Cell and Matrix Research Institute, Kyungpook National University, Daegu 41944, Korea.
Department of Oral Pathology and Regenerative Medicine, School of Dentistry, Institute for Hard Tissue and Bio-tooth Regeneration (IHBR), Kyungpook National University, Daegu 41940, Korea.
Int J Mol Sci. 2021 Aug 2;22(15):8299. doi: 10.3390/ijms22158299.
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.
绝经后骨质疏松症与破骨细胞的过度形成和功能密切相关,导致骨量丢失。已经开发了针对破骨细胞的靶向药物来治疗这种疾病。我们研究了环吡酮胺对体外和体内破骨细胞分化和骨吸收的影响。环吡酮胺显著抑制了核因子 kappa B 受体激活剂配体 (RANKL) 诱导的原代小鼠骨髓巨噬细胞 (BMM) 中的破骨细胞形成,并且与破骨细胞生成和功能相关的基因表达减少。环吡酮胺抑制了肌动蛋白环和吸收坑的形成。对 BMM 中 RANKL 介导的早期信号事件的分析表明,环吡酮胺抑制 IκBα 磷酸化而不影响丝裂原活化蛋白激酶的激活。此外,环吡酮胺的给药抑制了去卵巢诱导的骨质疏松症小鼠中的破骨细胞形成和骨丢失,并降低了血清骨钙素和 I 型胶原 C 末端端肽片段的 C 末端水平。这些结果表明,环吡酮胺在体外和体内均表现出抗破骨细胞生成活性,是预防骨质疏松症和其他与破骨细胞相关的骨疾病的新候选化合物。