特殊富含序列结合蛋白 2 及其在使用合成骨移植材料和电刺激影响实验性下颌骨组织缺损填充愈合中的作用。

Q3 Medicine Polski Merkuriusz Lekarski Pub Date : 2024-01-01 DOI:10.36740/Merkur202404101
Agil N Huseynov, Vladislav A Malanchuk, Mykhailo S Myroshnychenko, Nataliia V Kapustnyk, Liliia P Sukharieva, Larisa I Selivanova
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引用次数: 0

摘要

研究目的目的:该研究的目的是确定SATB2在用合成骨移植材料和电刺激冲击填充实验性下颌骨骨组织缺损愈合中的作用:材料与方法:以 48 只成熟的雄性 WAG 大鼠为实验对象,将其分为 4 组。每组包括 12 只实验动物。第 1 组包括下颌骨穿孔模型。在动物身上,模拟骨缺损一侧的颈部区域皮下植入了一个用于电作用的微型装置。与电池负极相连的负电极与骨缺损接触。电池和电极用塑料热缩材料绝缘。第 3 组大鼠的模型与前几组相似,也有一个穿孔缺损,空腔内填充了合成骨移植材料 "Biomin GT"(乌克兰 RAPID 公司)。第 4 组的动物模型与第 1-3 组的穿孔缺损类似,腔内填充合成骨移植材料 "Biomin GT"(RAPID,乌克兰)。形态学研究的材料是从穿孔缺损区取出的下颌骨体碎片。使用兔抗人 SATB2 单克隆抗体进行免疫组化研究:结果:结果:在电刺激、用合成骨移植材料填充缺损、同时用合成骨移植材料填充缺损和电刺激的条件下,大鼠下颌骨缺损处的再生填充物中 SATB2 的表达均有所增加。在同时用合成植骨材料填充缺损和电刺激的条件下,SATB2 的表达最明显;在用合成植骨材料填充缺损的条件下,SATB2 的表达最低;在电刺激的条件下,SATB2 的表达适中。在所有治疗方法的再生组织中,免疫细胞、成纤维细胞、成骨细胞都表达了 SATB2;在电刺激条件下,脂肪细胞、血管周细胞和内皮细胞、表皮也表达了 SATB2:结论作者发现的 SATB2 表达激活是在电刺激、用合成植骨材料填充缺损、同时用合成植骨材料填充缺损和电刺激条件下刺激修复性骨生成的机制之一。
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Special at-rich sequence-binding protein 2 and its role in healing of the experimental mandible bone tissue defect filling with a synthetic bone graft material and electrical stimulation impact.

Objective: Aim: The purpose of the study was to identify the role of SATB2 in healing of the experimental mandible bone tissue defect filling with a synthetic bone graft material and electrical stimulation impact.

Patients and methods: Materials and Methods: An experiment was carried out on 48 mature male rats of the WAG population, which were divided into 4 groups. Each group included 12 experimental animals. Group 1 included rats that were modeled with a perforated defect of the lower jaw body. Group 2 included animals that were modeled with a perforated defect similar to group 1. In animals, a microdevice for electrical action was implanted subcutaneously in the neck area on the side of the simulated bone defect. The negative electrode connected to the negative pole of the battery was in contact with the bone defect. The battery and electrode were insulated with plastic heat shrink material. Group 3 included rats that were modeled with a perforated defect similar to previous groups, the cavity of which was filled with synthetic bone graft "Biomin GT" (RAPID, Ukraine). Group 4 included animals that were modeled with a perforated defect similar to groups 1-3, the cavity of which was filled with synthetic bone graft "Biomin GT" (RAPID, Ukraine). The simulation of electrical stimulation was the same as in group 2. The material for the morphological study was a fragment of the body of the lower jaw from the zone of the perforated defect. Immunohistochemical study was performed using rabbit anti-human SATB2 monoclonal antibody.

Results: Results: In the regenerate filling the defect in the bone tissue of the lower jaw of rats, there was an increase in SATB2 expression under conditions of electrical stimulation; filling the defect with a synthetic bone graft material; simultaneous filling the defect with a synthetic bone graft material and electrical stimulation. The most pronounced expression of SATB2 was observed under conditions of simultaneous filling the defect with a synthetic bone graft material and electrical stimulation; minimally expressed - in conditions of filling the defect with a synthetic bone graft material; moderately expressed - under conditions of electrical stimulation. In the regenerate, in cases of all treatment methods, SATB2 was expressed by immune cells, fibroblastic differon cells, osteoblasts, and in case of electrical stimulation, also by adipocytes, vascular pericytes and endothelial cells, epidermis.

Conclusion: Conclusions: The activation of SATB2 expression identified by the authors is one of the mechanisms for stimulating reparative osteogenesis under the conditions of electrical stimulation; filling the defect with a synthetic bone graft material; simultaneous filling the defect with a synthetic bone graft material and electrical stimulation.

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Polski Merkuriusz Lekarski
Polski Merkuriusz Lekarski Medicine-Medicine (all)
CiteScore
1.90
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0.00%
发文量
84
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