Kimura Masakazu, Miyazawa Ken, Tabuchi Masako, Maeda Hatsuhiko, Kameyama Yoichiro, Goto Shigemi
Department of Orthodontics, School of Dentistry, Aichi-Gakuin University, Chikusa-ku, Nagoya 464-8651, Japan.
Calcif Tissue Int. 2008 Feb;82(2):137-47. doi: 10.1007/s00223-007-9097-y. Epub 2008 Jan 4.
Osteoprotegerin (OPG) is a novel secreted member of the tumor necrosis factor receptor family which plays a crucial role in negative regulation of osteoclastic bone resorption. OPG-deficient (OPG-/-) mice develop severe osteoporosis caused by significant enhancement of bone resorption by osteoclasts. We investigated the effect of administering bisphosphonate on mandibular growth and development in OPG-/- mice. Eight-week-old male OPG-/- mice and wild-type (WT) mice were administered bisphosphonate (1.25 mg/kg body weight) intraperitoneally once every 3 days for 30 days. All bone formation-related parameters and bone resorption-related parameters were significantly lower in OPG-/- mice with bisphosphonate than in those without bisphosphonate. The volume of the whole condyle and the mandibular length in OPG-/- mice without bisphosphonate were significantly smaller than in WT mice without bisphosphonate. Bisphosphonate treatment of the OPG-/- mice resulted in an increase in the volume of the mandibular condyle and mandibular ramus length. In fact, the mandibular ramus length in OPG-/- mice with bisphosphonate was similar to the length in WT mice without bisphosphonate. Histologically, the surface irregularity of the mandibular condyle that was observed in the OPG-/- mice without bisphosphonate tended to be less marked in the OPG-/- mice with bisphosphonate, and the proportion of the area of the cartilage layer relative to the whole condyle was significantly larger in OPG-/- mice with bisphosphonate than in those without bisphosphonate. In conclusion, bisphosphonate treatment results in an increase in mandibular condylar dimensions and normalization of mandibular ramus growth.
骨保护素(OPG)是肿瘤坏死因子受体家族新发现的分泌型成员,在破骨细胞介导的骨吸收负调控中起关键作用。OPG基因缺陷(OPG-/-)小鼠因破骨细胞介导的骨吸收显著增强而发生严重骨质疏松。我们研究了双膦酸盐给药对OPG-/-小鼠下颌骨生长发育的影响。8周龄雄性OPG-/-小鼠和野生型(WT)小鼠每3天腹腔注射一次双膦酸盐(1.25 mg/kg体重),共30天。与未使用双膦酸盐的OPG-/-小鼠相比,使用双膦酸盐的OPG-/-小鼠所有与骨形成相关的参数和与骨吸收相关的参数均显著降低。未使用双膦酸盐的OPG-/-小鼠的整个髁突体积和下颌骨长度显著小于未使用双膦酸盐的WT小鼠。对OPG-/-小鼠进行双膦酸盐治疗后,下颌髁突体积和下颌支长度增加。事实上,使用双膦酸盐的OPG-/-小鼠的下颌支长度与未使用双膦酸盐的WT小鼠的长度相似。组织学上,未使用双膦酸盐的OPG-/-小鼠下颌髁突表面的不规则性在使用双膦酸盐的OPG-/-小鼠中往往不那么明显,并且使用双膦酸盐的OPG-/-小鼠软骨层面积相对于整个髁突的比例显著大于未使用双膦酸盐的小鼠。总之,双膦酸盐治疗可增加下颌髁突尺寸并使下颌支生长正常化。