骨移植在预防颌骨药物相关性骨坏死中的作用:组织形态学、免疫组织化学和动物模型的临床评价。

IF 0.8 Q4 DENTISTRY, ORAL SURGERY & MEDICINE
Jonathan Ribeiro da Silva, Maria Cristina de Moraes Balbas, Caroline Águeda Corrêa, Manuella Zanela, Roberta Okamoto, Rodrigo Dos Santos Pereira, Nicolas Homsi, Eduardo Hochuli-Vieira
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引用次数: 2

摘要

目的:评价无机牛骨移植物(Lumina bone, Criteria, Brazil)和β-磷酸三钙(β-TCP)移植物(ChronOS, Synthes, Brazil)对拔牙后药物相关性颌骨坏死(MRONJ)风险大鼠的影响。方法:用唑来膦酸诱导18只体重350 ~ 450 g的雄性Wistar大鼠发生MRONJ,持续5周。第六周拔除右侧上颌第一磨牙。ⅰ组(G1)拔牙后不接受骨移植,ⅱ组(G2)接受无机牛骨移植,ⅲ组(G3)接受β-磷酸三钙(β-TCP)移植。进行临床评价、组织形态学和免疫组织化学分析。采用方差分析和Tukey统计检验,认为显著性水平为5%。结果:在临床评价中,G2和G3组动物未出现骨坏死的临床表现,而对照组(G1组)动物在所有样本中均出现坏死骨组织暴露。在组织形态学评价中,G3组骨组织形成率(66%)高于G1组(58%/32%)和G2组(59%/27%),骨陷窝形成率(18%)低于G1组(59%/27%)(P < 0.05)。G2和G3中RANKL、TRAP和OC呈中等(++)免疫染色,G1中OC呈中等(++)标记,TRAP和RANKL呈轻度(+)免疫染色。结论:β-TCP治疗小鼠骨组织形成增多,骨陷窝减少。在临床评价中,骨移植组表现出MRONJ的临床表现,TRAP和RANKL的免疫染色强度更高。尽管实验动物研究存在局限性,但这项工作的结果可能有助于未来MRONJ预防的临床研究的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Role of Bone Grafts in Preventing Medication-Related Osteonecrosis of the Jaw: Histomorphometric, Immunohistochemical, and Clinical Evaluation in Animal Model.

Objective: To evaluate the effects of inorganic bovine bone graft (Lumina Bone, Criteria, Brazil) and beta-tricalcium phosphate (β-TCP) graft (ChronOS, Synthes, Brazil) in rats with the risk of developing post-extraction medication-related osteonecrosis of the jaw (MRONJ).

Methods: Eighteen male Wistar rats weighing 350 to 450 g were induced to develop MRONJ using zoledronic acid for 5 weeks. In the sixth week, the right maxillary first molar was extracted. The animals in Group I (G1) did not receive bone grafts after tooth extraction, while Group II (G2) animals received inorganic bovine bone grafts, and Group III (G3) animals received beta-tricalcium phosphate (β-TCP) grafts. Clinical evaluation and histomorphometric and immunohistochemical analyses were performed. ANOVA and Tukey's statistical tests were used and a level of significance was considered to be 5%.

Results: In the clinical evaluation, animals from G2 and G3 did not present clinical manifestations of osteonecrosis, unlike the control group (G1) animals, which presented necrotic bone tissue exposure in all samples. In the histomorphometric evaluation, animals in G3 showed greater formation of bone tissue (66%) and less formation of bone lacuna (18%) than animals in G1 (58%/32%) and in G2 (59%/27%) (P < 0.05). Moderate (++) immunostaining was observed in G2 and G3 for RANKL, TRAP, and OC, while G1 showed moderate (++) labeling for OC and mild (+) immunostaining for TRAP and RANKL.

Conclusions: Greater formation of bone tissue and fewer bone lacunae were found in animals treated with β-TCP. In clinical evaluation, bone graft groups presented with the clinical manifestation of MRONJ and showed higher intensity of immunostaining for TRAP and RANKL. Despite the limitations of experimental animal studies, the results of this work may assist in the development of future clinical research for the prevention of MRONJ.

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Craniomaxillofacial Trauma & Reconstruction
Craniomaxillofacial Trauma & Reconstruction DENTISTRY, ORAL SURGERY & MEDICINE-
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