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Targeting STATs in neuroinflammation: The road less traveled!
- Source :
-
Pharmacological research [Pharmacol Res] 2019 Mar; Vol. 141, pp. 73-84. Date of Electronic Publication: 2018 Dec 11. - Publication Year :
- 2019
-
Abstract
- JAK/STAT transduction pathway is a highly conserved pathway implicated in regulating cellular proliferation, differentiation, survival and apoptosis. Dysregulation of this pathway is involved in the onset of autoimmune, haematological, oncological, metabolic and neurological diseases. Over the last few years, the research of anti-neuroinflammatory agents has gained considerable attention. The ability to diminish the STAT-induced transcription of inflammatory genes is documented for both natural compounds (such as polyphenols) and chemical drugs. Among polyphenols, quercetin and curcumin directly inhibit STAT, while Berberis vulgaris L. and Sophora alopecuroides L extracts act indirectly. Also, the Food and Drug Administration has approved several JAK/STAT inhibitors (direct or indirect) for treating inflammatory diseases, indicating STAT can be considered as a therapeutic target for neuroinflammatory pathologies. Considering the encouraging data obtained so far, clinical trials are warranted to demonstrate the effectiveness and potential use in the clinical practice of STAT inhibitors to treat inflammation-associated neurodegenerative pathologies.<br /> (Copyright © 2018 Elsevier Ltd. All rights reserved.)
- Subjects :
- Animals
Anti-Inflammatory Agents pharmacology
Humans
Inflammation metabolism
Nervous System Diseases metabolism
Polyphenols pharmacology
Polyphenols therapeutic use
STAT Transcription Factors chemistry
STAT Transcription Factors metabolism
Anti-Inflammatory Agents therapeutic use
Inflammation drug therapy
Nervous System Diseases drug therapy
STAT Transcription Factors antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 1096-1186
- Volume :
- 141
- Database :
- MEDLINE
- Journal :
- Pharmacological research
- Publication Type :
- Academic Journal
- Accession number :
- 30550953
- Full Text :
- https://doi.org/10.1016/j.phrs.2018.12.004