Inhibition of 12/15-lipoxygenase reduces orthodontically induced root resorption in rats

Yukako Nashiro-Oyakawa, Y. Hotokezaka, H. Hotokezaka, Takeshi Moriishi, Mariko Funaki-Dohi, Yosuke Iuchi, Mizuki Ohama, Y. Morita, Noriaki Yoshida
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Abstract

To investigate whether the inhibition of 12/15-lipoxygenase (12/15-LOX), one of the core enzymes of the arachidonic acid cascade, suppresses orthodontically induced root resorption (OIRR), and examine the involvement of the hyaline degeneration of periodontal ligament cells and odontoclast differentiation. The left maxillary first molars of 10-week-old male Wistar rats were moved mesially for 14 days using a closed-coil spring (25 cN) inserted between the first molar and incisor. The rats were intraperitoneally administered with a 12/15-LOX specific inhibitor (ML-351; 0.05 mmol/kg) daily in the experimental group or vehicle (dimethyl sulfoxide) in the control group. Tooth movement was measured using microcomputed tomography on day 14. The appearance of OIRR, hyaline degeneration, osteoclasts, and odontoclasts was evaluated via histological analysis. Immunohistochemical staining for receptor-activated NF-kB ligand (RANKL) and osteoprotegerin was performed. OIRR observed on day 14 in the control group was strongly suppressed by ML-351 treatment. Hyaline degeneration observed on the compression side on day 3 and the appearance of osteoclasts and odontoclasts on days 3 and 14 were significantly suppressed by ML-351. RANKL expression on day 3 was significantly suppressed by ML-351. These key processes in OIRR were substantially suppressed by ML-351 treatment. Inhibition of 12/15-LOX reduced OIRR by suppressing hyaline degeneration and subsequent odontoclast differentiation.
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抑制 12/15 脂氧合酶可减少正畸诱导的大鼠牙根吸收
研究花生四烯酸级联反应的核心酶之一 12/15 脂氧合酶(12/15-LOX)的抑制作用是否能抑制正畸诱导的牙根吸收(OIRR),并探讨牙周韧带细胞透明变性和牙髓分化的参与作用。 使用插入第一臼齿和切牙之间的闭合卷簧(25 cN),将 10 周大雄性 Wistar 大鼠的左上颌第一臼齿向中线移动 14 天。实验组大鼠每天腹腔注射 12/15-LOX 特异性抑制剂(ML-351;0.05 mmol/kg),对照组大鼠每天腹腔注射载体(二甲亚砜)。第14天使用显微计算机断层扫描测量牙齿移动情况。通过组织学分析评估 OIRR、透明变性、破骨细胞和牙髓细胞的外观。对受体激活的 NF-kB 配体(RANKL)和骨保护蛋白进行了免疫组化染色。 对照组在第 14 天观察到的 OIRR 被 ML-351 治疗强烈抑制。ML-351 能显著抑制第 3 天在受压侧观察到的透明变性,以及第 3 天和第 14 天出现的破骨细胞和破牙细胞。ML-351 还显著抑制了第 3 天 RANKL 的表达。ML-351 的处理大大抑制了 OIRR 的这些关键过程。 抑制 12/15-LOX 可抑制透明变性和随后的牙髓分化,从而减少 OIRR。
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