The Nrf2 pathway in psychiatric disorders: pathophysiological role and potential targeting

被引:12
|
作者
Bhandari, Ranjana [1 ]
Kaur, Japneet [1 ]
Kaur, Simerpreet [1 ]
Kuhad, Anurag [1 ]
机构
[1] Panjab Univ, Pharmacol Res Lab, Univ Inst Pharmaceut Sci, UGC Ctr Adv Study, Chandigarh 160014, India
关键词
Nrf2-Keap1; oxidative Stress; psychiatric Disorders; antioxidants; neuroinflammation; reactive oxygen species (ROS); excitotoxicity; cytoprotective; OBSESSIVE-COMPULSIVE DISORDER; HEME OXYGENASE 1; NF-KAPPA-B; ANTIOXIDANT ENZYME-ACTIVITIES; ATTENUATES OXIDATIVE STRESS; NRF2/HO-1 SIGNALING PATHWAY; DEPRESSION-LIKE BEHAVIORS; AUTISM SPECTRUM DISORDER; DIMETHYL FUMARATE; ACTIVATES NRF2;
D O I
10.1080/14728222.2021.1887141
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: All psychiatric disorders exhibit excitotoxicity, mitochondrial dysfunction, inflammation, oxidative stress, and neural damage as their common characteristic. The endogenous nuclear factor erythroid 2-related factor 2 (Nrf2) signaling pathway is implicated in the defense mechanism against oxidative stress and has a significant role in psychiatric disorders. Areas covered: We explore the role of Nrf2 pathway and its modulators in psychiatric disorders. The literature was searched utilizing various databases such as Embase, Medline, Web of Science, Pub-Med, and Google Scholar from 2010 to 2020. The search included research articles, clinical reports, systematic reviews, and meta-analyses. Expert opinion: Environmental factors and genetic predisposition can be a trigger for the development of psychiatric disorders. Nrf2 downregulates certain inflammatory pathways and upregulates various antioxidant enzymes to maintain a balance. However, its intricate balance with NF-K beta (Nuclear factor kappa light chain enhancer of activated B cells) and its crosstalk with the transcription factor Nrf2 is critical in severe oxidative stress. Several Nrf2 modulators are now in clinical trials and can help reduce oxidative stress and neuroinflammation. There are immense potential opportunities for these modulators to become a novel therapeutic option.
引用
收藏
页码:115 / 139
页数:25
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