Benzydamine inhibits osteoclast differentiation and bone resorption via down-regulation of interleukin-1β expression

Bone diseases such as osteoporosis and periodontitis are induced by excessive osteoclastic activity, which is closely associated with inflammation. Benzydamine (BA) has been used as a cytokine-suppressive or non-steroidal anti-inflammatory drug that inhibits the production of pro-inflammatory cytokines or prostaglandins. However, its role in osteoclast differentiation and function remains unknown. Here, we explored the role of BA in regulating osteoclast differentiation and elucidated the underlying mechanism. BA inhibited osteoclast differentiation and strongly suppressed interleukin-1 beta (IL-1 beta) production. BA inhibited osteoclast formation and bone resorption when added to bone marrow-derived macrophages and differentiated osteoclasts, and the inhibitory effect was reversed by IL-1 beta treatment. The reporter assay and the inhibitor study of IL-1 beta transcription suggested that BA inhibited nuclear factor-kappa B and activator protein-1 by regulating I kappa B kinase, extracellular signal regulated kinase and P38, resulting in the down-regulation of IL-1 beta expression. BA also promoted osteoblast differentiation. Furthermore, BA protected lipopolysaccharide-and ovariectomy-induced bone loss in mice, suggesting therapeutic potential against inflammation-induced bone diseases and postmenopausal osteoporosis. (C) 2020 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V.