The natural (poly)phenols as modulators of microglia polarization via TLR4/NF-κB pathway exert anti-inflammatory activity in ischemic stroke
- PMID: 34863710
- DOI: 10.1016/j.ejphar.2021.174660
The natural (poly)phenols as modulators of microglia polarization via TLR4/NF-κB pathway exert anti-inflammatory activity in ischemic stroke
Abstract
Increasing evidences suggest that inflammation plays a key role in the pathogenesis of stroke, a devastating disease second only to cardiac ischemia as a cause of death worldwide. Microglia are the first non-neuronal cells on the scene during the innate immune response to acute ischemic stroke. Microglia respond to acute brain injury by activating and developing classic M1-like (pro-inflammatory) or alternative M2-like (anti-inflammatory) phenotypes. M1 microglia produce pro-inflammatory cytokines to exacerbate neural death, astrocyte apoptosis, and blood brain barrier (BBB) disruption, while M2 microglia play the opposite role. NF-κB, a central regulator of the inflammatory response, was responsible for microglia M1 and M2 polarization. NF-κB p65 and p50 form a heterodimer to initiate a pro-inflammatory cytokine response, which enhances M1 activation and impair M2 response of microglia. TLR4, expressed on the surface of microglia, plays an important role in activating NF-κB, ultimately causing the M1 response of microglia. Therefore, modulation of microglial phenotypes via TLR4/NF-κB signaling pathway may be a promising therapeutic approach for ischemic stroke. Dietary (poly)phenols are present in various foods, which have shown promising protective effects on ischemic stroke. In vivo studies strongly suggest that many (poly)phenols have a pronounced impact on ischemic stroke, as demonstrated by lower neuroinflammation. Thus, this review focuses on the anti-inflammatory properties of dietary (poly)phenols and discusses their effects on the polarization of microglia through modulating TLR4/NF-κB signaling pathway in the ischemic stroke.
Keywords: (Poly)phenols; Anti-inflammation; Microglia; NF-κB; TLR4.
Copyright © 2021 Elsevier B.V. All rights reserved.
Similar articles
-
Candesartan modulates microglia activation and polarization via NF-κB signaling pathway.Int J Immunopathol Pharmacol. 2020 Jan-Dec;34:2058738420974900. doi: 10.1177/2058738420974900. Int J Immunopathol Pharmacol. 2020. PMID: 33237822 Free PMC article.
-
Oxymatrine inhibits neuroinflammation byRegulating M1/M2 polarization in N9 microglia through the TLR4/NF-κB pathway.Int Immunopharmacol. 2021 Nov;100:108139. doi: 10.1016/j.intimp.2021.108139. Epub 2021 Sep 10. Int Immunopharmacol. 2021. PMID: 34517275
-
Analgecine regulates microglia polarization in ischemic stroke by inhibiting NF-κB through the TLR4 MyD88 pathway.Int Immunopharmacol. 2021 Oct;99:107930. doi: 10.1016/j.intimp.2021.107930. Epub 2021 Jul 3. Int Immunopharmacol. 2021. PMID: 34229178
-
Ciprofloxacin and levofloxacin attenuate microglia inflammatory response via TLR4/NF-kB pathway.J Neuroinflammation. 2019 Jul 18;16(1):148. doi: 10.1186/s12974-019-1538-9. J Neuroinflammation. 2019. PMID: 31319868 Free PMC article. Review.
-
The Roles of RhoA/ROCK/NF-κB Pathway in Microglia Polarization Following Ischemic Stroke.J Neuroimmune Pharmacol. 2024 May 16;19(1):19. doi: 10.1007/s11481-024-10118-w. J Neuroimmune Pharmacol. 2024. PMID: 38753217 Review.
Cited by
-
4-methylumbilliferon (4-MU) as a Potential Treatment Against Cerebral ischemia and Reperfusion Injury in Rats; An Experimental Study.Arch Acad Emerg Med. 2024 Sep 17;13(1):e8. doi: 10.22037/aaem.v13i1.2456. eCollection 2025. Arch Acad Emerg Med. 2024. PMID: 39465056 Free PMC article.
-
Naotaifang III Protects Against Cerebral Ischemia Injury Through LPS/TLR4 Signaling Pathway in the Microbiota-Gut-Brain Axis.Drug Des Devel Ther. 2023 Dec 1;17:3571-3588. doi: 10.2147/DDDT.S421658. eCollection 2023. Drug Des Devel Ther. 2023. PMID: 38058793 Free PMC article.
-
Regulation of microglia polarization after cerebral ischemia.Front Cell Neurosci. 2023 Jun 8;17:1182621. doi: 10.3389/fncel.2023.1182621. eCollection 2023. Front Cell Neurosci. 2023. PMID: 37361996 Free PMC article. Review.
-
Design, synthesis, in vitro and in vivo biological evaluation of pterostilbene derivatives for anti-inflammation therapy.J Enzyme Inhib Med Chem. 2024 Dec;39(1):2315227. doi: 10.1080/14756366.2024.2315227. Epub 2024 Feb 29. J Enzyme Inhib Med Chem. 2024. PMID: 38421003 Free PMC article.
-
Exploring the Potential of Aptamers in Targeting Neuroinflammation and Neurodegenerative Disorders: Opportunities and Challenges.Int J Mol Sci. 2023 Jul 22;24(14):11780. doi: 10.3390/ijms241411780. Int J Mol Sci. 2023. PMID: 37511539 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials