Division of Orthodontics and Dentofacial Orthopedics, Tohoku University Graduate School of Dentistry, Sendai, Miyagi, Japan.
Frontier Research Institute for Interdisciplinary Sciences, Tohoku University, Sendai, Miyagi, Japan.
Front Immunol. 2023 Jan 18;13:929690. doi: 10.3389/fimmu.2022.929690. eCollection 2022.
Docosahexaenoic acid (DHA) is an omega-3 fatty acid that has a range of positive impacts on human health, including anti-inflammatory effects and inhibition of osteoclast formation G-protein-coupled receptor 120 (GPR120). Orthodontic force was reported to induce tumor necrosis factor-α (TNF-α) expression, which activates osteoclast differentiation during orthodontic tooth movement (OTM). The aim of this study was to investigate the influence of DHA on TNF-α-induced osteoclast formation and OTM . We examined osteoclast formation and bone resorption within the calvaria of both wild-type (WT) and GPR120-deficient (GPR120-KO) mice injected with phosphate-buffered saline (PBS), TNF-α, TNF-α and DHA, or DHA. DHA inhibited TNF-α-induced osteoclast formation and bone resorption in WT mice but had no effect in GPR120-KO mice. OTM experiments were performed in mouse strains with or without regular injection of DHA, and the effects of DHA on osteoclast formation in the alveolar bones during OTM were examined. DHA also suppressed OTM in WT but not GPR120-KO mice. Our data showed that DHA suppresses TNF-α-induced osteoclastogenesis and bone resorption GPR120. TNF-α has considerable significance in OTM, and therefore, DHA may also inhibit TNF-α-induced osteoclast formation and bone resorption in OTM.
二十二碳六烯酸 (DHA) 是一种 ω-3 脂肪酸,对人类健康有一系列积极影响,包括抗炎作用和抑制破骨细胞形成 G 蛋白偶联受体 120 (GPR120)。据报道,正畸力会诱导肿瘤坏死因子-α (TNF-α) 的表达,从而在正畸牙齿移动 (OTM) 期间激活破骨细胞分化。本研究旨在探讨 DHA 对 TNF-α 诱导的破骨细胞形成和 OTM 的影响。我们检查了注射磷酸盐缓冲液 (PBS)、TNF-α、TNF-α 和 DHA 或 DHA 的野生型 (WT) 和 GPR120 缺陷型 (GPR120-KO) 小鼠颅骨中的破骨细胞形成和骨吸收。DHA 抑制了 WT 小鼠中 TNF-α 诱导的破骨细胞形成和骨吸收,但在 GPR120-KO 小鼠中没有作用。在有或没有定期注射 DHA 的小鼠品系中进行了 OTM 实验,并检查了 DHA 对 OTM 期间牙槽骨中破骨细胞形成的影响。DHA 还抑制了 WT 但不抑制 GPR120-KO 小鼠的 OTM。我们的数据表明,DHA 抑制了 TNF-α 诱导的破骨细胞生成和骨吸收 GPR120。TNF-α 在 OTM 中具有相当重要的意义,因此,DHA 也可能抑制 OTM 中 TNF-α 诱导的破骨细胞形成和骨吸收。