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Bupivacaine in combination with sildenafil (Viagra) and vitamin D3 have anti-inflammatory effects in osteoarthritic chondrocytes

AIMS: To treat osteoarthritic chondrocytes and thereby reduce the inflammation with a drug combination that primarily affects 5-HT- and ATP-evoked Ca(2+) signaling. In osteoarthritic chondrocytes, Ca(2+) signaling is elevated, resulting in increased production of ATP and inflammatory mediators. The...

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Detalles Bibliográficos
Autores principales: Hansson, Elisabeth, Skiöldebrand, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8663929/
https://www.ncbi.nlm.nih.gov/pubmed/34909684
http://dx.doi.org/10.1016/j.crphar.2021.100066
Descripción
Sumario:AIMS: To treat osteoarthritic chondrocytes and thereby reduce the inflammation with a drug combination that primarily affects 5-HT- and ATP-evoked Ca(2+) signaling. In osteoarthritic chondrocytes, Ca(2+) signaling is elevated, resulting in increased production of ATP and inflammatory mediators. The expression of TLR4 and Na(+)/K(+)-ATPase was used to evaluate the inflammatory status of the cells. MAIN METHODS: Equine chondrocytes were collected from joints with mild structural osteoarthritic changes and cultured in monolayers. The cells were treated with a combination of bupivacaine (1 pM) and sildenafil (1 ​μM) in combination with vitamin D3 (100 ​nM). A high-throughput screening system, the Flexstation 3 microplate reader, was used to measure intra- and extracellular Ca(2+) signaling after exposure to 5-HT, glutamate, or ATP. Expression of inflammatory receptors was assessed by Western blotting. KEY FINDINGS: Drug treatment substantially reduced 5-HT- and ATP-evoked intracellular Ca(2+) release and TLR4 expression compared to those in untreated chondrocytes. The combination of sildenafil, vitamin D3 together with metformin, as the ability to take up glucose is limited, increased Na(+)/K(+)-ATPase expression. SIGNIFICANCE: The combination of these three therapeutic substances at concentrations much lower than usually used, reduced expression of the inflammatory receptor TLR4 and increased the cell membrane enzyme Na(+)/K(+)-ATPase, which regulates cell volume and reduces increased intracellular Ca(2+) concentrations. These remarkable results indicate that this drug combination has disease-modifying osteoarthritis drug (DMOAD) properties and may be a new clinical therapy for osteoarthritis (OA).