首页> 美国卫生研究院文献>Nutrients >Unripe Rubus coreanus Miquel Extract Containing Ellagic Acid Regulates AMPK SREBP-2 HMGCR and INSIG-1 Signaling and Cholesterol Metabolism In Vitro and In Vivo
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Unripe Rubus coreanus Miquel Extract Containing Ellagic Acid Regulates AMPK SREBP-2 HMGCR and INSIG-1 Signaling and Cholesterol Metabolism In Vitro and In Vivo

机译:含有鞣花酸的未成熟悬钩子提取物调节体内和体外AMPKSREBP-2HMGCR和INSIG-1信号传导及胆固醇代谢

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摘要

Our previous study demonstrated that a 5% ethanol extract of unripe (5- RCK) has hypo-cholesterolemic and anti-obesity activity. However, the molecular mechanisms of its effects are poorly characterized. We hypothesized that 5- RCK and one of its major bioactive compounds, ellagic acid, decrease cellular and plasma cholesterol levels. Thus, we investigated the hypocholesterolemic activity and mechanism of 5- RCK in both hepatocytes and a high-cholesterol diet (HCD)-induced rat model. Cholesterol in the liver and serum was significantly reduced by 5- RCK and ellagic acid. The hepatic activities of HMG-CoA and CETP were reduced, and the hepatic activity of LCAT was increased by both 5- RCK extract and ellagic acid, which also caused histological improvements. The MDA content in the aorta and serum was significantly decreased after oral administration of 5- RCK or ellagic acid. Further immunoblotting analysis showed that AMPK phosphorylation in the liver was induced by 5- RCK and ellagic acid, which activated AMPK, inhibiting the activity of HMGCR by inhibitory phosphorylation. In contrast, 5- RCK and ellagic acid suppressed the nuclear translocation and activation of SREBP-2, which is a key transcription factor in cholesterol biosynthesis. In conclusion, our results suggest that 5- RCK and its bioactive compound, ellagic acid, are useful alternative therapeutic agents to regulate blood cholesterol.
机译:我们以前的研究表明,未成熟的5%乙醇提取物(5- RCK)具有降胆固醇和抗肥胖的作用。但是,其作用的分子机制尚不明确。我们假设5-RCK及其主要生物活性化合物之一鞣花酸可降低细胞和血浆胆固醇水平。因此,我们调查了肝细胞和高胆固醇饮食(HCD)诱导的大鼠模型中5-RCK的降胆固醇活性和机制。 5-RCK和鞣花酸可显着降低肝脏和血清中的胆固醇。 5-RCK提取物和鞣花酸均降低了HMG-CoA和CETP的肝活性,并提高了LCAT的肝活性,这也导致组织学改善。口服5-RCK或鞣花酸后,主动脉和血清中的MDA含量显着降低。进一步的免疫印迹分析表明,肝脏中的AMPK磷酸化是由5-RCK和鞣花酸诱导的,鞣花酸激活AMPK,通过抑制性磷酸化抑制HMGCR的活性。相反,5-RCK和鞣花酸抑制了SREBP-2的核转运和活化,SREBP-2是胆固醇生物合成中的关键转录因子。总之,我们的结果表明5-RCK及其生物活性化合物鞣花酸是调节血液胆固醇的有用替代治疗剂。

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