Recent advances in the study of Nrf2 and inflammatory respiratory diseases.
- Author:
Jian-lin XIE
;
Ming-bao LIN
;
Qi HOU
- Publication Type:Journal Article
- MeSH:
Acute Lung Injury;
metabolism;
pathology;
Antioxidants;
metabolism;
Glutathione;
Glutathione Transferase;
metabolism;
Humans;
Inflammation;
metabolism;
pathology;
Lung;
pathology;
NF-E2-Related Factor 2;
metabolism;
Oxidative Stress;
Pulmonary Disease, Chronic Obstructive;
metabolism;
pathology;
Signal Transduction
- From:
Acta Pharmaceutica Sinica
2015;50(9):1080-1087
- CountryChina
- Language:Chinese
-
Abstract:
Nuclear factor-erythroid 2 related factor 2 (Nrf2) is an ubiquitous and important transcription factor. It regulates antioxidant response elements (AREs)-mediated expression of antioxidant enzyme and cytoprotective proteins. A large body of research showed that Nrf2-Keap1 (Kelch-like ECH-associated protein 1, Keap 1)-ARE signaling pathway is involved in the endogenous antioxidant defense mechanisms. Nrf2 increases the expression of a number of cytoprotective genes, protects cells and tissues from the injury of a variety of toxicants and carcinogens. As a result, Nrf2 enhances the expression of glutathione and antioxidants such as superoxide dismutase and glutathione S-transferase, and subsequently scavenging free radicals. Air pollution especially from PM2.5 particles, is associated with an increasing morbidity of inflammatory pulmonary diseases and their deterioration. More and more studies demonstrated that Nrf2 was a novel signaling molecule in the modulation of inflammatory responses in these inflammatory respiratory diseases, such as asthma, acute lung injury (ALI) and COPD. Therefore, Nrf2 targeting might be a therapeutic target, which will provide clinical benefit by reducing both oxidative stress and inflammation in asthma, acute lung injury (ALI) and COPD. This review focused on the relationship between Nrf2 and inflammatory respiratory diseases and oxidative stress.
