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首页> 外文期刊>BioMed research international >Crude Extracts fromLycium barbarumSuppress SREBP-1c Expression and Prevent Diet-Induced Fatty Liver through AMPK Activation
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Crude Extracts fromLycium barbarumSuppress SREBP-1c Expression and Prevent Diet-Induced Fatty Liver through AMPK Activation

机译:枸杞粗提物抑制SREBP-1c的表达并通过AMPK激活预防饮食诱导的脂肪肝

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Lycium barbarumpolysaccharide (LBP) is well known in traditional Chinese herbal medicine that, has beneficial effects. Previous study reported that LBP reduced blood glucose and serum lipids. However, the underlying LBP-regulating mechanisms remain largely unknown. The main purpose of this study was to investigate whether LBP prevented fatty liver through activation of adenosine monophosphate-activated protein kinase (AMPK) and suppression of sterol regulatory element-binding protein-1c (SREBP-1c). Male C57BL/6J mice were fed a low-fat diet, high-fat diet, or 100 mg/kg LBP-treatment diet for 24 weeks. HepG2 cells were treated with LBP in the presence of palmitic acid. In our study, LBP can improve body compositions and lipid metabolic profiles in high-fat diet-fed mice. Oil Red O stainingin vivoandin vitroshowed that LBP significantly reduced hepatic intracellular triacylglycerol accumulation. H&E staining also showed that LBP can attenuate liver steatosis. Hepatic genes expression profiles demonstrated that LBP can activate the phosphorylation of AMPK, suppress nuclear expression of SREBP-1c, and decrease protein and mRNA expression of lipogenic genesin vivoorin vitro. Moreover, LBP significantly elevated uncoupling protein-1 (UCP1) and peroxisome proliferator-activated receptor-γcoactivator-1α(PGC-1α) expression of brown adipose tissue. In summary, LBP possesses a potential novel treatment in preventing diet-induced fatty liver.
机译:枸杞多糖(LBP)在中草药中众所周知,具有有益的作用。先前的研究报道LBP可以降低血糖和血脂。但是,基本的LBP调节机制仍然未知。这项研究的主要目的是研究LBP是否通过激活腺苷一磷酸激活的蛋白激酶(AMPK)和抑制固醇调节元素结合蛋白1c(SREBP-1c)来预防脂肪肝。给雄性C57BL / 6J小鼠饲喂低脂饮食,高脂饮食或100μmg/ kg LBP治疗饮食24周。 HepG2细胞在棕榈酸存在下用LBP处理。在我们的研究中,LBP可以改善高脂饮食喂养小鼠的身体成分和脂质代谢状况。体内和体外油红O染色显示LBP显着降低了肝细胞内三酰甘油的积累。 H&E染色还显示LBP可减轻肝脏脂肪变性。肝基因表达谱表明,LBP在体内或体外均可激活AMPK的磷酸化,抑制SREBP-1c的核表达,并降低脂肪生成基因的蛋白质和mRNA表达。此外,LBP显着提高了棕色脂肪组织的解偶联蛋白-1(UCP1)和过氧化物酶体增殖物激活的受体-γcoactivator-1α(PGC-1α)的表达。总之,LBP在预防饮食引起的脂肪肝方面具有潜在的新疗法。

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