| Literature DB >> 34361069 |
Hye Jung Ihn1, Jiwon Lim2, Kiryeong Kim2, Sang-Hyeon Nam2, Soomin Lim2, Su Jeong Lee2, Jong-Sup Bae3, Tae Hoon Kim4, Jung-Eun Kim5, Moon-Chang Baek5, Yong Chul Bae6, Eui Kyun Park2.
Abstract
Postmenopausal osteoporosis is closely associated with excessive osteoclast formation and function, resulting in the loss of bone mass. Osteoclast-targeting agents have been developed to manage this disease. We examined the effects of ciclopirox on osteoclast differentiation and bone resorption in vitro and in vivo. Ciclopirox significantly inhibited osteoclast formation from primary murine bone marrow macrophages (BMMs) in response to receptor activator of nuclear factor kappa B ligand (RANKL), and the expression of genes associated with osteoclastogenesis and function was decreased. The formation of actin rings and resorption pits was suppressed by ciclopirox. Analysis of RANKL-mediated early signaling events in BMMs revealed that ciclopirox attenuates IκBα phosphorylation without affecting mitogen-activated protein kinase activation. Furthermore, the administration of ciclopirox suppressed osteoclast formation and bone loss in ovariectomy-induced osteoporosis in mice and reduced serum levels of osteocalcin and C-terminal telopeptide fragment of type I collagen C-terminus. These results indicate that ciclopirox exhibits antiosteoclastogenic activity both in vitro and in vivo and represents a new candidate compound for protection against osteoporosis and other osteoclast-related bone diseases.Entities:
Keywords: bone resorption; ciclopirox; osteoclast; osteoporosis
Year: 2021 PMID: 34361069 DOI: 10.3390/ijms22158299
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923