Amentoflavone maintaining extracellular matrix homeostasis and inhibiting subchondral bone loss in osteoarthritis by inhibiting ERK, JNK and NF-κB signaling pathways

• Published in: Journal of orthopaedic surgery and research 2024-10, Vol.19 (1)
• Main Authors: Liang, Jianhui, Hu, Jiawei, Hong, Xin, Zhou, Ming, Xia, Guoming, Hu, Liangshen, Luo, Song, Quan, Kun, Yan, Jianbin, Wang, Song, Fan, Shaoyong
• Format: Article
• Language: English
• Subjects: Analysis; Bioflavonoids; Bone resorption; Care and treatment; Cellular signal transduction; Enzyme-linked immunosorbent assay; Ethylenediaminetetraacetic acid; Extracellular matrix; Flavones; Flavonoids; Genes; Health aspects; Inflammation; Muscle proteins; Osteoarthritis; Pharmacology, Experimental; Phosphatases; Physiological aspects; Protein kinases; RNA; Transcription factors
• ISSN: 1749-799X; 1749-799X
• DOI: 10.1186/s13018-024-05075-2

Amentoflavone (AF), a plant biflavone isolated from Selaginella sinensis ethanol extract, is characterized by anti-inflammatory and anti-oxidant properties. According to previous studies, inflammation and oxidative stress are closely related to the pathophysiology of osteoarthritis (OA). However, the effects and mechanisms of AF on OA have not been elucidated.To investigate the inhibitory effects and its molecular mechanism of AF on extracellular matrix (ECM) degradation stimulated by IL-1[beta] as well as subchondral bone loss induced by RANKL in mice chondrocytes. Quantitative PCR was used to detect the mRNA expression of genes related to inflammation, ECM, and osteoclast differentiation. Protein expression level of iNOS, COX-2, MMP13, ADAMTS5, COL2A1, SOX9, NFATc1, c-fos, JNK, ERK, P65, IκB[alpha] was measured by western blotting. The levels of TNF-[alpha] and IL-6 in the supernatants were measured by ELISA. The amount of ECM in chondrocytes was measured using toluidine blue staining. The levels of Aggrecan and Col2a1 in chondrocytes were measured using immunofluorescence. Tartrate-resistant acid phosphatase (TRAP) staining, F-actin staining and immunofluorescence were used to detect the effect of AF on osteoclast differentiation and bone resorption. The effect of AF on destabilization of the medial meniscus (DMM)-induced OA mice can be detected in hematoxylin-eosin (H&E) staining, Safranin O green staining and immunohistochemistry.AF might drastically attenuated IL-1[beta]-stimulated inflammation and reduction of ECM formation by blocking ERK and NF-κB signaling pathways in chondrocytes. Meanwhile, AF suppressed the formation of osteoclasts and the resorption of bone function induced by RANKL. In vivo, AF played a protective role by stabilizing cartilage ECM and inhibiting subchondral bone loss in destabilization of the medial meniscus (DMM)-induced OA mice, further proving its protective effect in the development of OA. Our study show that AF alleviated OA by suppressing ERK, JNK and NF-κB signaling pathways in OA models in vitro and DMM-induced OA mice, suggesting that AF might be a potential therapeutic agent in the treatment of OA. Keywords: Amentoflavone, Osteoarthritis, Extracellular matrix, Subchondral bone, Signaling pathway