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山奈酚 3-O-新橙皮糖苷通过破骨细胞生成促进牙萌出过程中被覆盖牙骨质的吸收。

Isorhamnetin 3-O-neohesperidoside promotes the resorption of crown-covered bone during tooth eruption by osteoclastogenesis.

机构信息

Department of Oral Surgery, Ninth People's Hospital, College of Stomatology, Shanghai Jiao Tong University School of Medicine, Shanghai Key Laboratory of Stomatology & Shanghai Research Institute of Stomatology, Shanghai, People's Republic of China.

Department of Endodontics, Jinan Stomatological Hospital, Jinan, Shandong, 250001, People's Republic of China.

出版信息

Sci Rep. 2020 Mar 20;10(1):5172. doi: 10.1038/s41598-020-62107-7.

Abstract

Delayed resorption of crown-covered bone is a critical cause of delayed tooth eruption. Traditional herbal medicines may be good auxiliary treatments to promote the resorption of crown-covered bone. This study was carried out to analyse the effect of isorhamnetin 3-O-neohesperidoside on receptor activator of nuclear factor-kB ligand (RANKL)-induced osteoclastogenesis in vitro and resorption of the crown-covered bone of the lower first molars in mice in vivo. Isorhamnetin 3-O-neohesperidoside promoted osteoclastogenesis and the bone resorption of mouse bone marrow macrophages (BMMs) and upregulated mRNA expression of the osteoclast-specific genes cathepsin K (CTSK), vacuolar-type H + -ATPase d2(V-ATPase d2), tartrate resistant acid phosphatase (TRAP) and nuclear factor of activated T-cells cytoplasmic 1 (NFATc1). NFATc1, p38 and AKT signalling was obviously activated by isorhamnetin 3-O-neohesperidoside in osteoclastogenesis. Isorhamnetin 3-O-neohesperidoside aggravated resorption of crown-covered bone in vivo. In brief, isorhamnetin 3-O-neohesperidoside might be a candidate adjuvant therapy for delayed intraosseous eruption.

摘要

牙冠骨吸收延迟是牙齿迟萌的关键原因。传统草药可能是促进牙冠骨吸收的良好辅助治疗方法。本研究旨在分析山柰酚 3-O-新橙皮糖苷对核因子κB 受体激活剂配体(RANKL)诱导的体外破骨细胞发生和体内小鼠下第一磨牙牙冠骨吸收的影响。山柰酚 3-O-新橙皮糖苷促进了破骨细胞形成和小鼠骨髓巨噬细胞(BMMs)的骨吸收,并上调了破骨细胞特异性基因组织蛋白酶 K(CTSK)、液泡型 H+ -ATP 酶 d2(V-ATPase d2)、抗酒石酸酸性磷酸酶(TRAP)和激活 T 细胞核因子 1(NFATc1)的 mRNA 表达。在破骨细胞发生过程中,山柰酚 3-O-新橙皮糖苷明显激活了 NFATc1、p38 和 AKT 信号通路。山柰酚 3-O-新橙皮糖苷加重了体内牙冠骨的吸收。总之,山柰酚 3-O-新橙皮糖苷可能是一种治疗牙内萌出延迟的候选辅助治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd5b/7083939/ce835dc69f8a/41598_2020_62107_Fig1_HTML.jpg

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