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August 20, 2026Journal of Visualized Experiments0 citationsOpen Access

Acupotomy Regulates the RIC8A/P38 MAPK Axis Based on the CircRNA Scaffold to Promote Cartilage Repair in Knee Osteoarthritis

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GLGuo-Rui LuanXSXiang ShangHZHan-Qing Zhao

Key Points

  • To evaluate the therapeutic efficacy and underlying molecular mechanism of acupotomy in treating knee osteoarthritis through the circPDE4B/RIC8A/p38 MAPK signaling axis in a rabbit model.
  • Fifty New Zealand White rabbits were randomly assigned to five groups (n = 10 per group): control, KOA model (induced via the modified Videman method), celecoxib (24 mg/kg daily by gavage), acupotomy (once weekly), and sham acupotomy for 4 weeks.
  • Assessed knee swelling, cartilage histopathology, inflammatory cytokines (IL-1β, TNF-α, IL-6) via ELISA, and cartilage metabolism genes and pathway proteins via qRT-PCR and Western blotting.
  • Acupotomy significantly reduced knee swelling, improved cartilage histopathological scores, and lowered inflammatory cytokine levels (IL-1β, TNF-α, and IL-6) compared to untreated KOA model controls.
  • Acupotomy upregulated circPDE4B, SOX9, and aggrecan, while downregulating MMP-3, MMP-13, RIC8A, and phosphorylated p38 MAPK to levels comparable to celecoxib, whereas sham acupotomy showed no significant improvement.

Abstract

Knee osteoarthritis (KOA) is characterized by progressive cartilage degeneration and inflammation. This study investigated the therapeutic effects of acupotomy in a rabbit model of KOA and its association with the circular RNA phosphodiesterase 4B (circPDE4B)/resistance to inhibitors of cholinesterase 8A (RIC8A)/p38 mitogen-activated protein kinase (MAPK) signaling axis. Fifty New Zealand White rabbits were randomly assigned to five groups (n = 10 per group): control, KOA model, celecoxib, acupotomy, and sham acupotomy. KOA was induced using the modified Videman method. Beginning 6 weeks after modeling, acupotomy was administered once weekly for 4 weeks, whereas celecoxib was administered daily by gavage at 24 mg/kg for 4 weeks. Knee swelling and cartilage histopathology were evaluated. Levels of interleukin-1β (IL-1β) , tumor necrosis factor-α (TNF-α) , and interleukin-6 (IL-6) in cartilage tissue homogenates were measured by enzyme-linked immunosorbent assay. Gene and protein expression associated with cartilage metabolism and the circPDE4B/RIC8A/p38 MAPK axis were assessed by quantitative reverse transcription polymerase chain reaction and Western blotting. Compared with the KOA model group, acupotomy reduced knee swelling, improved histopathological scores, decreased inflammatory cytokine levels, downregulated matrix metalloproteinase-3 (MMP-3) , matrix metalloproteinase-13 (MMP-13), RIC8A, and phosphorylated p38 MAPK, and upregulated SRY-box transcription factor 9 (SOX9), aggrecan, and relative circPDE4B. Its effects were comparable to those of celecoxib, whereas sham acupotomy produced no significant improvement. These findings indicate that acupotomy alleviates inflammation and cartilage degeneration in rabbit KOA and is associated with modulation of the circPDE4B/RIC8A/p38 MAPK axis.

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Cite This Study

Luan et al. (2026) studied this question.

synapsesocial.com/papers/6a86b5178a91293e6a1cc5bchttps://doi.org/10.3791/71422
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Acupotomy Ameliorates Articular Cartilage Fibrosis in a Rabbit Model of Knee Osteoarthritis via the TGF-β1/Smad Pathway2026
  2. 2Acupotomy ameliorates knee osteoarthritis-related collagen deposition and fibrosis in rabbit skeletal muscle through the TGF-β/Smad pathway2024
  3. 3Mechanism of acupoint penetration acupuncture therapy regulating chondrocyte autophagy via the PI3K/Akt-mTOR pathway in KOA rats2024 · 2 citations
  4. 4[Effect of acupuncture on chondrocyte autophagy in rats of knee osteoarthritis based on PI3K/Akt/mTOR signaling pathway].2025
  5. 5Adipose‐derived mesenchymal stem cell injection into the KI10 acupoint mitigates cartilage damage in KOA rats through PGE2 ‐mediated α7nAChR / NF ‐ κB pathway2026