered adipokines secretion triggered by high‐fat diet‐induced obesity
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Fish oil reverses metabolic syndrome, adipocyte dysfunction, and altered adipokines secretion triggered by high‐fat diet‐induced obesity

机译:鱼油逆转代谢综合征,脂肪细胞功能障碍,并改变高脂饮食诱导肥胖引发的adipokines分泌物

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The effect of fish oil (FO) treatment on high‐fat (HF) diet‐induced obesity and metabolic syndrome was addressed by analyzing dysfunctions in cells of different adipose depots. For this purpose, mice were initially induced to obesity for 8?weeks following a treatment with FO containing high concentration of EPA compared to DHA (5:1), for additional 8?weeks (by gavage, 3 times per week). Despite the higher fat intake, the HF group showed lower food intake but higher body weight, glucose intolerance and insulin resistance, significant dyslipidemia and increased liver, subcutaneous (inguinal‐ING) and visceral (retroperitoneal‐RP) adipose depots mass, accompanied by adipocyte hypertrophy and decreased cellularity in both adipose tissue depots. FO treatment reversed all these effects, as well as it improved the metabolic activities of isolated adipocytes, such as glucose uptake and lipolysis in both depots, and de novo synthesis of fatty acids in ING adipocytes. HF diet also significantly increased both the pro and anti‐inflammatory cytokines expression by adipocytes, while HF?+?FO did not differ from control group. Collectively, these data show that the concomitant administration of FO with the HF diet is able to revert metabolic changes triggered by the diet‐induced obesity, as well as to promote beneficial alterations in adipose cell activities. The main mechanism underlying all systemic effects involves direct and differential effects on ING and RP adipocytes.
机译:通过分析不同脂肪贮库的细胞的功能障碍,通过分析了多脂肪(HF)饮食肥胖症和代谢综合征的鱼油(FO)处理的影响。为此目的,与DHA(5:1)相比,含有高浓度的EPA的治疗后,最初将小鼠肥胖为8?周,另外8?周(每周3次3次)。尽管脂肪摄入量较高,但HF组表现出较低的食物摄入量,但体重较高,葡萄糖不耐受,胰岛素,显着的血脂血症和肝脏增加,皮下(induinal-ing)和内脏(逆床(逆床型-RP)伴有脂肪细胞伴有脂肪细胞脂肪组织仓库中的肥大和细胞减少。 Fo治疗逆转了所有这些效果,以及它改善了孤立的脂肪细胞的代谢活动,例如葡萄糖摄取和脂肪分解,在脂肪细胞中的脂肪酸中的脂肪酸。 HF饮食也显着增加了脂肪细胞的亲和抗炎细胞因子表达,而HF?+ΔFO与对照组没有不同。总的来说,这些数据显示,随着HF饮食的伴随施用FO能够恢复由饮食诱导的肥胖症引发的代谢变化,以及促进脂肪细胞活性的有益改变。所有全身效应的主要机制涉及对ING和RP脂肪细胞的直接和差异效应。

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