Narmada Ida Bagus, Putri Paristyawati Dwi, Lucynda Lucky, Triwardhani Ari, Ardani I Gusti Aju Wahju, Nugraha Alexander Patera
Department of Orthodontics, Faculty of Dental Medicine, Universitas Airlangga, Surabaya, Indonesia.
Eur J Dent. 2021 May;15(2):295-301. doi: 10.1055/s-0040-1718640. Epub 2021 Jan 28.
To investigate the effect of caffeic acid phenethyl ester (CAPE) provision on matrix metalloproteinase-9 (MMP-9), fibroblast growth factor-2 (FGF-2) expression, osteoclast and osteoblast numbers during experimental orthodontic tooth movement (OTM) in male Wistar rats ().
Forty-eight healthy male Wistar rats (), 16 to 20 weeks old with 200 to 250 g body weight (bw) were divided into several groups as follows: K1: OTM for 3 days; K2: OTM for 7 days; K3: OTM for 14 days; KP1: OTM and CAPE for 3 days; KP2: OTM and CAPE for 7 days; and KP3: OTM and CAPE for 14 days. A nickel titanium closed coil spring 8.0 mm long with 10 g/mm was installed between the upper left first molar and upper central incisor to move molar mesially. CAPE provision with a dose of 20 mg/kg bw of animal studies was done per orally. Immunohistochemistry was done to examine MMP-9 expression and osteoclast number in compression side as well as FGF-2 expression and osteoblast number in tensile side of the OTM.
One-way analysis of variance test and Tukey's honest significant difference test were performed to determine the difference between the groups ( < 0.05).
MMP-9 expression and osteoclast numbers in the compression side were significantly different between the groups. Similarly, FGF-2 expression and osteoclast numbers in the tensile side were significantly different between the groups.
CAPE provision during OTM increases the number of osteoblasts and the FGF-2 expression significantly in the tensile side. Osteoclast numbers and MMP-9 expression significantly decrease in the compression side.
研究在雄性Wistar大鼠实验性正畸牙移动(OTM)过程中,给予咖啡酸苯乙酯(CAPE)对基质金属蛋白酶-9(MMP-9)、成纤维细胞生长因子-2(FGF-2)表达以及破骨细胞和成骨细胞数量的影响。
将48只健康雄性Wistar大鼠(16至20周龄,体重200至250克)分为以下几组:K1组:正畸牙移动3天;K2组:正畸牙移动7天;K3组:正畸牙移动14天;KP1组:正畸牙移动并给予CAPE 3天;KP2组:正畸牙移动并给予CAPE 7天;KP3组:正畸牙移动并给予CAPE 14天。在左上第一磨牙和上中切牙之间安装一个8.0毫米长、弹力为10克/毫米的镍钛闭合螺旋弹簧,使磨牙向近中移动。按照20毫克/千克体重的剂量对动物进行口服CAPE给药。采用免疫组织化学方法检测正畸牙移动压缩侧的MMP-9表达和破骨细胞数量,以及拉伸侧的FGF-2表达和成骨细胞数量。
采用单因素方差分析和Tukey真实显著性差异检验来确定组间差异(P<0.05)。
各组间压缩侧的MMP-9表达和破骨细胞数量存在显著差异。同样,各组间拉伸侧的FGF-2表达和破骨细胞数量也存在显著差异。
在正畸牙移动过程中给予CAPE可显著增加拉伸侧的成骨细胞数量和FGF-2表达。压缩侧的破骨细胞数量和MMP-9表达显著降低。