AI Article Synopsis

  • Osteoarthritis (OA) is a common degenerative joint disease characterized by persistent inflammation, and this review investigates the anti-inflammatory effects of resveratrol as a potential treatment.
  • A systematic search for studies on resveratrol’s impact on animal models of OA identified 15 relevant studies, revealing that resveratrol reduces harmful inflammatory factors and restores joint structure.
  • The findings suggest that resveratrol could be a promising therapeutic option for OA, but more rigorous human studies are needed to confirm its effectiveness in clinical settings.

Article Abstract

Background And Objective: Osteoarthritis (OA) is the most common age-related disease of joints with increasing global prevalence. Persistent inflammation within the joint space is speculated to be the cause of OA. Resveratrol is an anti-inflammatory and antioxidant compound which can influence cartilage metabolism through multiple signalling pathways. This systematic review and meta-analysis aimed to summarize the therapeutic effects of resveratrol in animal models of OA.

Methods: A comprehensive literature search was performed using PubMed, Embase, Web of Science, Cochrane Library, China National Knowledge Infrastructure, China Wanfang and VIP databases in May 2023. Studies on the effects of resveratrol in animal models of OA written in English or Mandarin, published from the inception of databases until the date of the search were considered.

Results: Fifteen eligibility studies were included and analysed. Resveratrol was shown to inhibit the secretion of interleukin-1β, tumour necrosis factor-α, interleukin-6, nitric oxide, and apoptosis of articular chondrocytes. Joint structure as indicated by Mankin scores was restored with resveratrol in animal OA models.

Conclusion: Resveratrol is a potential therapeutic agent for OA based on animal studies. Further evidence from well-planned human studies would be required to validate its clinical efficacies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11269911PMC
http://dx.doi.org/10.1016/j.heliyon.2024.e34064DOI Listing

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