Bildt M M, Henneman S, Maltha J C, Kuijpers-Jagtman A M, Von den Hoff J W
Radboud University Nijmegen Medical Centre, Department of Orthodontics & Oral Biology, Philips van Leydenlaan 25, Nijmegen, Netherlands.
Arch Oral Biol. 2007 Jun;52(6):571-8. doi: 10.1016/j.archoralbio.2006.11.009. Epub 2006 Dec 15.
Orthodontic tooth movement requires extensive remodeling of the periodontal ligament (PDL) and the alveolar bone. Osteoclasts resorb bone, allowing teeth to migrate in the direction of the force. Matrix metalloproteinases (MMPs) are able to degrade the extracellular matrix of the periodontal tissues. Chemically modified tetracyclines (CMTs) can inhibit MMPs, but lack antimicrobial activity. We hypothesize that CMT-3 will decrease the rate of orthodontic tooth movement in the rat.
Eighteen Wistar rats received a standardized orthodontic appliance at one side of the maxilla. During 14 days, three groups of six rats received a daily dose of 0, 6 or 30mg/kg CMT-3, and tooth displacement was measured. Thereafter, osteoclasts were counted on histological sections using an ED-1 staining. Multi- and mononuclear ED-1-positive cells in the PDL were also counted. In addition, sections were stained for MMP-9.
CMT-3 significantly inhibited tooth movement (p=0.03) and also decreased the number of osteoclasts at the compression sides in the 30mg/kg group (p<0.05). Significantly more mono- than multinuclear ED-1-positive cells were present in the PDL, but no significant differences were found between the dosage groups. Osteoclasts in the 30mg/kg group seemed to contain less MMP-9 than in the control.
CMT-3 inhibits tooth movement in the rat, probably by reducing the number of osteoclasts at the compression side. This might be due to induction of apoptosis in activated osteoclasts or reduced osteoclast migration. Reduced MMP activity by CMT-3 might also directly inhibit degradation of the organic bone matrix.
正畸牙齿移动需要牙周膜(PDL)和牙槽骨进行广泛的重塑。破骨细胞吸收骨质,使牙齿能够沿着力的方向移动。基质金属蛋白酶(MMPs)能够降解牙周组织的细胞外基质。化学修饰四环素(CMTs)可抑制MMPs,但缺乏抗菌活性。我们假设CMT-3会降低大鼠正畸牙齿移动的速率。
18只Wistar大鼠在上颌一侧接受标准化正畸矫治器。在14天内,三组大鼠(每组6只)每日分别给予0、6或30mg/kg的CMT-3,测量牙齿移位情况。此后,使用ED-1染色在组织学切片上计数破骨细胞。还对牙周膜中多核和单核ED-1阳性细胞进行计数。此外,切片进行MMP-9染色。
CMT-3显著抑制牙齿移动(p = 0.03),并且在30mg/kg组中,压缩侧的破骨细胞数量也减少(p < 0.05)。牙周膜中单核ED-1阳性细胞明显多于多核细胞,但各剂量组之间未发现显著差异。30mg/kg组的破骨细胞所含MMP-9似乎比对照组少。
CMT-3抑制大鼠牙齿移动,可能是通过减少压缩侧破骨细胞的数量。这可能是由于激活的破骨细胞凋亡诱导或破骨细胞迁移减少所致。CMT-3降低MMP活性也可能直接抑制有机骨基质的降解。