Low-Molecular-Weight Fish Collagen Peptide (Valine-Glycine-Proline-Hydroxyproline-Glycine-Proline-Alanine-Glycine) Prevents Osteoarthritis Symptoms in Chondrocytes and Monoiodoacetate-Injected Rats.
Wonhee ChoJeongjin ParkJinhee KimMinhee LeeSo Jung ParkKyung Seok KimWoojin JunOk-Kyung KimJeongmin LeePublished in: Marine drugs (2023)
The objective of this study was to investigate the effect of low-molecular-weight fish collagen (valine-glycine-proline-hydroxyproline-glycine-proline-alanine-glycine; LMWCP) on H 2 O 2 - or LPS-treated primary chondrocytes and monoiodoacetate (MIA)-induced osteoarthritis rat models. Our findings indicated that LMWCP treatment exhibited protective effects by preventing chondrocyte death and reducing matrix degradation in both H 2 O 2 -treated primary chondrocytes and cartilage tissue from MIA-induced osteoarthritis rats. This was achieved by increasing the levels of aggrecan, collagen type I, collagen type II, TIMP-1, and TIMP-3, while simultaneously decreasing catabolic factors such as phosphorylation of Smad, MMP-3, and MMP-13. Additionally, LMWCP treatment effectively suppressed the activation of inflammation and apoptosis pathways in both LPS-treated primary chondrocytes and cartilage tissue from MIA-induced osteoarthritis rats. These results suggest that LMWCP supplementation ameliorates the progression of osteoarthritis through its direct impact on inflammation and apoptosis in chondrocytes.
Keyphrases
- oxidative stress
- diabetic rats
- extracellular matrix
- rheumatoid arthritis
- high glucose
- knee osteoarthritis
- inflammatory response
- endoplasmic reticulum stress
- cell death
- mouse model
- wound healing
- endothelial cells
- cell cycle arrest
- epithelial mesenchymal transition
- depressive symptoms
- cell proliferation
- newly diagnosed
- combination therapy
- signaling pathway