DOI QR코드

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Oxidative stress and NRF2 signaling in kidney injury

  • Cherry Ng (Department of Pharmacy and BK21FOUR Advanced Program for Smart Pharma Leaders, Graduate School of The Catholic University of Korea) ;
  • Maxine Kim (Department of Pharmacy and BK21FOUR Advanced Program for Smart Pharma Leaders, Graduate School of The Catholic University of Korea) ;
  • Yanti (Faculty of Biotechnology, Atma Jaya Catholic University of Indonesia) ;
  • Mi‑Kyoung Kwak (Department of Pharmacy and BK21FOUR Advanced Program for Smart Pharma Leaders, Graduate School of The Catholic University of Korea)
  • 투고 : 2024.09.10
  • 심사 : 2024.11.30
  • 발행 : 2025.03.15

초록

Oxidative stress plays a crucial role in the pathogenesis of acute kidney injury (AKI), chronic kidney disease (CKD), and the AKI-to-CKD transition. This review examines the intricate relationship between oxidative stress and kidney pathophysiology, emphasizing the potential therapeutic role of nuclear factor erythroid 2-related factor 2 (NRF2), a master regulator of cellular redox homeostasis. In diverse AKI and CKD models, diminished NRF2 activity exacerbates oxidative stress, whereas genetic and pharmacological NRF2 activation alleviates kidney damage induced by nephrotoxic agents, ischemia-reperfusion injury, fibrotic stimuli, and diabetic nephropathy. The renoprotective effects of NRF2 extend beyond antioxidant defense, encompassing its anti-inflammatory and anti-fibrotic properties. The significance of NRF2 in renal fibrosis is further underscored by its interaction with the transforming growth factor-β signaling cascade. Clinical trials using bardoxolone methyl, a potent NRF2 activator, have yielded both encouraging and challenging outcomes, illustrating the intricacy of modulating NRF2 in human subjects. In summary, this overview suggests the therapeutic potential of targeting NRF2 in kidney disorders and highlights the necessity for continued research to refine treatment approaches.

키워드

과제정보

This study was supported by the National Research Foundation of Korea (NRF) grants funded by the Korean government [MSIT; grant numbers 2022R1A2C2011866 and 2018R1A6A1A03025108]. This study was also supported by the Research Fund, 2023 of The Catholic University of Korea.

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