Suppr超能文献

正畸诱导的牙周膜损伤的扫描电子显微镜研究

Scanning electron microscopic study of orthodontically induced injuries to the periodontal membrane.

作者信息

Lindskog S, Lilja E

出版信息

Scand J Dent Res. 1984 Aug;92(4):334-43. doi: 10.1111/j.1600-0722.1984.tb00900.x.

Abstract

Scanning electron microscopy was used to study vascular and cellular changes in the periodontal membrane (PDM) in rats after orthodontic treatment ranging from 3 h to 9 days. The orthodontic forces ranged between 200 mN and 400 mN. Within the first hours of treatment extravasated erythrocytes, eichinocytes and platelets in various stages of degeneration were found in the pressure zones. The connective tissue of the pressure zones developed an amorphous appearance lacking discernible fibers and blood vessels following treatment for 24 h. These areas are known as hyaline zones, an area of local aseptic necorsis. Three days after the application of an orthodontic force macrophage-like cells were abundant close to the hyaline zone. They adhered to the hyaline zone with filopods radiating from pseudopods. Large osteoclast-like cells with several projections towards the bone surface were found around the hyaline zone and in the marrow spaces close to the pressure zones. The results indicated that the tissue reactions leading to remodeling of the PDM in the pressure zones are closely related to vascular injuries and subsequent formation of coagulated blood. Furthermore, macrophages seem to be the cells which play the most important role during degradation of the hyaline zone.

摘要

利用扫描电子显微镜研究了正畸治疗3小时至9天后大鼠牙周膜(PDM)中的血管和细胞变化。正畸力在200毫牛至400毫牛之间。在治疗的最初几个小时内,在压力区发现了外渗的红细胞、棘形细胞和处于不同退变阶段的血小板。治疗24小时后,压力区的结缔组织呈现出无定形外观,缺乏可辨认的纤维和血管。这些区域被称为透明带,即局部无菌性坏死区域。施加正畸力三天后,类似巨噬细胞的细胞在透明带附近大量存在。它们通过从伪足放射出的丝状伪足附着在透明带上。在透明带周围以及靠近压力区的骨髓腔中发现了具有多个朝向骨表面突起的大型破骨细胞样细胞。结果表明,导致压力区牙周膜重塑的组织反应与血管损伤及随后形成的凝血密切相关。此外,巨噬细胞似乎是在透明带降解过程中起最重要作用的细胞。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验