Hadaya Danny, Soundia Akrivoula, Gkouveris Ioannis, Dry Sarah M, Aghaloo Tara L, Tetradis Sotirios
Graduate Student, Division of Diagnostic and Surgical Sciences, UCLA School of Dentistry, Los Angeles, CA.
Post-doctoral Fellow, Division of Diagnostic and Surgical Sciences, UCLA School of Dentistry, Los Angeles, CA.
J Oral Maxillofac Surg. 2019 Jan;77(1):71-86. doi: 10.1016/j.joms.2018.08.010. Epub 2018 Aug 22.
Medication-related osteonecrosis of the jaw (MRONJ) is a rare but severe side effect of antiresorptive medications. Most animal models use tooth extraction as an instigating local factor to induce MRONJ, with varied results. However, these teeth are healthy and absent of dental disease, a rare finding that does not reflect clinical practices. The authors hypothesized that extraction of teeth with periapical inflammation would lead to MRONJ in rats treated with high-dose bisphosphonates.
Rats were pretreated with zoledronic acid (ZA) for 1 week. Pulp exposure (PE) was established by exposing the pulpal chamber of the first and second molars. Experimental periapical disease (EPD) was induced by PE and bacterial inoculation into pulp chambers of the first and second mandibular molars. The mandibular molars were extracted 4 weeks after PE or EPD, and animals were euthanized 4 weeks after tooth extraction. Extraction sockets were assessed clinically, radiographically, and histologically.
Clinically, radiographically, and histologically, socket healing was observed in all vehicle-treated animals and in ZA-treated animals after extraction of healthy teeth or teeth with PE. In contrast, bone exposure, lack of socket healing, and osteonecrosis were present in most ZA-treated animals after extraction of teeth with EPD. Bacterial presence was noted in areas of osteonecrotic alveolar bone.
These data support a synergistic contribution of severe dental disease and tooth extraction to MRONJ pathogenesis. Importantly, this model is amenable to manipulation of methodologic conditions for the dissection of parameters involved in MRONJ pathogenesis.
药物相关性颌骨坏死(MRONJ)是抗吸收药物一种罕见但严重的副作用。大多数动物模型使用拔牙作为诱发局部因素来诱导MRONJ,结果各异。然而,这些牙齿是健康的且无牙科疾病,这一罕见情况并不反映临床实际。作者推测,拔除患有根尖周炎的牙齿会导致高剂量双膦酸盐治疗的大鼠发生MRONJ。
大鼠用唑来膦酸(ZA)预处理1周。通过暴露第一和第二磨牙的髓腔建立牙髓暴露(PE)。通过PE和将细菌接种到第一和第二下颌磨牙的髓腔诱导实验性根尖周病(EPD)。在PE或EPD后4周拔除下颌磨牙,拔牙后4周对动物实施安乐死。对拔牙创进行临床、影像学和组织学评估。
在临床、影像学和组织学上,所有接受赋形剂治疗的动物以及拔除健康牙齿或患有PE牙齿后的ZA治疗动物的拔牙创均观察到愈合。相比之下,拔除患有EPD牙齿后的大多数ZA治疗动物出现骨暴露、拔牙创未愈合和骨坏死。在骨坏死的牙槽骨区域发现有细菌存在。
这些数据支持严重牙科疾病和拔牙对MRONJ发病机制有协同作用。重要的是,该模型适合于操纵方法学条件以剖析MRONJ发病机制中涉及的参数。