Protective Effects of an Oligo-Fucoidan-Based Formula against Osteoarthritis Development via iNOS and COX-2 Suppression following Monosodium Iodoacetate Injection.
Yi-Fen ChiangKo-Chieh HuangKai-Lee WangYun-Ju HuangHsin-Yuan ChenMohamed AliTzong-Ming ShiehShih Min HsiaPublished in: Marine drugs (2024)
Osteoarthritis (OA) is a debilitating joint disorder characterized by cartilage degradation and chronic inflammation, accompanied by high oxidative stress. In this study, we utilized the monosodium iodoacetate (MIA)-induced OA model to investigate the efficacy of oligo-fucoidan-based formula (FF) intervention in mitigating OA progression. Through its capacity to alleviate joint bearing function and inflammation, improvements in cartilage integrity following oligo-fucoidan-based formula intervention were observed, highlighting its protective effects against cartilage degeneration and structural damage. Furthermore, the oligo-fucoidan-based formula modulated the p38 signaling pathway, along with downregulating cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) expression, contributing to its beneficial effects. Our study provides valuable insights into targeted interventions for OA management and calls for further clinical investigations to validate these preclinical findings and to explore the translational potential of an oligo-fucoidan-based formula in human OA patients.
Keyphrases
- nitric oxide synthase
- oxidative stress
- knee osteoarthritis
- human milk
- nitric oxide
- diabetic rats
- signaling pathway
- randomized controlled trial
- rheumatoid arthritis
- endothelial cells
- induced apoptosis
- poor prognosis
- end stage renal disease
- ejection fraction
- dna damage
- extracellular matrix
- stem cells
- newly diagnosed
- cell proliferation
- epithelial mesenchymal transition
- mesenchymal stem cells
- drug induced
- pi k akt
- low birth weight
- ischemia reperfusion injury
- bone marrow
- human health
- heat shock