Tássia T Machado, Ana Carolina S Machado, Catarine M Nishijima, Cleverton Roberto de Andrade, Sílvio Roberto Consonni, Lizandra M de Sousa, Carlos A Parada, Cláudia H Tambeli
{"title":"臭氧治疗对颞下颌关节骨性关节炎软骨退变的保护作用。","authors":"Tássia T Machado, Ana Carolina S Machado, Catarine M Nishijima, Cleverton Roberto de Andrade, Sílvio Roberto Consonni, Lizandra M de Sousa, Carlos A Parada, Cláudia H Tambeli","doi":"10.1007/s10787-025-01904-w","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":13551,"journal":{"name":"Inflammopharmacology","volume":" ","pages":"5333-5345"},"PeriodicalIF":5.3000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Protective effects of ozone therapy on cartilage degeneration in temporomandibular joint osteoarthritis.\",\"authors\":\"Tássia T Machado, Ana Carolina S Machado, Catarine M Nishijima, Cleverton Roberto de Andrade, Sílvio Roberto Consonni, Lizandra M de Sousa, Carlos A Parada, Cláudia H Tambeli\",\"doi\":\"10.1007/s10787-025-01904-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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. 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Protective effects of ozone therapy on cartilage degeneration in temporomandibular joint osteoarthritis.
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.
期刊介绍:
Inflammopharmacology is the official publication of the Gastrointestinal Section of the International Union of Basic and Clinical Pharmacology (IUPHAR) and the Hungarian Experimental and Clinical Pharmacology Society (HECPS). Inflammopharmacology publishes papers on all aspects of inflammation and its pharmacological control emphasizing comparisons of (a) different inflammatory states, and (b) the actions, therapeutic efficacy and safety of drugs employed in the treatment of inflammatory conditions. The comparative aspects of the types of inflammatory conditions include gastrointestinal disease (e.g. ulcerative colitis, Crohn''s disease), parasitic diseases, toxicological manifestations of the effects of drugs and environmental agents, arthritic conditions, and inflammatory effects of injury or aging on skeletal muscle. The journal has seven main interest areas:
-Drug-Disease Interactions - Conditional Pharmacology - i.e. where the condition (disease or stress state) influences the therapeutic response and side (adverse) effects from anti-inflammatory drugs. Mechanisms of drug-disease and drug disease interactions and the role of different stress states
-Rheumatology - particular emphasis on methods of measurement of clinical response effects of new agents, adverse effects from anti-rheumatic drugs
-Gastroenterology - with particular emphasis on animal and human models, mechanisms of mucosal inflammation and ulceration and effects of novel and established anti-ulcer, anti-inflammatory agents, or antiparasitic agents
-Neuro-Inflammation and Pain - model systems, pharmacology of new analgesic agents and mechanisms of neuro-inflammation and pain
-Novel drugs, natural products and nutraceuticals - and their effects on inflammatory processes, especially where there are indications of novel modes action compared with conventional drugs e.g. NSAIDs
-Muscle-immune interactions during inflammation [...]