Protective Effects of an Oligo-Fucoidan-Based Formula against Osteoarthritis Development via iNOS and COX-2 Suppression following Monosodium Iodoacetate Injection

Author:

Chiang Yi-Fen1,Huang Ko-Chieh1,Wang Kai-Lee2,Huang Yun-Ju3,Chen Hsin-Yuan1ORCID,Ali Mohamed45ORCID,Shieh Tzong-Ming6ORCID,Hsia Shih-Min178910ORCID

Affiliation:

1. School of Nutrition and Health Sciences, College of Nutrition, Taipei Medical University, Taipei 110301, Taiwan

2. Department of Nursing, Deh Yu College of Nursing and Health, Keelung 203301, Taiwan

3. Department of Biotechnology and Food Technology, Southern Taiwan University of Science and Technology, Tainan 710301, Taiwan

4. Department of Obstetrics and Gynecology, University of Chicago, Chicago, IL 60637, USA

5. Clinical Pharmacy Department, Faculty of Pharmacy, Ain Shams University, Cairo 11566, Egypt

6. School of Dentistry, China Medical University, Taichung 404328, Taiwan

7. Graduate Institute of Metabolism and Obesity Sciences, College of Nutrition, Taipei Medical University, Taipei 11031, Taiwan

8. School of Food and Safety, Taipei Medical University, Taipei 11031, Taiwan

9. Nutrition Research Center, Taipei Medical University Hospital, Taipei 11031, Taiwan

10. TMU Research Center for Digestive Medicine, Taipei Medical University, Taipei 11031, Taiwan

Abstract

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.

Publisher

MDPI AG

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