» Articles » PMID: 36815898

Cerium Oxide Nanoparticles Protect Against Chondrocytes and Cartilage Explants from Oxidative Stress Nrf2/HO-1 Pathway in Temporomandibular Joint Osteoarthritis

Overview
Date 2023 Feb 23
PMID 36815898
Authors
Affiliations
Soon will be listed here.
Abstract

Oxidative stress is closely linked to the etiology of temporomandibular joint osteoarthritis. (TMJ-OA) and is an important therapeutic target. Cerium oxide nanoparticles (CNPs) have been broadly studied owing to their powerful antioxidant properties and potential preventive and therapeutic effects against chronic diseases. The current study was designed to explore the protective effects of CNPs on the progression of TMJ-OA and their potential mechanisms. We detected the ability of CNPs to eliminate reactive oxygen species (ROS) in chondrocytes. Moreover, their protective effects on chondrocytes were detected in the level of gene and protein. Furthermore, TUNEL assay, histology and safranin O-fast green staining were used to detect the beneficial effects of CNPs on cartilage explants. The mechanism of CNPs, protecting condylar cartilage by reducing inflammation, was further explored by knocking down the Nuclear factor-erythroid 2-related factor (Nrf2) gene. CNPs could reduce the ROS levels in chondrocytes and cartilage explants and reverse the IL-1β-induced imbalance of cartilage matrix metabolism and apoptosis. The protective effects of CNPs on cartilage were lost after key antioxidant factors including Nrf2 and heme-oxygenase 1(HO-1) were significantly reduced. In conclusion, this study demonstrated for the first time that activating the Nrf2/HO-1 signaling pathway by CNPs might have therapeutic potential for TMJ-OA.

Citing Articles

Effects of Cerium Oxide on Kidney and Liver Tissue Damage in an Experimental Myocardial Ischemia-Reperfusion Model of Distant Organ Damage.

Gunes I, Dursun A, Ozdemir C, Kucuk A, Sezen S, Arslan M Medicina (Kaunas). 2025; 60(12.

PMID: 39768923 PMC: 11728079. DOI: 10.3390/medicina60122044.


Edge advances in nanodrug therapies for osteoarthritis treatment.

Liao J, Gu Q, Liu Z, Wang H, Yang X, Yan R Front Pharmacol. 2024; 15:1402825.

PMID: 39539625 PMC: 11559267. DOI: 10.3389/fphar.2024.1402825.


Dual role of Nrf2 signaling in hepatocellular carcinoma: promoting development, immune evasion, and therapeutic challenges.

Gan L, Wang W, Jiang J, Tian K, Liu W, Cao Z Front Immunol. 2024; 15:1429836.

PMID: 39286246 PMC: 11402828. DOI: 10.3389/fimmu.2024.1429836.


The regulatory mechanisms of cerium oxide nanoparticles in oxidative stress and emerging applications in refractory wound care.

Yi L, Yu L, Chen S, Huang D, Yang C, Deng H Front Pharmacol. 2024; 15:1439960.

PMID: 39156103 PMC: 11327095. DOI: 10.3389/fphar.2024.1439960.


Poly(-coumaric acid) nanoparticles alleviate temporomandibular joint osteoarthritis by inhibiting chondrocyte ferroptosis.

Guo J, Su K, Wang L, Feng B, You X, Deng M Bioact Mater. 2024; 40:212-226.

PMID: 38973989 PMC: 11224931. DOI: 10.1016/j.bioactmat.2024.06.007.


References
1.
Serebrovska Z, Swanson R, Portnichenko V, Shysh A, Pavlovich S, Tumanovska L . Anti-inflammatory and antioxidant effect of cerium dioxide nanoparticles immobilized on the surface of silica nanoparticles in rat experimental pneumonia. Biomed Pharmacother. 2017; 92:69-77. DOI: 10.1016/j.biopha.2017.05.064. View

2.
Ren B, Kwah M, Liu C, Ma Z, Shanmugam M, Ding L . Resveratrol for cancer therapy: Challenges and future perspectives. Cancer Lett. 2021; 515:63-72. DOI: 10.1016/j.canlet.2021.05.001. View

3.
Bolduc J, Collins J, Loeser R . Reactive oxygen species, aging and articular cartilage homeostasis. Free Radic Biol Med. 2018; 132:73-82. PMC: 6342625. DOI: 10.1016/j.freeradbiomed.2018.08.038. View

4.
Gorrini C, Harris I, Mak T . Modulation of oxidative stress as an anticancer strategy. Nat Rev Drug Discov. 2013; 12(12):931-47. DOI: 10.1038/nrd4002. View

5.
Jiang C, Luo P, Li X, Liu P, Li Y, Xu J . Nrf2/ARE is a key pathway for curcumin-mediated protection of TMJ chondrocytes from oxidative stress and inflammation. Cell Stress Chaperones. 2020; 25(3):395-406. PMC: 7192998. DOI: 10.1007/s12192-020-01079-z. View