Nature Communications · 2019 · 75 citations · 43 references
PharmacyBiochemistryPharmacologyDrug DeliveryDrug DesignDrug DiscoveryLipid MetabolismLipid-based NanoparticlesLipid-lowering TherapyNanocarriers For TherapeuticsNanomedicineAortic Arch DiseaseAortic Arch InvolvementLipid-lowering Drug EfficacyLiver-specific Drug TargetingMedicinal Chemistry ApplicationsMetabolic Disease PharmacotherapyMicelle Drug DeliveryTherapeutic Targeting Of Metabolism
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.
43
2016 ESC/EAS Guidelines for the Management of Dyslipidaemias
Alberico L. Catapano, Ian Graham, Guy De Backer et al. · Atherosclerosis · 2016 · 1.6K citations · Full text