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Bixin Attenuates Experimental Autoimmune Encephalomyelitis by Suppressing TXNIP/NLRP3 Inflammasome Activity and Activating NRF2 Signaling.
- Source :
-
Frontiers in immunology [Front Immunol] 2020 Dec 09; Vol. 11, pp. 593368. Date of Electronic Publication: 2020 Dec 09 (Print Publication: 2020). - Publication Year :
- 2020
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Abstract
- Multiple sclerosis (MS), an autoimmune and degenerative disease, is characterized by demyelination and chronic neuroinflammation. Bixin is a carotenoid isolated from the seeds of Bixa orellana that exhibits various potent pharmacological activities, including antioxidant, anti-inflammatory, and anti-tumor properties. However, the effects of bixin on MS have not yet been examined. To evaluate the effects and underlying molecular mechanisms of bixin on MS, experimental autoimmune encephalomyelitis (EAE) was established in C57BL/6 mice, which were treated via intragastric administration of bixin solutions. To evaluate the molecular mechanisms of bixin, quantitative reverse-transcription PCR, western blot, immunohistochemistry, flow cytometry, and enzyme-linked immunosorbent assay analyses were performed. We found that bixin significantly improved the symptoms and pathology in EAE mice, reduced the release of inflammatory cytokines TNF-α, IL-6, IL-8, IL-17, and IFN-γ, and increased the expression of the anti-inflammatory cytokine IL-10. And bixin reduced the proportion of Th1 and Th17 cells in the spleen and CNS, and suppressed microglia aggregation, and TXNIP/NLRP3 inflammasome activity by scavenging excessive reactive oxygen species (ROS) in EAE mice. Furthermore, bixin inhibited inflammation and oxidative stress via activating nuclear factor erythroid 2-related factor 2 (NRF2), and its downstream genes in EAE mice, meanwhile, these effects were suppressed upon treatment with an NRF2 inhibitor, ML385. Bixin prevented neuroinflammation and demyelination in EAE mice primarily by scavenging ROS through activation of the NRF2 signaling pathway. Taken together, our results indicate that bixin is a promising therapeutic candidate for treatment of MS.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2020 Yu, Wu, Li, Deng, Liu, Zhang, He, Zhao and Xu.)
- Subjects :
- Animals
Carotenoids chemistry
Cytokines metabolism
Demyelinating Diseases drug therapy
Demyelinating Diseases etiology
Demyelinating Diseases metabolism
Demyelinating Diseases pathology
Disease Models, Animal
Disease Susceptibility
Encephalomyelitis, Autoimmune, Experimental drug therapy
Encephalomyelitis, Autoimmune, Experimental pathology
Female
Lymphocyte Count
Mice
Oxidative Stress drug effects
Reactive Oxygen Species metabolism
T-Lymphocyte Subsets drug effects
T-Lymphocyte Subsets immunology
T-Lymphocyte Subsets metabolism
Carotenoids pharmacology
Carrier Proteins metabolism
Encephalomyelitis, Autoimmune, Experimental etiology
Encephalomyelitis, Autoimmune, Experimental metabolism
Inflammasomes metabolism
NF-E2-Related Factor 2 metabolism
NLR Family, Pyrin Domain-Containing 3 Protein metabolism
Signal Transduction drug effects
Thioredoxins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1664-3224
- Volume :
- 11
- Database :
- MEDLINE
- Journal :
- Frontiers in immunology
- Publication Type :
- Academic Journal
- Accession number :
- 33362775
- Full Text :
- https://doi.org/10.3389/fimmu.2020.593368