The possible role of nuclear factor erythroid-2-related factor 2 activators in the management of Covid-19.
Hayder M Al-KuraishyAli I Al-GareebOmayma A EldahshanYasmine M AbdelkhalekMagdy El DahshanEman A AhmedJean-Marc SabatierGaber E-S BatihaPublished in: Journal of biochemical and molecular toxicology (2023)
COVID-19 is caused by a novel SARS-CoV-2 leading to pulmonary and extra-pulmonary manifestations due to oxidative stress (OS) development and hyperinflammation. COVID-19 is primarily asymptomatic though it may cause acute lung injury (ALI), acute respiratory distress syndrome (ARDS), systemic inflammation, and thrombotic events in severe cases. SARS-CoV-2-induced OS triggers the activation of different signaling pathways, which counterbalances this complication. One of these pathways is nuclear factor erythroid 2-related factor 2 (Nrf2), which induces a series of cellular interactions to mitigate SARS-CoV-2-mediated viral toxicity and OS-induced cellular injury. Nrf2 pathway inhibits the expression of pro-inflammatory cytokines and the development of cytokine storm in COVID-19. Therefore, Nrf2 activators may play an essential role in reducing SARS-CoV-2 infection-induced inflammation by suppressing NLRP3 inflammasome in COVID-19. Furthermore, Nrf2 activators can attenuate endothelial dysfunction (ED), renin-angiotensin system (RAS) dysregulation, immune thrombosis, and coagulopathy. Thus this mini-review tries to clarify the possible role of the Nrf2 activators in the management of COVID-19. Nrf2 activators could be an effective therapeutic strategy in the management of Covid-19. Preclinical and clinical studies are recommended in this regard.
Keyphrases
- sars cov
- oxidative stress
- respiratory syndrome coronavirus
- diabetic rats
- coronavirus disease
- nuclear factor
- acute respiratory distress syndrome
- extracorporeal membrane oxygenation
- toll like receptor
- dna damage
- emergency department
- nlrp inflammasome
- induced apoptosis
- ischemia reperfusion injury
- immune response
- early onset
- stem cells
- cell proliferation
- mesenchymal stem cells
- bone marrow
- long non coding rna
- heat stress