Laboratory of Histology and Embryology, Faculty of Dental Medicine, University of Monastir, Monastir, Tunisia.
J Periodontol. 2012 Aug;83(8):1063-8. doi: 10.1902/jop.2011.110242. Epub 2011 Dec 13.
Bisphosphonates are indicated for the treatment of osteoporosis. However, they could have an adverse effect on specific sites, such as the bisphosphonate-related osteonecrosis of the jaw. The aim of this study is to investigate the effect of etidronate on the resorption and apposition sides of the periodontium in ovariectomized rats.
Twenty-four female Wistar rats were randomly subjected to either ovariectomy or sham operation. After 8 weeks, six animals of each group were sacrificed. The other 12 rats received 5 mg/kg/day etidronate subcutaneously during 4 weeks. Tartrate-resistant acid phosphatase reaction and immunohistochemical staining for receptor activator of nuclear factor-κB (RANK), RANK-ligand (RANKL), osteoprotegerin (OPG), and osteocalcin was performed. Immunoreactivity was evaluated using a semiquantitative analysis.
In ovariectomized rats, osteoclasts were noticed in the root socket of molars, including the apposition side of the periodontium, in which RANKL expression was significantly evidenced. In the etidronate-treated group, OPG expression was significantly expressed and osteoclasts that were noticed in the resorption side remained undetected in the apposition side even under ovariectomy. RANK was significantly expressed in ovariectomized rats treated with etidronate. Osteoid formation and osteocalcin expression were described on the alveolar bone surfaces in etidronate-treated rats, with or without ovariectomy.
Etidronate has specific site and bone cell actions in the periodontium. It inhibits the osteoclast differentiation induced by ovariectomy in the apposition side of the periodontium but maintains bone formation over all the socket surfaces. Such specificity may be related to the pathogenesis of the bisphosphonate-induced osteonecrosis of the jaw.
双膦酸盐被用于治疗骨质疏松症。然而,它们可能对特定部位产生不良反应,例如双膦酸盐相关性下颌骨坏死。本研究旨在探讨依替膦酸对去卵巢大鼠牙周组织的吸收和形成侧的影响。
24 只雌性 Wistar 大鼠随机接受卵巢切除术或假手术。8 周后,每组 6 只动物被处死。其余 12 只大鼠接受依替膦酸 5mg/kg/天皮下注射 4 周。进行酒石酸抗性酸性磷酸酶反应和核因子-κB 受体激活剂(RANK)、RANK 配体(RANKL)、骨保护素(OPG)和骨钙素的免疫组织化学染色。使用半定量分析评估免疫反应性。
在去卵巢大鼠中,磨牙根槽中可见破骨细胞,包括牙周组织的形成侧,其中 RANKL 表达明显。在依替膦酸治疗组中,OPG 表达明显,即使在去卵巢的情况下,在吸收侧发现的破骨细胞在形成侧仍未被检测到。RANK 在依替膦酸治疗的去卵巢大鼠中表达明显。在依替膦酸治疗的大鼠中,牙槽骨表面有骨样形成和骨钙素表达,无论是否去卵巢。
依替膦酸在牙周组织中有特定的部位和骨细胞作用。它抑制了牙周组织形成侧由去卵巢引起的破骨细胞分化,但维持了所有牙槽骨表面的骨形成。这种特异性可能与双膦酸盐诱导的下颌骨坏死的发病机制有关。