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首页> 外文期刊>The American journal of Chinese medicine >Epigallocatechin-3-Gallate-Rich Green Tea Extract Ameliorates Fatty Liver and Weight Gain in Mice Fed a High Fat Diet by Activating the Sirtuin 1 and AMP Activating Protein Kinase Pathway
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Epigallocatechin-3-Gallate-Rich Green Tea Extract Ameliorates Fatty Liver and Weight Gain in Mice Fed a High Fat Diet by Activating the Sirtuin 1 and AMP Activating Protein Kinase Pathway

机译:EpigallocateChin-3-gallate的绿茶提取物改善脂肪肝和小鼠的体重增加通过激活Sirtuin 1和AMP活化蛋白激酶途径通过激活高脂肪饮食

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摘要

The prevalence of metabolic diseases has risen globally in parallel with the obesity epidemic over the past few decades. Green tea has been reported to have metabolically beneficial effects on obesity; however, the mechanism by which green tea regulates lipid metabolism is not clearly understood. Male c57BL/6 mice were fed a normal chow diet, a high-fat diet (HFD), or an HFD supplemented with various doses of epigallocatechin gallate-rich green tea extract (GTE) for 12 weeks. GTE supplementation reduced body weight gain, prevented hepatic fat accumulation, decreased hypertriglyceridemia, and improved hyperglycemia and insulin resistance in HFD-fed mice. The underlying mechanisms of these beneficial effects of GTE might involve the upregulation of sirtuin 1 and AMP activated protein kinase (AMPK) and the downregulation of enzymes related to de novo lipogenesis. Consistent with the in vivo findings, GTE increased the expression and activity of sirtuin 1, enhanced the binding of sirtuin 1 to liver kinase B1 (LKB1) and subsequent deacetylation of LKB1, and reduced triglyceride accumulation in HepG2 cells. These results suggest the possible therapeutic potential of dietary epigallocatechin gallate-rich GTE supplementation for preventing the development and progression of hepatic steatosis and obesity.
机译:在过去的几十年里,代谢疾病的患病率与肥胖流行性平行上升。据报道,绿茶对肥胖具有代谢的有益影响;然而,绿茶调节脂质代谢的机制也没有清楚地理解。将雄性C57BL / 6小鼠喂养正常的食物饮食,高脂饮食(HFD)或补充有各种剂量的EPigallocateChin的HFD,富含富含剂量的绿茶提取物(GTE),12周。 GTE补充减少体重增加,预防肝脂肪积累,降低高甘油血症,以及改善HFD喂食小鼠的高血糖和胰岛素抵抗力。 GTE的这些有益效果的潜在机制可能涉及SIRTUIN 1和AMP活化蛋白激酶(AMPK)的上调和与DE Novo脂肪生成相关的酶的下调。与体内发现一致,GTE增加了Sirtuin1的表达和活性,增强了Sirtuin 1的结合,并随后对Lκ1的脱乙酰化,并降低了HepG2细胞中的甘油三酯积累。这些结果表明膳食EPIGALLOCATECHIN Gallate的GTE的可能治疗潜力,用于预防肝脏脂肪变性和肥胖的开发和进展。

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