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Resveratrol reduces ROS-induced ferroptosis by activating SIRT3 and compensating the GSH/GPX4 pathway.

Xingjie WangTianli ShenJie LianKai DengChao QuEnmeng LiGan LiYiwei RenZijun WangZhengdong JiangXuejun SunXuqi Li
Published in: Molecular medicine (Cambridge, Mass.) (2023)
To date, this is the first study to show that resveratrol ameliorates intestinal ischemia-reperfusion injury by activating SIRT3 and reducing ferroptosis. Resveratrol can reduce intestinal ischemia-reperfusion injury by activating the SIRT3/FoxO3a pathway, increasing the expression of SOD2 and catalase, reducing ROS and LPO production, compensating for the GSH/GPX4 pathway and inhibiting ferroptosis. Resveratrol increases the expression of SOD2 and catalase, reduces the production of ROS and LPO, compensates for the GSH/GPX4 pathway and inhibits ferroptosis by activating the SIRT3/FoxO3a pathway.
Keyphrases
  • cell death
  • signaling pathway
  • oxidative stress
  • dna damage
  • poor prognosis
  • ischemia reperfusion injury
  • transcription factor
  • pi k akt
  • fluorescent probe
  • mouse model
  • cell proliferation
  • diabetic rats