Machado Tássia T, Machado Ana Carolina S, Nishijima Catarine M, de Andrade Cleverton Roberto, Consonni Sílvio Roberto, de Sousa Lizandra M, Parada Carlos A, Tambeli Cláudia H
Department of Functional and Structural Biology, Institute of Biology, Pain Studies Lab, State University of Campinas (UNICAMP), Rua Carl Von Linnaeus-Cidade Universitária, Campinas-São Paulo, 13083-864, Brazil.
Department of Physiology and Pathology, Araraquara School of Dentistry-Paulista State University (FOAr/UNESP), Araraquara, Brazil.
Inflammopharmacology. 2025 Aug 18. doi: 10.1007/s10787-025-01904-w.
Temporomandibular joint osteoarthritis (TMJ-OA) is a condition characterized by progressive cartilage degradation and inflammation, with matrix metalloproteinases (MMPs) playing an important role in these processes. The present study evaluated the effects of ozone therapy on the expression of MMP-2 and MMP-9 and the cartilage preservation in a monosodium iodoacetate (MIA)-induced TMJ-OA rat model. Female Wistar rats were administered a single intra-articular injection of MIA (2 mg/TMJ in 30 µL saline) or saline into the left TMJ. Three days after the MIA injection, rats received two intra-articular injections of an oxygen-ozone mixture (40 µg/mL, 50 µL) administered at a 1-week interval. To perform immunohistochemical analysis, TMJs were collected at days 5 and 12 post-MIA injections (2 days after each injection of the oxygen-ozone mixture) and for histological analysis at days 14 and 21 post-MIA injection. The results suggested that ozone therapy exhibited a protective effect against cartilage degradation on day 14, yet this effect was not observed on day 21 post-MIA injection. Histological evaluation demonstrated partial cartilage preservation, while immunohistochemistry showed that levels of MMP-9 elevated in the condyle by MIA injection were reduced by ozone therapy. Conversely, MMP-2 scores remained unaffected across all experimental groups. The application of ozone therapy did not result in alterations to the type or intensity of the inflammatory infiltrate observed at the degenerative phase of the osteoarthritis. These findings suggest that a brief treatment protocol of ozone therapy, applied during the inflammatory phase, modulates MMP-9 expression and provides transient protection against cartilage degradation in TMJ-OA.
颞下颌关节骨关节炎(TMJ - OA)是一种以软骨进行性退化和炎症为特征的疾病,基质金属蛋白酶(MMPs)在这些过程中起重要作用。本研究评估了臭氧疗法对碘乙酸钠(MIA)诱导的TMJ - OA大鼠模型中MMP - 2和MMP - 9表达以及软骨保存的影响。将雌性Wistar大鼠的左颞下颌关节内单次注射MIA(2 mg/TMJ溶于30 μL盐水中)或生理盐水。MIA注射后3天,大鼠接受两次关节内注射氧气 - 臭氧混合物(40 μg/mL,50 μL),间隔1周。为进行免疫组织化学分析,在MIA注射后第5天和第12天(每次注射氧气 - 臭氧混合物后2天)收集颞下颌关节,在MIA注射后第14天和第21天进行组织学分析。结果表明,臭氧疗法在第14天对软骨退化具有保护作用,但在MIA注射后第21天未观察到这种效果。组织学评估显示部分软骨得以保存,而免疫组织化学显示,臭氧疗法降低了MIA注射导致的髁突中MMP - 9水平升高。相反,所有实验组中MMP - 2评分均未受影响。臭氧疗法的应用并未导致骨关节炎退变阶段观察到的炎性浸润类型或强度发生改变。这些发现表明,在炎症阶段应用的简短臭氧治疗方案可调节MMP - 9表达,并为TMJ - OA中的软骨退化提供短暂保护。