Abstract
This study aims to evaluate the therapeutic potential of cuprorivaite microspheres for osteoarthritis (OA), in particular, potential molecular mechanisms were investigated. The microspheres were developed from Ca(NO3)2•4H2O, Cu(NO3)2•3H2O, and silica gel, and further therapeutic effects were tested in vitro on mouse primary chondrocytes treated with interleukin-1β (IL-1β) to mimic OA, and in vivo on OA mice induced via anterior cruciate ligament transection (ACLT) surgery. The microspheres were shown to mitigate IL-1β-induced apoptotic, inflammatory, and oxidative stress markers while enhancing cell viability and extracellular matrix (ECM) components in chondrocytes. Moreover, the microspheres ameliorated histopathological damage, reduced inflammatory and oxidative stress markers, and enhanced ECM biomarker levels in OA mice, implicating their role in suppressing cuproptosis and oxidative stress. The aforementioned effects of the cuprorivaite microspheres were demonstrated by using SKL2001, an agonist of the Wnt/β-catenin pathway. The results suggest cuprorivaite microspheres as a promising intervention for OA and cartilage regeneration, highlighting their therapeutic effects on cellular and molecular levels.
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