Rodents as an animal model for studying tooth extraction-related medication-related osteonecrosis of the jaw: assessment of outcomes

被引:6
|
作者
Hadad, Henrique [1 ,2 ]
Matheus, Henrique R. [1 ,3 ]
Pai, Sara I. [4 ]
Souza, Francisley A. [2 ]
Guastaldi, Fernando P. S. [1 ,5 ]
机构
[1] Harvard Sch Dent Med, Massachusetts Gen Hosp, Dept Oral & Maxillofacial Surg, Boston, MA USA
[2] Sao Paulo State Univ UNESP, Sch Dent, Dept Diag & Surg, Oral & Maxillofacial Surg Div, Aracatuba, SP, Brazil
[3] Sao Paulo State Univ UNESP, Sch Dent, Dept Diag & Surg, Periodont Div, Aracatuba, SP, Brazil
[4] Yale Univ, Sch Med, Dept Surg, Div Otolaryngol Head & Neck Surg, New Haven, CT USA
[5] Harvard Sch Dent Med, Massachusetts Gen Hosp, Skeletal Biol Res Ctr, Dept Oral & Maxillofacial Surg, 50 Blossom St,Thier Res Bldg,513A, Boston, MA 02114 USA
关键词
MRONJ; ONJ; BRONJ; Bisphosphonates; Antiresorptive; BISPHOSPHONATE-RELATED OSTEONECROSIS; ZOLEDRONIC ACID; DENTAL EXTRACTIONS; STEM-CELLS; RAT MODEL; BONE; ALENDRONATE; LESIONS; MICE; THERAPY;
D O I
10.1016/j.archoralbio.2023.105875
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective: To assess the outcomes of several rodent animal models for studying tooth extraction-related medication-related osteonecrosis of the jaw (MRONJ). Design: After a search of the databases, 2004 articles were located, and 118 corroborated the inclusion factors (in vivo studies in rodents evaluating tooth extraction as a risk factor for the development of MRONJ). Results: Numerous studies attempting to establish an optimal protocol to induce MRONJ were found. Zoledronic acid (ZA) was the most used drug, followed by alendronate (ALN). Even when ZA did not lead to the development of MRONJ, its effect compromised the homeostasis of the bone and soft tissue. The association of other risk factors (dexamethasone, diabetes, and tooth-related inflammatory dental disease) besides tooth extraction also played a role in the development of MRONJ. In addition, studies demonstrated a relationship between cumulative dose and MRONJ. Conclusions: Both ZA and ALN can lead to MRONJ in rodents when equivalent human doses (in osteoporosis or cancer treatment) are used. Local oral risk factors and tooth-related inflammatory dental disease increase the incidence of MRONJ in a tooth extraction-related rodent model.
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页数:19
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