Forsythiaside A Activates AMP-Activated Protein Kinase and Regulates Oxidative Stress via Nrf2 Signaling

    Young Eun Kim, Seon-Been Bak, Min‐Jin Kim, Su-Jin Bae, Won-Yung Lee, Young Woo Kim
    Forsythiaside A (FA), derived from Forsythia suspensa, exhibits protective effects against oxidative stress by activating AMP-activated protein kinase (AMPK) and modulating the Nrf2 signaling pathway. In HepG2 cells, FA reduces apoptosis and mitochondrial dysfunction caused by arachidonic acid and iron, enhancing cell viability and decreasing reactive oxygen species (ROS) production. It also upregulates antioxidant enzymes through the ERK-AMPK-Nrf2 pathway. In vivo studies in mice show that FA reduces liver damage from carbon tetrachloride exposure, indicating its potential as an antioxidant therapeutic agent for liver protection.
    Discuss this study in the Community →

    Research cited in this study

    3 / 3 results

    Related Community Posts Join

    0 / 0 results
    — no results

    Similar Research

    5 / 27 results