Renin-angiotensin system in osteoarthritis: A new potential therapy

Yuangang Wu1, Xiaoxi Lu2, Mingyang Li1

  • 1Department of Orthopaedic Surgery, West China Hospital, West China Medical School, Sichuan University, Chengdu 610041, Sichuan Province, China.

Insights

The renin-angiotensin system (RAS) components, including renin, ACE, Ang II, AT1R, and AT2R, contribute to osteoarthritis (OA) by promoting inflammation and chondrocyte hypertrophy. Targeting these RAS elements offers potential new treatments for OA.

Area of Science:

  • Biomedical Science
  • Rheumatology
  • Molecular Biology

Background:

  • Osteoarthritis (OA) is a prevalent chronic joint disease with incompletely understood mechanisms.
  • The renin-angiotensin system (RAS) is crucial for homeostasis and increasingly implicated in OA pathogenesis.

Purpose of the Study:

  • To review and synthesize current research on the association between RAS components and osteoarthritis.
  • To identify potential therapeutic targets within the RAS for OA intervention.

Main Methods:

  • Systematic literature search of major e-medical databases (PubMed, Embase, Medline, Web of Science).
  • Inclusion of English publications detailing the roles of renin, ACE, Ang II, and ATR in OA.
  • Summary of identified signaling pathways involved in RAS-mediated OA.

Main Results:

  • RAS components (renin, ACE, Ang II, AT1R, AT2R) are implicated in OA-related inflammation and chondrocyte hypertrophy.
  • RAS influences OA through signaling pathways such as NF-κB, JNK, VEGFR/Tie-2, and the Axna2/Axna2R axis.
  • These pathways represent potential targets for novel OA treatments.

Conclusions:

  • RAS components play a significant role in the development and progression of osteoarthritis.
  • Targeting the RAS offers a promising avenue for future OA therapeutic strategies.
  • Further research into RAS modulation could lead to significant advancements in OA treatment.

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