岩藻黄质
脂肪肝
生物
化学
生物化学
内科学
医学
疾病
类胡萝卜素
作者
Shouxing Yang,Jinhai Li,Liping Yan,Yu Wu,Lin Zhang,Boyang Li,Haibin Tong,Xiaochun Lin
标识
DOI:10.1021/acs.jafc.4c00590
摘要
mice. This modulation was accompanied by the activation of AMPK. The capacity of fucoxanthin to improve hepatic lipid deposition was significantly attenuated when utilizing the AMPK inhibitor or siRNA-mediated AMPK silencing. Mechanistically, fucoxanthin activates AMPK, subsequently regulating the KEAP1/Nrf2/ARE signaling pathway to exert antioxidative effects and stimulating the PGC1α/NRF1 axis to enhance mitochondrial biogenesis. These collective actions contribute to fucoxanthin's amelioration of hepatic steatosis induced by metabolic perturbations. These findings offer valuable insights into the prospective utilization of fucoxanthin as a therapeutic strategy for managing MAFLD.
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