Abstract | BACKGROUND:
Glaucoma is the leading cause of irreversible blindness in the world. Elevated intraocular pressure (IOP) is recognized as one of the most critical factors, but the loss of retinal ganglia cells (RGCs) often persists when IOP is controlled. Recently, a large number of studies focus on the inflammatory and immune responses in the occurrence and development of glaucoma. Magnolol (MAG), the principal ingredient of magnoliae officinalis cortex, has anti-inflammatory effects, but its role and mechanism in retinal protection need to be further studied. METHODS: The neurodegeneration of retina in mice model following ischemia/reperfusion (IR) injury was evaluated by immunohistochemistry, hematoxylin and eosin (H&E) staining and electroretinography (ERG). The inflammation-regulatory effect of MAG was detected by quantitative RT-PCR, western blot, and immunohistochemistry. Peroxisome proliferator-activated receptor-γ (PPARγ) inhibitor assays by H&E staining and western blot were used to test the target and mechanism pathway of MAG. RESULTS: We found MAG relieved IR-induced retinal damages and inflammation. Further studies revealed MAG alleviated nuclear factor kappa B (NFκB)-dependent inflammatory process by preserving the expression of NFκB inhibitor alpha (IκBα), and it modulated microglia polarization after IR injury. PPARγ was a primary target of MAG, and treatment with PPARγ inhibitor GW9662 attenuated the neuroprotective and anti-inflammatory effects of MAG. CONCLUSIONS: Our findings revealed that MAG inhibits NFκB-dependent inflammatory processes by elevating PPARγ in mice retinas to achieve its neuroprotective role following IR, which suggesting that MAG could be developed to a novel anti-inflammatory therapeutic agent for relieving the progression of glaucoma.
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Authors | Ning Wang, Yijie Yang, Yixin Liu, Lulu Huang, Mengyang Gu, Yue Wu, Li Xu, Hao Sun, Wenyi Guo |
Journal | International immunopharmacology
(Int Immunopharmacol)
Vol. 112
Pg. 109242
(Nov 2022)
ISSN: 1878-1705 [Electronic] Netherlands |
PMID | 36152538
(Publication Type: Journal Article)
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Copyright | Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved. |
Chemical References |
- NF-kappa B
- PPAR gamma
- magnolol
- NF-KappaB Inhibitor alpha
- Eosine Yellowish-(YS)
- Hematoxylin
- Anti-Inflammatory Agents
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Topics |
- Animals
- Mice
- NF-kappa B
(metabolism)
- PPAR gamma
(metabolism)
- NF-KappaB Inhibitor alpha
(metabolism)
- Eosine Yellowish-(YS)
(metabolism, pharmacology, therapeutic use)
- Hematoxylin
(metabolism, pharmacology, therapeutic use)
- Reperfusion Injury
(drug therapy, metabolism)
- Retina
(metabolism)
- Inflammation
(drug therapy, metabolism)
- Glaucoma
- Disease Models, Animal
- Anti-Inflammatory Agents
(pharmacology, therapeutic use, metabolism)
- Ischemia
(metabolism)
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