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一种新型苯甲酰胺衍生物通过抑制NFATc1介导的破骨细胞生成来保护结扎诱导的牙槽骨侵蚀。

A novel benzamide derivative protects ligature-induced alveolar bone erosion by inhibiting NFATc1-mediated osteoclastogenesis.

作者信息

Ihn Hye Jung, Lee Taeho, Lee Doohyun, Kim Ju Ang, Kim Kiryeong, Lim Soomin, Kim Jae-Young, Lee Youngkyun, Kim Sang-Hyun, Lee Hyun-Shik, Shin Hong-In, Park Eui Kyun

机构信息

Institute for Hard Tissue and Bio-tooth Regeneration, Kyungpook National University, Daegu 41940, Republic of Korea.

College of Pharmacy, Research Institute of Pharmaceutical Sciences, Kyungpook National University, Daegu 41566, Republic of Korea.

出版信息

Toxicol Appl Pharmacol. 2018 Sep 15;355:9-17. doi: 10.1016/j.taap.2018.06.017. Epub 2018 Jun 20.

Abstract

Since elevated osteoclast formation and/or activity by inhibitory responses against pathogens leads to diverse osteolytic bone diseases including periodontitis, inhibition of osteoclast differentiation and bone resorption has been a primary therapeutic strategy. In this study, we investigated the therapeutic potential of a novel benzamide-linked molecule, OCLI-070, for preventing alveolar bone loss in mice with ligature-induced experimental periodontitis. OCLI-070 inhibited osteoclast formation by acting on both early and late stages of differentiation, and attenuated the induction of nuclear factor of activated T-cells, cytoplasmic 1 (NFATc1) and the expression of osteoclast-specific genes. In addition, OCLI-070 significantly suppressed the formation of actin rings and resorption pits. Analysis of the inhibitory action of OCLI-070 showed that it markedly suppressed receptor activator of nuclear factor-κB ligand (RANKL)-induced extracellular signal-regulated kinase (ERK) and NF-κB signaling cascades. Moreover, OCLI-070 prevented ligature-induced alveolar bone erosion in mice by suppressing osteoclast formation. These findings demonstrate that OCLI-070 attenuated osteoclast differentiation and function as well as ligature-induced bone erosion by inhibiting RANKL-mediated ERK and NF-κB signaling pathways.

摘要

由于针对病原体的抑制性反应导致破骨细胞形成增加和/或活性增强会引发包括牙周炎在内的多种溶骨性骨疾病,因此抑制破骨细胞分化和骨吸收一直是主要的治疗策略。在本研究中,我们研究了一种新型苯甲酰胺连接分子OCLI-070对结扎诱导的实验性牙周炎小鼠牙槽骨丢失的治疗潜力。OCLI-070通过作用于分化的早期和晚期来抑制破骨细胞形成,并减弱活化T细胞核因子细胞质1(NFATc1)的诱导以及破骨细胞特异性基因的表达。此外,OCLI-070显著抑制肌动蛋白环和吸收凹的形成。对OCLI-070抑制作用的分析表明,它显著抑制核因子-κB受体激活剂配体(RANKL)诱导的细胞外信号调节激酶(ERK)和NF-κB信号级联反应。此外,OCLI-070通过抑制破骨细胞形成预防了结扎诱导的小鼠牙槽骨侵蚀。这些发现表明,OCLI-070通过抑制RANKL介导的ERK和NF-κB信号通路减弱了破骨细胞分化和功能以及结扎诱导的骨侵蚀。

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