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Aged Oolong Tea Reduces High-Fat Diet-Induced Fat Accumulation and Dyslipidemia by Regulating the AMPK/ACC Signaling Pathway

机译:老化的乌龙茶可通过调节AMPK / ACC信号通路来减少高脂饮食诱导的脂肪积累和血脂异常

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摘要

While oolong tea (OT) has been shown to induce weight loss and reduce fat accumulation, the mechanisms remain poorly defined, especially for aged OT. In this study, five groups of mice (n = 9/group) were used including a normal diet with vehicle treatment, and a high-fat diet (HFD) with vehicle or the water extracts from aged OTs (EAOTs, three different storage years) by oral gavage at 1000 mg/kg·BW for 6 weeks. Body weight, fat accumulation, and serum biochemical parameters were used to evaluate obesity. The morphology of hepatocytes and adipocytes was analyzed by being stained with hematoxylin and eosin. The levels of p-AMPK, p-ACC (and non-phosphorylated versions), CPT-1 and FAS were determined by Western blotting and immunohistochemistry. EAOTs decreased HFD-induced body weight, fat accumulation, serum levels of triglyceride, total cholesterol, and low-density lipoprotein cholesterol, while enhancing the serum high-density lipoprotein cholesterol level. At the same time, EAOTs clearly alleviated fatty liver and reduced the size of adipocytes in the epididymal fat, especially in the 2006 group. Most importantly, EAOTs increased the phosphorylation of AMPK and ACC, and up-regulated the expression of CPT-1 but down-regulated the expression of fatty acid synthase, TNF-α and iNOS. Thus, EAOTs may inhibit obesity by up-regulating energy expenditure and fatty acid oxidation while inhibiting fatty acid synthesis and inflammation.
机译:虽然乌龙茶(OT)已被证明可引起体重减轻和减少脂肪堆积,但其机理仍知之甚少,特别是对于老年OT。在这项研究中,使用了五组小鼠(n = 9 /组),包括用媒介物处理的正常饮食和用媒介物或老年OTs(EAOTs)的水提取物进行的高脂饮食(HFD),三个不同的保存年限)以1000 mg / kg·BW的口管灌胃6周。体重,脂肪积累和血清生化参数用于评估肥胖。通过用苏木精和曙红染色来分析肝细胞和脂肪细胞的形态。通过蛋白质印迹和免疫组织化学测定p-AMPK,p-ACC(和非磷酸化版本),CPT-1和FAS的水平。 EAOTs降低了HFD诱导的体重,脂肪堆积,甘油三酸酯的血清水平,总胆固醇和低密度脂蛋白胆固醇,同时提高了血清高密度脂蛋白胆固醇水平。同时,EAOTs明显减轻了脂肪肝,减少了附睾脂肪中的脂肪细胞大小,特别是在2006年的人群中。最重要的是,EAOTs增加了AMPK和ACC的磷酸化,并上调了CPT-1的表达,但下调了脂肪酸合酶,TNF-α和iNOS的表达。因此,EAOTs可以通过上调能量消耗和脂肪酸氧化来抑制肥胖,同时抑制脂肪酸合成和炎症。

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