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Medical ozone therapy as a potential treatment modality for regeneration of damaged articular cartilage in osteoarthritis

Osteoarthritis (OA) is the most common degenerative joint disease and a growing health problem affecting more than half of the population over the age of 65. It is characterized by inflammation in the cartilage and synovium, resulting in the loss of joint structure and progressive damage to the cart...

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Detalles Bibliográficos
Autores principales: Manoto, Sello Lebohang, Maepa, Makwese Johaness, Motaung, Shirley Keolebogile
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5935866/
https://www.ncbi.nlm.nih.gov/pubmed/29736142
http://dx.doi.org/10.1016/j.sjbs.2016.02.002
Descripción
Sumario:Osteoarthritis (OA) is the most common degenerative joint disease and a growing health problem affecting more than half of the population over the age of 65. It is characterized by inflammation in the cartilage and synovium, resulting in the loss of joint structure and progressive damage to the cartilage. Many pro-inflammatory mediators are elevated in OA, including reactive oxygen species (ROS) such as nitric oxide (NO) and hydrogen peroxide (H(2)O(2)). Damaged articular cartilage remains a challenge to treat due to the limited self-healing capacity of the tissue and unsuccessful biological interventions. This highlights the need for better therapeutic strategies to heal damaged articular cartilage. Ozone (O(3)) therapy has been shown to have positive results in the treatment of OA; however the use of O(3) therapy as a therapeutic agent is controversial. There is a perception that O(3) is always toxic, whereas evidence indicates that when it is applied following a specified method, O(3) can be effective in the treatment of degenerative diseases. The mechanism of action of O(3) therapy in OA is not fully understood and this review summarizes the use of O(3) therapy in the treatment of damaged articular cartilage in OA.