Nutraceutical Strategies for Suppressing NLRP3 Inflammasome Activation: Pertinence to the Management of COVID-19 and Beyond.
Mark F McCartySimon Bernard Iloki AssangaLidianys Lewis LujánJames H O'KeefeJames J Di NicolantonioPublished in: Nutrients (2020)
Inflammasomes are intracellular protein complexes that form in response to a variety of stress signals and that serve to catalyze the proteolytic conversion of pro-interleukin-1β and pro-interleukin-18 to active interleukin-1β and interleukin-18, central mediators of the inflammatory response; inflammasomes can also promote a type of cell death known as pyroptosis. The NLRP3 inflammasome has received the most study and plays an important pathogenic role in a vast range of pathologies associated with inflammation-including atherosclerosis, myocardial infarction, the complications of diabetes, neurological and autoimmune disorders, dry macular degeneration, gout, and the cytokine storm phase of COVID-19. A consideration of the molecular biology underlying inflammasome priming and activation enables the prediction that a range of nutraceuticals may have clinical potential for suppressing inflammasome activity-antioxidants including phycocyanobilin, phase 2 inducers, melatonin, and N-acetylcysteine, the AMPK activator berberine, glucosamine, zinc, and various nutraceuticals that support generation of hydrogen sulfide. Complex nutraceuticals or functional foods featuring a number of these agents may find utility in the prevention and control of a wide range of medical disorders.
Keyphrases
- nlrp inflammasome
- coronavirus disease
- cell death
- inflammatory response
- sars cov
- cardiovascular disease
- oxidative stress
- signaling pathway
- healthcare
- type diabetes
- anti inflammatory
- multiple sclerosis
- optical coherence tomography
- lipopolysaccharide induced
- reactive oxygen species
- left ventricular
- immune response
- binding protein
- risk assessment
- toll like receptor
- cell proliferation
- human health
- diabetic retinopathy
- lps induced
- insulin resistance
- single molecule
- protein kinase
- brain injury