首页> 外文期刊>Journal of Agricultural and Food Chemistry >Sechium edule Shoot Extracts and Active Components Improve Obesity and a Fatty Liver That Involved Reducing Hepatic Lipogenesis and Adipogenesis in High-Fat-Diet-Fed Rats
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Sechium edule Shoot Extracts and Active Components Improve Obesity and a Fatty Liver That Involved Reducing Hepatic Lipogenesis and Adipogenesis in High-Fat-Diet-Fed Rats

机译:Sechium edule茎提取物和活性成分改善肥胖和高脂饮食喂养大鼠肝脏脂肪形成和脂肪形成的脂肪肝。

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Excess fat accumulation in the liver increases the risk of developing progressive liver injuries ranging from a fatty liver to hepatocarcinoma. In a previous study, we demonstrated that the polyphenol components of Sechium edule shoots attenuated hepatic lipid accumulation in vitro. Therefore, we investigated the effects and mechanisms of the extract of S. edule shoots (SINE) to modulate fat accumulation in a high-fat-diet (HFD)-induced animal model. In this study, we found that the SINE can reduce the body weight, adipose tissue fat, and regulate hepatic lipid contents (e.g., triglyceride and cholesterol). Additionally, treatment of Caffeic acid (CA) and hesperetin (HPT), the main ingredients of SINE, also inhibited oleic acid (OA)-induced lipid accumulation in HepG2 cells. SWE enhanced the activation of AMP-activating protein kinase (AMPK) and decreased numerous lipogenic-related enzymes, such as sterol regulator element-binding proteins (SREBPs), e.g., SREBP-1 and SREBP-2, and HMG-CoA reductase (HMGCoR) proteins, which are critical regulators of hepatic lipid metabolism. Taken together, The results demonstrated that SINE can prevent a fatty liver and attenuate adipose tissue fat by inhibiting lipogenic enzymes and stimulating lipolysis via upregulating AMPK. It was also demonstrated that the main activation components of EWE are both CA and HPT.
机译:肝脏中过多的脂肪积累会增加发生进行性肝损伤的风险,从脂肪肝到肝癌不等。在先前的研究中,我们证明了Sechium edule芽的多酚成分在体外可减轻肝脂质的积累。因此,我们调查了高脂饮食(HFD)诱导的动物模型中小枝茎茎提取物(SINE)调节脂肪积累的作用和机制。在这项研究中,我们发现SINE可以减轻体重,脂肪组织脂肪并调节肝脂质含量(例如甘油三酸酯和胆固醇)。此外,对SINE的主要成分咖啡酸(CA)和橙皮素(HPT)的治疗也抑制了油酸(OA)诱导的HepG2细胞脂质蓄积。 SWE增强了AMP激活蛋白激酶(AMPK)的激活并减少了许多与脂肪生成有关的酶,例如固醇调节因子结合蛋白(SREBPs),例如SREBP-1和SREBP-2,以及HMG-CoA还原酶(HMGCoR )蛋白,它们是肝脂质代谢的关键调节剂。两者合计,结果表明SINE可以通过抑制脂肪酶和通过上调AMPK刺激脂解作用来预防脂肪肝并减轻脂肪。还证明了EWE的主要激活成分是CA和HPT。

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