表皮生长因子、硼酸及其复方制剂对大鼠软骨损伤的疗效调查:实验研究。

IF 1.9 Q2 ORTHOPEDICS Joint diseases and related surgery Pub Date : 2024-01-01 Epub Date: 2023-11-30 DOI:10.52312/jdrs.2023.1074
Bilge Kağan Yılmaz, Mehmet Nuri Konya, Sinan İnce, Hasan Hüseyin Demirel, Yüksel Çetin, Ayşen Güngör
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引用次数: 0

摘要

研究目的本研究旨在确定表皮生长因子(EGF)、硼酸(BA)及其组合对大鼠软骨损伤的生物效应:在体外环境中,使用小鼠成纤维细胞(L929)、人骨肉瘤细胞(Saos-2)和人脂肪间充质干细胞(hAD-MSCs),通过 MTT [3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氮唑] 试验确定硼酸、表皮生长因子及其组合的细胞毒性作用。在体内环境中,72 只大鼠被随机分为四组。各组均创建标准软骨缺损并进行微骨折。A 组为对照组。除标准程序外,B 组接受 100 ng/mL 的 EGF,C 组接受 100 ng/mL 的 EGF 和 10 µg/mL 的 BA 组合,D 组接受 20 µg/mL 的 BA:结果:EGF 稀释液(1、5、10、25、50、100、200 ng/mL)与 BA(100、300、500 µg/mL)的组合仅在 72 小时应用期和 Saos-2 中观察到细胞毒性作用。BA 与 EGF 合用时,其细胞毒性作用减弱。各组组织病理学评分无明显差异(P=0.13):我们的研究表明,应用 EGF 和低剂量 BA 对大鼠软骨愈合有积极作用。结论:我们的研究表明,应用 EGF 和低剂量 BA 对大鼠软骨愈合有积极作用。EGF 和 BA 的联合应用促进了成骨细胞的生长。在使用 20 µg/mL BA 的组别中发现了溶解性病变,这表明 BA 可能具有细胞毒性作用。
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Investigation of the efficacy of epidermal growth factor, boric acid and their combination in cartilage injury in rats: An experimental study.

Objectives: In this study, we aimed to determine the bioefficacy of epidermal growth factor (EGF), boric acid (BA), and their combination on cartilage injury in rats.

Materials and methods: In in vitro setting, the cytotoxic effects of BA, EGF, and their combinations using mouse fibroblast cell (L929), human bone osteosarcoma cell (Saos-2), and human adipose derived mesenchymal stem cells (hAD-MSCs) were determined by applying MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide] test. In in vivo setting, 72 rats were randomly divided into four groups. A standard chondral defect was created and microfracture was performed in all groups. Group A was determined as the control group. In addition to the standard procedure, Group B received 100 ng/mL of EGF, Group C received a combination of 100 ng/mL of EGF and 10 µg/mL of BA combination, and Group D 20 µg/mL of BA.

Results: The cytotoxic effect of the combinations of EGF dilutions (1, 5, 10, 25, 50, 100, 200 ng/mL) with BA (100, 300, 500 µg/mL) was observed only in the 72-h application period and in Saos-2. The cytotoxic effect of BA was reduced when combined with EGF. There was no significant difference in the histopathological scores among the groups (p=0.13).

Conclusion: Our study showed that EGF and low-dose BA application had a positive effect on cartilage healing in rats. Significant decreases in recovery scores were observed in the other groups. The combination of EGF and BA promoted osteoblast growth. Detection of lytic lesions in the group treated with 20 µg/mL of BA indicates that BA may have a cytotoxic effect.

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