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. 2023 Apr 18;18(3):959–971. doi: 10.1016/j.jds.2023.04.002

Table 6.

Potential therapeutic procedures towards molecules involved in TMJ OA.

Therapeutic Procedures Main Factors Affected Pathways Effects References
Exosome miR-100-5p Attenuating inflammation and ECM degeneration 95
BMSC EVs ATX, YAP HIPPO Inducing cartilage reconstruction 96
Exosome miR-27b-3p Inhibiting M1 polarization 97
LIPUS ZNT-9 Attenuating ECM degeneration 98
LIPUS HIF-1α, HIF-2α Attenuating inflammation and ECM degeneration 99
Curcumin Nrf2, ARE Nrf2/ARE Attenuating inflammation and oxidative stress 100
Hyaluronic acid (HA) NLRP3 Attenuating inflammation 101
Yohimbine Ikkβ, p65 NF-κB Attenuating inflammation 102
Methylprednisolone TNF-α, CRP Attenuating inflammation 103
Glycyrrhizin HMGB1 NF-κB/Akt Attenuating inflammation 104
RAGE/TLR4
Genistein p65 NF-κB Attenuating inflammation 105
Resveratrol COX2, p65 NF-κB Attenuating inflammation and apoptosis 106
Etanercept HIF-2α, EF5 Attenuating pain and hypoxia 107
Rapamycin IL-1β, mTOR, LC3 Wnt/β-catenin Enhancing autophagy 71
Rebamipide RANKL NF-κB, MAPK Inhibiting oxidative stress and osteoclast 108
Strontium ranelate β-catenin Wnt/β-catenin Promoting chondrogenesis 109

Abbreviations: mTOR: mammalian target of rapamycin; BMSC: bone marrow mesenchymal stem cell; EV: extracellular vesicles; ATX: autotaxin; CSF: colony-stimulating factor; ZNT: zinc transporter; MTF: metal responsive transcription factor; HIF: hypoxia-inducible factor; NF-κB: nuclear factor-kappa B; HMGB: high mobility group box protein; Akt: protein kinase B; RAGE: receptor for advanced glycation end products.