Miyamoto Y, Hayashi H, Kamoi K
Nihon Shishubyo Gakkai Kaishi. 1989 Dec;31(4):1047-59. doi: 10.2329/perio.31.1047.
The aim of this study is to determine the process of periodontal tissue regeneration and the metabolic activity of osteoblasts after implantation of bone ceramic and collagen gel compound materials (BC). Bone defects were artificially prepared in the alveolar septa of the bilateral upper first and second molars of Wistar rats. Subsequently, BC were implanted into the defective sites on the left side, and the gingival flaps were closed. At the defective sites on the right side, as a control, gingival flaps were closed without implantation. Rats were sacrificed 1, 3, 5, 7 or 14 weeks after implantation, and prepared tissue sections were observed both pathologically and autoradiographically using 3H-Proline. The results obtained were as follows: Pathological Findings One week after BC implantation, inflammatory cellular infiltration of the surrounding gingival connective tissue was relatively mild. Three weeks after implantation, BC were present in fibrous connective tissues, and some directly bound to the marices of regenerated bone. Observation 5 weeks after implantation revealed that BC had become embedded in the regenerated bone matrices and that there was giant cell reaction to foreign bodies at the margin of BC located in connective tissue. BC were directly bound to the regenerated bone matrices without intermediary fibrous tissues 7 and 14 weeks after implantation. Connective tissues showed high grade regeneration of collagen fiber bundles, in an arrangement that tended to be fixed in mesial and distal directions. Autoradiographic Findings There was no uptake of 3H-Proline into the regenerated bone matrices or the gingival connective tissue surrounding BC, while uptake of 3H-Proline into the entire area around the root apex and in the vicinity of the alveolar septum was observed with time (weeks) after BC implantation. These results suggest that BC provide nuclei for bone regeneration through inclusion in newly-generated periodontal bone tissue, although it is difficult to produce definite induction of bone tissue by BC alone. It is also apparent that these are useful bone implantation materials for restoration of the physiological morphology of alveolar bone in periodontal surgical treatment.
本研究旨在确定骨陶瓷与胶原凝胶复合材料(BC)植入后牙周组织再生过程及成骨细胞的代谢活性。在Wistar大鼠双侧上颌第一和第二磨牙的牙槽间隔处人工制备骨缺损。随后,将BC植入左侧缺损部位,并关闭牙龈瓣。右侧缺损部位作为对照,不植入材料直接关闭牙龈瓣。植入后1、3、5、7或14周处死大鼠,制备组织切片,采用3H-脯氨酸进行病理和放射自显影观察。结果如下:病理结果:BC植入后1周,周围牙龈结缔组织的炎性细胞浸润相对较轻。植入后3周,BC存在于纤维结缔组织中,部分直接与再生骨的基质结合。植入后5周观察发现,BC已嵌入再生骨基质中,位于结缔组织中的BC边缘有异物巨细胞反应。植入后7周和14周,BC直接与再生骨基质结合,无中间纤维组织。结缔组织显示胶原纤维束高度再生,排列倾向于沿近中和远中方向固定。放射自显影结果:3H-脯氨酸未被摄取到再生骨基质或BC周围的牙龈结缔组织中,而在BC植入后的不同时间(周)观察到3H-脯氨酸被摄取到根尖周围的整个区域和牙槽间隔附近。这些结果表明,BC通过融入新生成的牙周骨组织为骨再生提供核心,尽管仅靠BC难以产生明确的骨组织诱导作用。显然,这些是牙周手术治疗中用于恢复牙槽骨生理形态的有用骨植入材料。