Osteonecrosis of the jaw (ONJ) is a well-recognized complication of antiresorptive medications, such as bisphosphonates (BPs). Although ONJ is most common after tooth extractions in patients receiving high-dose BPs, many patients do not experience oral trauma. Animal models using tooth extractions and high BP doses recapitulate several clinical, radiographic, and histologic findings of ONJ. We and others have reported on rat models of ONJ using experimental dental disease in the absence of tooth extraction. These models emphasize the importance of dental infection/inflammation for ONJ development. Here, we extend our original report in the rat, and present a mouse model of ONJ in the presence of dental disease. Mice were injected with high dose zoledronic acid and pulpal exposure of mandibular molars was performed to induce periapical disease. After 8 weeks, quantitative and qualitative radiographic and histologic analyses of mouse mandibles were done. Periapical lesions were larger in vehicle-treated versus BP-treated mice. Importantly, radiographic features resembling clinical ONJ, including thickening of the lamina dura, periosteal bone deposition, and increased trabecular density, were seen in the drilled site of BP-treated animals. Histologically, osteonecrosis, periosteal thickening, periosteal bone apposition, epithelial migration, and bone exposure were present in the BP-treated animals in the presence of periapical disease. No difference in tartrate-resistant acid phosphatase (TRAP)+ cell numbers was observed, but round, detached, and removed from the bone surface cells were present in BP-treated animals. Although 88% of the BP-treated animals showed areas of osteonecrosis in the dental disease site, only 33% developed bone exposure, suggesting that osteonecrosis precedes bone exposure. Our data further emphasize the importance of dental disease in ONJ development, provide qualitative and quantitative measures of ONJ, and present a novel mouse ONJ model in the absence of tooth extraction that should be useful in further exploring ONJ pathophysiological mechanisms.
Bisphosphonates (BPs), stable analogs of natural occurring pyrophosphates, are potent inhibitors of osteoclastic-mediated bone resorption and have been used for over 30 years to treat postmenopausal osteoporosis, Paget's disease, hypercalcemia of malignancy, and other metabolic bone diseases.[1-4] BPs rapidly localize to hydroxyapatite in vivo and are ingested by osteoclasts, altering the resorptive function and survival of these cells.[5-7] Zoledronate (ZA; zoledronic acid), delivered intravenously, and alendronate, administered orally, are examples of more potent nitrogen-containing BPs widely used in the management of cancer and skeletal disorders, respectively.[5, 8] Mechanistically, nitrogen-containing BPs affect the mevalonate pathway by inhibiting the farnesyl diphosphate synthase, an enzyme important in the synthesis of farnesyl pyrophosphate for cholesterol biosynthesis. This prevents the prenylation of small guanosine triphosphatase (GTPase)-signaling proteins such as Rho and Ras, which are important for osteoclast regulation of the cytoskeleton, intracellular vesicular transport, and cell survival.
Although the use of BPs is beneficial for cancer and skeletal diseases treatments, BP-related osteonecrosis of the jaws (ONJ) has been reported as a serious adverse effect of these drugs.[11-13] ONJ is most frequently observed after dental interventions such as tooth extraction, in periodontal disease, and in patients receiving corticosteroid treatment.[11, 14, 15]
Despite having been described in the literature since 2004, ONJ etiology and pathophysiology remain largely unknown. Many hypotheses, including BP toxicity to oral epithelium, altered wound healing after tooth extraction, high turnover of the mandible and maxilla, oral biofilm formation, infection, and inflammation, and suppression of angiogenesis and bone turnover have been proposed.[16, 17] Since the original ONJ reports, osteoclast inhibitors with different than BP pharmacologic action have been approved for treatment of bone malignancy and osteoporosis.[18, 19] Similar ONJ incidence has been observed with these medications,[20-22] suggesting that inhibition of bone remodeling is central in the pathophysiology of the disease.
ONJ is a complex disease that involves the interaction of multiple tissues and cell types in response to local wound healing and/or infection under systemic pathologic conditions. As such, it would be difficult to replicate disease conditions in vitro. Animal models that capture several ONJ clinical, radiographic, and histologic features have been developed in rats, mice, and minipigs.[23-31] Most of these animal models involve tooth extraction in animals treated for prolonged periods with high-dose BP treatment, suggesting that BPs alter bone healing and lead to bone exposure. However, a significant fraction of ONJ diseases occurs in the absence of tooth extraction.
We recently published an animal model of ONJ using rats that have undergone experimental periodontal disease of their first and second maxillary molars and were treated with high BP doses. In these studies, no tooth extraction was performed. These findings paralleled studies in rats with diet-induced periodontitis that similarly showed ONJ-like lesions in the presence of periodontal disease and BP treatment. These studies have collectively emphasized the importance of dental disease in ONJ pathophysiology. However, because they have been performed in rats, these animal models do not explore the full range of genetic and molecular biology tools available with mice.
Here, we have developed a mouse model of ONJ, without tooth extraction, but by applying experimental periapical disease in animals treated with high BP doses. Radiographic and histologic analysis revealed quantitative and qualitative differences in the alveolar structures of vehicle (veh) versus BP-treated animals. Importantly, the mice developed osteonecrotic lesions at high frequency, which closely parallels radiographic and histologic features of ONJ in patients.
Materials and Methods
Animal care and experimental periapical disease induction
Animals and surgical procedures were handled according to guidelines of the UCLA Chancellor's Animal Research Committee. Thirty-five 4-month old C57BL/6J male mice (Jackson Laboratories, Bar Harbor, ME, USA) received intraperitoneal (IP) injections of veh (endotoxin-free water) or 200 µg/kg ZA (BP group) three times per week for 1 week prior to periapical lesion induction. The dose of 200 µg/kg is approximately threefold higher than the oncologic ZA dose of 66 µg/kg, and in the range of experimental BP doses used in other animal models.[27, 29] We chose to use this higher dose to increase the incidence of ONJ in our animals, because there appears to be a dose-dependent effect of BPs on ONJ incidence in humans.[33, 34]
Mice were anesthetized with isoflurane and mounted on a jaw retraction board. Pulpal exposure of the left first and second mandibular molars was performed utilizing a size 1/4 round bur, avoiding furcal perforation (Fig. 1A, taken at euthanasia) as described.[35, 36] Exposed teeth were left open to the oral environment. Veh or ZA IP injections continued for an additional 7 weeks, following the same protocol of 200 µg/kg ZA three times per week. We elected to inject the animals three times per week for the 8 weeks of the experiment, to mimic the monthly injections in humans given the estimation that 17 days of a rodent life correspond to 1 human year. Thus, the animals received a total of 24 ZA injections, which corresponds to 2 years of treatment for a cancer patient on IV zoledronic acid. The mean time to onset of ONJ in patients treated with ZA is approximately 18 months.
At the end of the experiment, animals were sacrificed, mandibles were removed, placed in 4% paraformaldehyde for 48 hours, and stored in 70% ethanol. Seventeen veh-treated and 18 BP-treated animals were used.
Micro–computed tomography scanning
Mouse mandibles were imaged by micro–computed tomography (µCT) scanning (µCT SkyScan 1172; SkyScan, Kontich, Belgium) at 12 µm (0.012 mm) resolution, and volumetric data were converted to Digital Imaging and Communications in Medicine (DICOM) format and imported in the Dolphin Imaging software (Chatsworth, CA, USA) to generate three-dimensional (3D) and multiplanar reconstructed images. To quantify the amount of periapical bone loss, the imaged volume was oriented so that the long axis of the distal root of the first molar (D1) was parallel to the coronal and sagittal planes. Then, the distance from the root apex to the periapical alveolar bone was measured at the distal root of the first and the mesial root of the second molars, for both the drilled and contralateral healthy sides.
To measure the width of the periodontal ligament (PDL) space and the thickness of the lamina dura at the furcation area of the first molars, a sagittal slice through the middle of the furcation area along the mesiodistal axis of the tooth was created. Three measurements at the middle of the mesial surface of the distal root, the tip of the furcation, and the middle of the distal surface of the mesial root were averaged to calculate the PDL space width and lamina dura thickness for each tooth.
To measure changes in the width of lingual bone thickness, the imaged volume was oriented such that the occlusal plane was parallel to the horizontal plane. The shortest distance from the lingual surface of the root to the lingual outline of the alveolar ridge was measured on an axial slice at the level of the apical third of the root for the distal root of the first molar and the mesial root of the second molar.
The alveolar bone, from the root apices to the alveolar crest, minus the roots and PDL space, was selected and the alveolar bone volume (BV), tissue volume (TV), and bone volume fraction (BV/TV) were measured using the CTan software (Skyscan).
Histology and tartrate-resistant acid phosphatase staining
After µCT scanning, mouse mandibular bones were decalcified in 14.5% ethylenediaminetetraacetic acid (EDTA) solution for 3 weeks. Samples were paraffin-embedded and 5-µm-thick cross sections were made perpendicular to the long axis of the alveolar ridge along the distal root of the first molar. To quantify the number of empty osteocytic lacunae, area of osteonecrosis, and periosteal thickness, hematoxylin and eosin (H&E)-stained slides were digitally scanned as described. Using the ruler tool in ImageScope (Aperio, Vista, CA, USA), the crestal 1-mm of the alveolar bone was marked. All measurements were performed in that area of the alveolar bone.
Within this area, the total number of empty and osteocytic lacunae and the osteonecrotic area(s), defined as a loss of more than five contiguous osteocytes with confluent areas of empty lacunae, were measured. Furthermore, the total bone area and perimeter were assessed. To quantify periosteal bone thickness, the ruler tool was used to measure the three greatest areas of both lingual and buccal periosteal thickness that were then averaged.
Tartrate-resistant acidic phosphatase (TRAP) positive cells were identified using the leukocyte acid phosphatase kit (Sigma-Aldrich, St. Louis, MO, USA) and counted under light microscope. All histology and digital imaging was performed at the Translational Pathology Core Laboratory (TPCL) at UCLA.
Data among groups were analyzed using one-way analysis of variance (ANOVA). Data between groups were analyzed using Student's t test.
Sagittal µCT sections through the apical area of the mandibular molars were created (Fig. 1B). In healthy teeth of veh-treated or BP-treated animals, a continuous periodontal ligament (PDL) space and uniform lamina dura were observed. In drilled teeth of veh-treated animals, widening of PDL space and loss of lamina dura, typical of periapical inflammation, were observed. Interestingly, drilled teeth in BP-treated animals showed a smaller increase in the PDL space widening and had retention of the lamina dura. A significant increase in the distance from the apex of the root to the alveolar bone (Fig. 1C) was seen on the drilled side compared to the healthy side for both veh-treated and BP-treated animals (Fig. 1D). Importantly, BP treatment resulted in significantly less periapical bone loss for drilled teeth compared to veh treatment.
Bone changes extended along the roots to the furcation area of the drilled teeth. Figure 2A shows sagittal sections through the furcation area of the first mandibular molars. In veh-treated animals healthy teeth showed a thin PDL space along the root surface (indicated by the thick arrow), and a continuous uniform lamina dura (indicated by the thin arrow). Drilled teeth of veh-treated animals showed an expansion of the PDL space and thinning of the lamina dura. Healthy teeth of BP-treated animals showed a normal PDL space. However, the lamina dura appeared thickened, compared to the healthy teeth of veh-treated animals. Significantly, in BP-treated animals, there was little widening of the PDL space and significant thickening of the lamina dura in the furcation area of drilled teeth. A statistically significant increase in PDL space and decrease in lamina dura thickness was seen in drilled teeth of veh-treated animals (Fig. 2B, C, D). BP-treatment caused a slight but statistically significant reduction in PDL space and a significant increase in lamina dura thickness in the furcation of healthy teeth. There was a small, statistically significant increase in PDL space at the furcation of drilled versus healthy teeth in BP-treated animals. However, this increase was significantly less compared to the PDL space increase in veh-treated animals. Finally, drilled teeth in BP-treated animals showed a statistically significant increase in lamina dura thickness compared to veh-treated and BP-treated healthy teeth.
The bone changes around the drilled teeth appeared to extend beyond the confines of the periodontal area to the adjacent alveolar bone (Fig. 3A). In veh-treated animals, the alveolar bone around drilled teeth showed loss of trabecular integrity and osteolysis that extended to the mandibular cortices (Fig. 3A, thick arrows). In contrast, the alveolar bone around drilled teeth of BP-treated animals showed increased trabecular density and bone deposition on the periosteal surface of the buccal and lingual cortices (Fig. 3A, thin arrows). Seventeen (94%) BP-treated animals and 1 (6%) veh-treated animal, showed periosteal bone apposition (Table 1). The shortest distance from the bone perimeter to the root surface was measured for the lingual cortex (Fig. 3B). A significant decrease in bone thickness at the drilled teeth areas in veh-treated animals was seen. BP treatment did not affect bone measurements. However, a significant increase in bone thickness was observed around drilled teeth in BP-treated animals compared to healthy teeth of either veh-treated or BP-treated animals (Fig. 3C).
|Treatment||Animals, n||Periosteal bone formation, n (%)||Histologic osteonecrosis, n (%)||Bone exposure, n (%)|
|Veh||17||1 (6%)||0 (0%)||0 (0%)|
|ZA||18||17 (94%)||16 (88%)||6 (33%)|
Then the BV, TV, and BV/TV of the alveolar ridge were measured. No difference on TV among the various groups was seen (data not shown). Dental disease did not cause any change in BV or BV/TV in the veh-treated animals. As expected, in the healthy site, BP treatment caused a significant increase of BV and BV/TV compared to veh-treated mice. Importantly, dental disease caused an even greater increase in BV and BV/TV compared to the veh-treated disease site and the healthy site of the BP-treated animals (Fig. 3D, E).
Histologic analysis showed that healthy teeth of both veh-treated and BP-treated animals had a normal PDL space and alveolar bone. Inflammatory infiltrate was observed in the apical areas of drilled teeth for both veh-treated and BP-treated animals (data not shown). Histologic examination of the periodontal molar areas revealed that healthy teeth of both veh-treated and BP-treated animals had normal periodontal structures, including marginal epithelium, crestal bone (Fig. 4A, A1, C, C1; red and aqua arrows) and periodontal ligament. Drilled teeth of both veh-treated and BP-treated animals showed inflammatory infiltrate at the gingival tissues (Fig. 4B, B1, D, D1; black arrows). Migration of marginal epithelium and reduction of the alveolar crest height was seen in the drilled teeth of veh-treated animals (Fig. 4B, B1; red and aqua arrows). Although migration of marginal epithelium was also observed in the drilled teeth of BP-treated animals (Fig. 4D, D1; red arrows) a smaller decrease in the alveolar crest height was present (Fig. 4D, D1; aqua arrows). As a result, the distance between the marginal epithelium and the alveolar crest was increased in the drilled versus healthy site of veh-treated animals, but was decreased in the drilled versus healthy site of BP-treated animals (Fig. 4B1, D1; double arrows). Finally, areas of necrotic bone characterized by empty osteocytic lacunae and periosteal bone deposition were seen in the drilled site of 16 (88%) BP-treated animals (Fig. 4D, D1; yellow and blue arrows, respectively; Table 1).
In 6 (33%) of the BP-treated animals (Table 1), histologic assessment revealed epithelial migration below the level of the alveolar crest, resulting in bone exposure (Fig. 5). At the lingual surface of the alveolar ridge, bone exposure (green arrows) and debris (red arrows), with epithelial migration (white arrows) along the necrotic bone (yellow arrow) to the level of periosteal bone deposition (blue arrows), were noted. At the buccal surface of the alveolar ridge, bone necrosis (yellow arrows) and periosteal bone deposition (blue arrows) but no bone exposure were seen. Inflammatory infiltrate (black arrows) was present throughout the alveolar ridge.
The thickness of the periosteum was measured on histologic sections at the lingual surface of the mandible. A significant increase in periosteal thickness was observed in the drilled versus healthy side of the mouse mandibles. This increased thickness, however, was more pronounced in the BP-treated versus veh-treated animals (Fig. 6A).
Then, the junctional epithelium to alveolar crest distance was measured on the lingual surface of the mandible in all animals (Fig. 6B). This distance significantly increased at the drilled site of the veh-treated animals compared to the healthy site, suggesting increased resorption of the alveolar crest. In contrast, for the BP-treated animals, a significant decrease in the junctional epithelium to alveolar crest distance was observed, probably due to the apical migration of the junctional epithelium but reduced resorption of the alveolar crest.
To quantify the effect of the various treatments on osteocytes, the number of empty osteocytic lacunae of the alveolar ridge was measured (Fig. 6C). Interestingly, increased numbers of empty osteocytic lacunae were seen in the drilled versus healthy site of veh-treated animals, suggesting that dental disease causes osteocytic death. BP treatment in the healthy site also increased the number of empty osteocytic lacunae compared to the healthy site of veh-treated animals. Importantly, the number of empty osteocytic lacunae in the drilled site of BP-treated animals was significantly higher than the healthy site of the same animals and the drilled site of veh-treated animals.
Evaluation of osteonecrotic areas (Fig. 6D) showed that osteonecrosis was present only in the drilled site of BP-treated animals, whereas no osteonecrosis was seen in any of the other groups. These areas covered on average 25.5% of the alveolar bone area and measured 176,016 ± 33,756 µm2.
We further explored whether there was a difference in empty lacunae number outside the osteonecrotic areas. We thus, made the same measurements as in Fig. 6C, instead focusing on the areas of the alveolar bone outside osteonecrosis (Fig. 7B). For the healthy and drilled site of veh-treated animals, and for the healthy site of BP-treated animals, the same numbers of empty osteocytic lacunae as in Fig. 6C were seen. Surprisingly, the number of empty lacunae for the drilled site of BP-treated animals was not different that the healthy site of the same animals or the drilled site of the veh-treated animals (Fig. 7D).
During histologic evaluation, we observed that periosteal bone deposition was present adjacent to osteonecrotic areas in the drilled site of BP-treated animals (Fig. 7A). We thus measured the percent of osteonecrotic area in a 50-µm zone next to the periosteal bone deposition (Fig. 7C). Indeed, a significantly higher osteonecrosis area was observed adjacent to periosteal bone deposits compared to the percent of osteonecrotic area for the overall alveolar bone (Fig. 7E).
Finally, TRAP assays (Fig. 8) showed a significant increase in the number of TRAP+ cells in the drilled versus healthy site for both veh-treated and BP-treated animals. However, no difference was seen in the drilled site between veh-treated and BP-treated animals (Fig. 8A). Upon closer examination, TRAP+ cells in the veh-treated animals showed close attachment to the bone with an extended contact surface. In contrast, TRAP+ cells in the BP-treated animals were round, detached, and at times removed from the bone surface (Fig. 8B).
Antiresorptive therapies are used for the management of bone diseases, including hypercalcemia of malignancy, skeletal-related events, and severe bone pain from primary or metastatic bone lesions, Paget's disease, osteoporosis, and fibrous dysplasia.[40, 41] ONJ is a serious complication of potent antiresorptive medications such as BP and denosumab, which directly affect osteoclast function and apoptosis or osteoclast formation and differentiation, respectively. Elucidating ONJ pathophysiology and developing targeted therapies is of utmost importance in the management of the disease. To this end, we have focused our efforts on developing a clinically relevant rat, and now, mouse model of ONJ to characterize objective clinical, radiographic, and histologic signs of the disease.
Caries and periodontal disease, two of the most common infectious diseases, can compromise tooth structure and support, cause inflammation of the periodontal tissues, and lead to tooth loss. In the uncompromised patient, the periapical alveolar bone or bony socket usually heal without difficulty after removal of the infectious/inflammatory insult. The coordinated osteoclastic and osteoblastic activity is central in the healing process of the involved osseous structures. However, in patients taking intravenous BPs, the risk of abnormal healing after tooth extraction is apparent.[15, 43, 44] In fact, most reported ONJ cases occur after extraction, when extractions are usually performed for periodontal disease or deep caries extending to the periapical region.[15, 43-48] The decrease in ONJ incidence after dental preventive measures further supports the role of dental disease in ONJ pathophysiology.[49, 50]
Based on these clinical observations, most animal models use tooth extractions and high-dose BP treatment, frequently in combination with dexamethasone or other chemotherapeutic agents, or metabolic deficiencies such as vitamin D deficiency, to develop ONJ-like lesions in rats, mice, or minipigs.[23, 26-31] In such models, delayed mucosal healing, ulceration, pseudoepitheliomatous hyperplasia, osteonecrosis, incomplete socket healing, and bony sequestration have been described. Interestingly, we and others have reported on ONJ animal models in rats treated with high BP doses and undergone diet-induced or ligature-induced experimental periodontitis. These animals present clinical, radiographic, and histologic features of ONJ, and recapitulate clinical ONJ in the absence of tooth extraction.[24, 25, 51] Here, we extend these studies and present a mouse ONJ model utilizing high-dose ZA and experimental periapical disease.
We used a well-established pulp exposure model of periapical disease that results in radiographically and histologically observed periapical lesions as early as 10 days after pulp exposure. In this model, osteoclastic activity is central to alveolar bone resorption, and inhibition of osteoclastic activity results in decreased size of periapical lesions.[52, 53] In agreement with these findings, we observed that the size of periapical lesions at the apices of the molar roots was significantly smaller for the BP-treated animals, as assessed by µCT imaging.
Importantly, µCT assessment of the alveolar bone revealed significant changes in bone morphology of the drilled site in BP-treated animals that closely mimicked radiographic findings in ONJ patients. Diffuse osteosclerosis with increased trabecular density, thickening of cortical outlines with periosteal bone formation that is often extensive, and thickening of the lamina dura have been described in conventional and CT radiographic examinations of ONJ patients.[54-58] and were present in the great majority (94%) of the BP-treated animals around teeth with periapical disease. Histologic findings paralleled the radiographic observations, revealing that the thickness of the periosteum that lined the buccal and lingual cortices of the alveolar ridge increased substantially in the site with periapical disease compared to the healthy side for the BP-treated animals. A more modest increase in periosteal thickness was seen in the diseased site of veh-treated animals. We made similar observations in the ONJ rat model using experimental periodontitis and high dose BP-treatment.
Histologic examination revealed the presence of diffuse loss of osteocytes and empty osteocytic lacunae denoting alveolar bone osteonecrosis, in the diseased site of 16 (88%) BP-treated animals. Interestingly, periapical disease or BP treatment alone caused a modest increase in the number of empty osteocytic lacunae that did not coalesce in osteonecrotic areas. When the number of empty osteocytic lacunae was measured in the alveolar bone outside the osteonecrotic areas, no statistical difference was detected among periapical disease, BP treatment, or the combination of dental disease with BP treatment groups, which were all higher than the veh-treated healthy group. This finding suggests that dental disease and BP treatment do not increase osteocytic death uniformly, but selectively to localized areas of the alveolar bone. Possible factors that might predispose such areas of the alveolus to osteonecrosis could include increased infection/inflammation or reduced vascularity.
Inhibition of osteoclastic activity appears to be central in ONJ pathophysiology, because clinical studies on patients treated with either BPs or denosumab, a monoclonal antibody against receptor activator of NF-κB ligand (RANKL), reveal a similar incidence of ONJ by both antiresorptive medications.[20-22] Osteoclasts with altered cell morphology, detached from the bone surface and undergoing apoptosis, are seen in ONJ patients[55, 59] on BP treatment, as well as in ONJ animal models. Similarly, we observed that although periapical disease increased TRAP+ cell numbers in both veh-treated and BP-treated mice, BP-treated animals showed round and detached TRAP+ cells.
A noteworthy observation is that 75% of the alveolar bone in a 50-µm zone adjacent to the periosteal bone deposition was necrotic, suggesting that periosteal bone deposition developed adjacent to osteonecrotic areas. It would be important to establish in future experiments whether periosteal bone reaction develops prior to osteonecrosis or vice versa. This close association of periosteal bone reaction and osteonecrosis bears clinical significance, because our findings suggest that on radiographs of ONJ patients, osteonecrosis should be suspected not only in areas of sequestration but also in areas adjacent to periosteal bone apposition.
Although most of the mice presented with histologic osteonecrosis, only 33% showed exposed bone not covered by epithelium, suggesting that bone exposure is not a prerequisite for bone necrosis. Similar observations have been reported in the rat ONJ models using experimental periodontitis,[24, 25] as well as with ONJ models using tooth extraction. These findings could have two potential implications for the clinical setting. First, in cancer patients, alveolar bone necrosis might be present around teeth with extensive periodontal or periapical disease. Extraction of such teeth would further exacerbate tissue injury and complicate healing. Second, the mice with histologic and radiographic features of ONJ but without frank bone exposure appear to resemble patients on BP treatment that present with ONJ-like radiographic or clinical symptoms but without orally exposed bone.[60-63] The original ONJ staging system has recently been changed to add stage 0 disease to include these patients.
Because our animal model did not include tooth extraction there was no experimental violation of mucosal integrity. Migration of the marginal epithelium on the diseased site of both veh-treated and BP-treated animals was observed. However, in the veh-treated animals concurrent bone resorption resulted in increased epithelial-bone crest distance. In contrast, BP-treated animals showed a significant reduction of the epithelial-bone crest distance. Importantly, in the animals with bone exposure the migrating epithelium bypassed the osteonecrotic bone to extend to the area of the vital periosteal bone apposition, thus resulting in bone exposure.
In our studies, similar to other published reports,[27, 29] we used high doses of ZA, a nitrogen-containing potent BP, to induce ONJ-like lesions in the jaws of mice that closely mimic the clinical, radiographic, and histologic features of human ONJ. These injection doses are approximately threefold higher than the ZA injection doses used in patients with bone malignancy. Although these animal models appear to capture the basic ONJ pathophysiologic mechanisms, interpretation of findings should consider the possibility of additional cell or tissue effects by the high ZA doses. Furthermore, these higher ZA doses most probably underlie the higher incidence of osteonecrosis observed in our studies, compared with published patient data.[44, 64] Future studies with pharmacologic doses similar to clinical regimens will expand use of this animal model and provide a more accurate assessment of ONJ incidence and severity.
In summary, we have created a mouse model with significant clinical, radiographic, and histologic resemblance to ONJ in patients. This model enhances existing mouse models using tooth extraction, as it addresses a subset of ONJ occurrence in the absence of traumatic interventions. Furthermore, this mouse model complements other rat ONJ models using experimental dental disease, and provides the benefits of working in a system with rich genetic and molecular tools that should assist studies of ONJ pathophysiology and targeted therapies.
ST has served as a paid consultant for and has received grant support from Amgen Inc. All other authors state that they have no conflicts of interest.
This work was supported by NIH/NIDCR DE019465 and minority supplement DE 019465-S1.
Authors' roles: All authors participated in the design, execution, and analyses of the studies. BK, SC, TA, and ST drafted the manuscript. All authors made revisions to the manuscript and approved the final version.