Local delivery of osteoprotegerin inhibits mechanically mediated bone modeling in orthodontic tooth movement

被引:95
作者
Dunn, Matthew D.
Park, Chan Ho
Kostenuik, Paul J.
Kapila, Sunil
Giannobile, William V.
机构
[1] Univ Michigan, Sch Dent, Dept Orthodont & Peadiat Dent, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Dent, Dept Periodont & Oral Med, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Sch Dent, Ctr Craniofacial Regenerat, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Coll Engn, Dept Biomed Engn, Ann Arbor, MI 48109 USA
[5] Amgen Inc, Metab Dis Res, Thousand Oaks, CA USA
[6] Michigan Ctr Oral Hlth Res, Ann Arbor, MI 48106 USA
关键词
RANKL inhibitor; OPG; osteoclast; micro-computed tomography; tooth movement;
D O I
10.1016/j.bone.2007.04.194
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: The RANKL-OPG axis is a key regulator of osteoclastogenesis and bone turnover activity. Its contribution to bone resorption under altered mechanical states, however, has not been fully elucidated. Here we examined the role of OPG in regulating mechanically induced bone modeling in a rat model of orthodontic tooth movement. Methods: The maxillary first molars of male Sprague-Dawley rats were moved mesially using a calibrated nickel-titanium spring attached to the maxillary incisor teeth. Two different doses (0.5 mg/kg, 5.0 mg/kg) of a recombinant fusion protein (OPG-Fc), were injected twice weekly mesial to the first molars. Tooth movement was measured using stone casts that were scanned and magnified. Changes in bone quantity were measured using micro-computed tomography and histomorphometric analysis was used to quantify osteoclasts and volumetric parameters. Finally, circulating levels of TRAP-5b (a bone resorption marker) was measured using enzyme-linked immunosorbent assay. Results: The 5.0 mg/kg OPG-Fc dose showed a potent reduction in mesial molar movement and osteoclast numbers compared to controls (p <0.01). The molar movement was inhibited by 45.7%, 70.6%, and 78.7% compared to controls at days 7, 14, and 21 respectively, with the high dose of OPG. The 0.5 mg dose also significantly (p<0.05) inhibited molar movement at days 7 (43.8%) and 14 (31.8%). While incisor retraction was also decreased by OPG-Fc, the ratio of incisor to molar tooth movement was markedly better in the high-dose OPG group (5.2:1, p<0.001) compared to the control group (2.3:1) and the low-dose OPG group (2.0:1). Conclusions: Local delivery of OPG-Fc inhibits osteoclastogenesis and tooth movement at targeted dental sites. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:446 / 455
页数:10
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