1. The retinoid X receptor α modulator K-80003 suppresses inflammatory and catabolic responses in a rat model of osteoarthritis.
- Author
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Li H, Li X, Yang B, Su J, Cai S, Huang J, Hu T, Chen L, Xu Y, and Li Y
- Subjects
- Animals, Cartilage diagnostic imaging, Cartilage pathology, Cells, Cultured, Chondrocytes drug effects, Chondrocytes pathology, Disease Models, Animal, Estrogen Receptor alpha metabolism, HEK293 Cells, Humans, Inflammation diagnostic imaging, Joints drug effects, Joints pathology, Male, NF-kappa B metabolism, Osteoarthritis diagnostic imaging, Pain complications, Protective Agents pharmacology, Protein Binding drug effects, Rats, Sprague-Dawley, Signal Transduction drug effects, Sulindac pharmacology, Synovial Membrane drug effects, Synovial Membrane pathology, Synovitis complications, Synovitis pathology, Up-Regulation, Rats, Inflammation complications, Inflammation metabolism, Osteoarthritis complications, Osteoarthritis metabolism, Retinoid X Receptor alpha metabolism, Sulindac analogs & derivatives
- Abstract
Osteoarthritis (OA), a most common and highly prevalent joint disease, is closely associated with dysregulated expression and modification of RXRα. However, the role of RXRα in the pathophysiology of OA remains unknown. The present study aimed to investigate whether RXRα modulator, such as K-80003 can treat OA. Experimental OA was induced by intra-articular injection of monosodium iodoacetate (MIA) in the knee joint of rats. Articular cartilage degeneration was assessed using Safranin-O and fast green staining. Synovial inflammation was measured using hematoxylin and eosin (H&E) staining and enzyme-linked immunosorbent assay (ELISA). Expressions of MMP-13, ADAMTS-4 and ERα in joints were analyzed by immunofluorescence staining. Western blot, RT-PCR and co-Immunoprecipitation (co-IP) were used to assess the effects of K-80003 on RXRα-ERα interaction. Retinoid X receptor α (RXRα) modulator K-80003 prevented the degeneration of articular cartilage, reduced synovial inflammation, and alleviated osteoarthritic pain in rats. Furthermore, K-80003 markedly inhibited IL-1β-induced p65 nuclear translocation and IκBα degradation, and down-regulate the expression of HIF-2α, proteinases (MMP9, MMP13, ADAMTS-4) and pro-inflammatory factors (IL-6 and TNFα) in primary chondrocytes. Additionally, knockdown of ERα with siRNA blocked these effects of K-80003 in chondrocytes. In conclusion, RXRα modulators K-80003 suppresses inflammatory and catabolic responses in OA, suggesting that targeting RXRα-ERα interaction by RXRα modulators might be a novel therapeutic approach for OA treatment., (© 2021. The Author(s).)
- Published
- 2021
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