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比沙库隆通过抑制脂肪生成和促进脂肪分解来抑制肝脏脂质积累。

Bisacurone suppresses hepatic lipid accumulation through inhibiting lipogenesis and promoting lipolysis.

作者信息

Ashida Hitoshi, Tian Xiaokuo, Kitakaze Tomoya, Yamashita Yoko

机构信息

Department of Agrobioscience, Graduate School of Agricultural Science, Kobe University, 1-1, Rokkodai-cho, Nada-ku, Kobe 657-8501, Japan.

出版信息

J Clin Biochem Nutr. 2020 Jul;67(1):43-52. doi: 10.3164/jcbn.20-16. Epub 2020 May 8.

Abstract

Turmeric and its components have various health beneficial functions. However, little is known about function of bisacurone, which is one of the sesquiterpenes in turmeric, at the compound level. In this study, we investigated the preventive effect of bisacurone on hepatic lipid accumulation and its mechanism in HepG2 cells and ICR mice. In HepG2 cells, bisacurone significantly inhibited fatty acid-induced intracellular lipid accumulation in a dose-dependent manner. Bisacurone at 10 µM increased protein expression of peroxisome proliferator-activated receptor α and carnitine palmitoyltransferase-1A accompanied by phosphorylation of AMP-activated protein kinase. In the liver of ICR mice, bisacurone decreased total lipids, triglyceride, and cholesterol contents. Bisacurone at 10 mg/kg body weight increased phosphorylation of AMP-activated protein kinase, and its downstream acetyl-CoA carboxylase as a rate-limiting enzyme for lipogenesis, while it decreased the nuclear translocation level of sterol regulatory element-binding protein 1 and carbohydrate-responsive element-binding protein as the major transcription factors for lipogenesis. On the other hand, bisacurone promoted lipolysis by up-expression of peroxisome proliferator-activated receptor α and carnitine palmitoyltransferase-1A. Thus, bisacurone might be a valuable food factor for preventing hepatic lipid accumulation by inhibiting lipogenesis and promoting lipolysis through phosphorylation of AMP-activated protein kinase.

摘要

姜黄及其成分具有多种有益健康的功能。然而,对于姜黄中的倍半萜之一双阿魏酸酮在化合物层面的功能却知之甚少。在本研究中,我们调查了双阿魏酸酮对HepG2细胞和ICR小鼠肝脏脂质积累的预防作用及其机制。在HepG2细胞中,双阿魏酸酮以剂量依赖性方式显著抑制脂肪酸诱导的细胞内脂质积累。10 μM的双阿魏酸酮增加了过氧化物酶体增殖物激活受体α和肉碱棕榈酰转移酶-1A的蛋白表达,并伴有AMP激活的蛋白激酶的磷酸化。在ICR小鼠的肝脏中,双阿魏酸酮降低了总脂质、甘油三酯和胆固醇含量。10 mg/kg体重的双阿魏酸酮增加了AMP激活的蛋白激酶及其下游作为脂肪生成限速酶的乙酰辅酶A羧化酶的磷酸化,同时降低了作为脂肪生成主要转录因子的固醇调节元件结合蛋白1和碳水化合物反应元件结合蛋白的核转位水平。另一方面,双阿魏酸酮通过过氧化物酶体增殖物激活受体α和肉碱棕榈酰转移酶-1A的上调表达促进脂肪分解。因此,双阿魏酸酮可能是一种有价值的食物因子,通过抑制脂肪生成和通过AMP激活的蛋白激酶的磷酸化促进脂肪分解来预防肝脏脂质积累。

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