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Bone marrow coagulated and low‐level laser therapy accelerate bone healing by enhancing angiogenesis, cell proliferation, osteoblast differentiation, and mineralization
Journal of Biomedical Materials Research Part A ( IF 4.9 ) Pub Date : 2020-08-09 , DOI: 10.1002/jbm.a.37076
Carolina S Santinoni 1, 2 , Adrieli P C Neves 1, 2 , Breno F M Almeida 3 , Natália C Kajimoto 2 , Natália M Pola 4 , Eliana A Caliente 2 , Eduarda L G Belem 2 , Joilson B Lelis 2 , Stephen E Fucini 2, 5 , Michel R Messora 6 , Valdir G Garcia 2 , Suely R M Bomfim 3 , Edilson Ervolino 7 , Maria J H Nagata 2
Affiliation  

The present study evaluated bone marrow aspirate (BMA) and low‐level laser therapy (LLLT) on bone healing. It was created critical‐size defects (CSD) of 5 mm diameter in rat calvaria of 64 rats. Animals were randomly divided into four groups: Control (blood clot), BMA (coagulated BMA), LLLT (laser irradiation and blood clot), and BMA/LLLT (laser irradiation and coagulated BMA). Euthanasia was performed at 15 or 30 days postoperative. Immunohistochemical reactions were performed to identify vascular endothelial growth factor (VEGF), proliferating cell nuclear antigen (PCNA), runt‐related transcription factor‐2 (Runx2), bone morphogenetic protein‐2 (BMP‐2), osteocalcin (OCN), and osteopontin (OPN). The markers were quantified, and data were statistically analyzed. Groups BMA/LLLT and LLLT presented significantly higher VEGF expression than group control. Group BMA/LLLT presented a significantly higher expression of PCNA than all experimental groups. Groups BMA and BMA/LLLT presented significantly higher expression of BMP‐2 than all experimental groups. Groups LLLT and BMA/LLLT presented significantly higher expression of OPN than groups control and BMA. Groups LLLT, BMA, and BMA/LLLT presented a significantly higher expression of OCN than group control. It can be concluded that the association of BMA and LLLT enhanced bone healing by improving expression of VEGF, PCNA, Runx2, BMP‐2, OPN, and OCN.

中文翻译:

骨髓凝固和低强度激光治疗通过增强血管生成、细胞增殖、成骨细胞分化和矿化加速骨愈合

本研究评估了骨髓穿刺(BMA)和低强度激光治疗(LLLT)对骨愈合的影响。它在 64 只大鼠的大鼠颅骨中产生了直径为 5 毫米的临界尺寸缺陷 (CSD)。将动物随机分为四组:对照(血凝块)、BMA(凝固的 BMA)、LLLT(激光照射和血凝块)和 BMA/LLLT(激光照射和凝固的 BMA)。安乐死在术后 15 或 30 天进行。进行免疫组织化学反应以鉴定血管内皮生长因子 (VEGF)、增殖细胞核抗原 (PCNA)、矮小相关转录因子 2 (Runx2)、骨形态发生蛋白 2 (BMP-2)、骨钙素 (OCN) 和骨桥蛋白(OPN)。对标记物进行量化,并对数据进行统计分析。BMA/LLLT 和 LLLT 组的 VEGF 表达显着高于对照组。BMA/LLLT 组的 PCNA 表达明显高于所有实验组。BMA 和 BMA/LLLT 组的 BMP-2 表达显着高于所有实验组。LLLT 和 BMA/LLLT 组的 OPN 表达显着高于对照组和 BMA。LLLT、BMA 和 BMA/LLLT 组的 OCN 表达显着高于对照组。可以得出结论,BMA 和 LLLT 的联合通过提高 VEGF、PCNA、Runx2、BMP-2、OPN 和 OCN 的表达来促进骨愈合。LLLT 和 BMA/LLLT 组的 OPN 表达显着高于对照组和 BMA。LLLT、BMA 和 BMA/LLLT 组的 OCN 表达显着高于对照组。可以得出结论,BMA 和 LLLT 的联合通过提高 VEGF、PCNA、Runx2、BMP-2、OPN 和 OCN 的表达来促进骨愈合。LLLT 和 BMA/LLLT 组的 OPN 表达显着高于对照组和 BMA。LLLT、BMA 和 BMA/LLLT 组的 OCN 表达显着高于对照组。可以得出结论,BMA 和 LLLT 的联合通过提高 VEGF、PCNA、Runx2、BMP-2、OPN 和 OCN 的表达来促进骨愈合。
更新日期:2020-08-09
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