小檗碱
体内
药理学
胶束
效力
聚乙二醇
肝病
医学
生物化学
化学
生物
体外
生物技术
物理化学
水溶液
作者
Huihui Guo,Chen‐Lin Feng,Wenxuan Zhang,Zhigang Luo,Hongjuan Zhang,Tingting Zhang,Chen Ma,Yun Zhan,Rui Li,Song Wu,Zeper Abliz,Cong Li,Xiaolin Li,Xiaolei Ma,Lu‐Lu Wang,Wensheng Zheng,Yanxing Han,Jian‐Dong Jiang
标识
DOI:10.1038/s41467-019-09852-0
摘要
Abstract Cardiovascular and metabolic disease (CMD) remains a main cause of premature death worldwide. Berberine (BBR), a lipid-lowering botanic compound with diversified potency against metabolic disorders, is a promising candidate for ameliorating CMD. The liver is the target of BBR so that liver-site accumulation could be important for fulfilling its therapeutic effect. In this study a rational designed micelle (CTA-Mic) consisting of α-tocopheryl hydrophobic core and on-site detachable polyethylene glycol-thiol shell is developed for effective liver deposition of BBR. The bio-distribution analysis proves that the accumulation of BBR in liver is increased by 248.8% assisted by micelles. Up-regulation of a range of energy-related genes is detectable in the HepG2 cells and in vivo. In the high fat diet-fed mice, BBR-CTA-Mic intervention remarkably improves metabolic profiles and reduces the formation of aortic arch plaque. Our results provide proof-of-concept for a liver-targeting strategy to ameliorate CMD using natural medicines facilitated by Nano-technology.
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