Role of Peroxiredoxins in Protecting Against Cardiovascular and Related Disorders.
Y Robert LiHong ZhuIgor DanelisenPublished in: Cardiovascular toxicology (2021)
Peroxiredoxin (Prx) refers to a family of thiol-dependent peroxidases that decompose hydrogen peroxide, lipid hydroperoxides, as well as peroxynitrite, and protect against oxidative and inflammatory stress. There are six mammalian Prx isozymes (Prx1-6), classified as typical 2-Cys, atypical 2-Cys, or 1-Cys Prxs based on the mechanism and the number of cysteine residues involved during catalysis. In addition to their well-established peroxide-scavenging activity, some Prxs also participate in the regulation of various cell signaling pathways. Extensive animal studies employing primarily gene knockout models provide substantial evidence supporting a critical protective role of Prxs in various disease processes involving oxidative and inflammatory stress. This review surveys recent research findings, published primarily in influential journals, on the involvement of various Prx isozymes in protecting against cardiovascular injury and related disorders, including diabetes, metabolic syndromes, and sepsis, whose pathophysiology all intimately involves oxidative stress and inflammation.
Keyphrases
- oxidative stress
- hydrogen peroxide
- induced apoptosis
- nitric oxide
- dna damage
- type diabetes
- diabetic rats
- ischemia reperfusion injury
- signaling pathway
- living cells
- cardiovascular disease
- fluorescent probe
- single cell
- acute kidney injury
- intensive care unit
- cell therapy
- stress induced
- genome wide
- cross sectional
- systematic review
- septic shock
- epithelial mesenchymal transition
- case control
- fatty acid
- heat stress
- randomized controlled trial
- bone marrow
- metabolic syndrome
- single molecule
- genome wide identification
- insulin resistance