Ohtsu A, Kusakari H, Maeda T, Takano Y
Department of Prosthetic Dentistry, Niigata University School of Dentistry, Japan.
J Periodontol. 1997 Mar;68(3):270-83. doi: 10.1902/jop.1997.68.3.270.
Implant materials are placed under various sites-including cortical bone, spongy bone, and bone marrow-at the same time according to the depth at implantation. Although cortical bone is an important site for the prognosis of implantation, detailed reports on tissue responses to implantation have been meager. The present study aims to reveal tissue responses to pure titanium implantation in rat femoris cortical bone. The rats received titanium bars surgically in their femurs and were sacrificed 1 day to 40 weeks post-implantation. The prepared tissue specimens were processed for light and transmission electron microscopy (TEM). Further histochemical detections were performed. One day post-implantation, empty osteocytic lacunae indicating degeneration of osteocytes were found in pre-existing cortical bone around the implant. Such pre-existing bone was replaced by new bone, but remained in part even 40 weeks post-implantation. Light microscopy showed that direct contact between the implant and new bone was identified 12 weeks post-implantation. Chronological and ultrastructural observation showed that new bone deposition appeared to proceed toward the implant, and that the intervening layer at the interface was derived from the degenerated debris of multinucleated giant cells and/or osteoblasts. Furthermore, it seemed that the width of intervening layer varied in relation to the distance from the blood vessels. The cells showing tartrate resistant acid phosphatase activity possessed cytological features of osteoclasts under TEM; they were frequently observed in perivascular sites near the implants even after osseointegration, suggesting that bone remodeling took place steadily around the implant.
根据植入深度,同时将植入材料放置在包括皮质骨、松质骨和骨髓在内的不同部位。尽管皮质骨是植入预后的重要部位,但关于植入组织反应的详细报道却很少。本研究旨在揭示大鼠股骨皮质骨中纯钛植入后的组织反应。大鼠通过手术在股骨中植入钛棒,并在植入后1天至40周处死。制备的组织标本进行光镜和透射电镜(TEM)处理。进一步进行组织化学检测。植入后1天,在植入物周围预先存在的皮质骨中发现空的骨陷窝,表明骨细胞发生退变。这种预先存在的骨被新骨取代,但即使在植入后40周仍部分保留。光镜显示,植入后12周可识别植入物与新骨之间的直接接触。时间顺序和超微结构观察表明,新骨沉积似乎朝着植入物方向进行,界面处的中间层来源于多核巨细胞和/或成骨细胞的退变碎片。此外,中间层的宽度似乎与距血管的距离有关。在透射电镜下,显示抗酒石酸酸性磷酸酶活性的细胞具有破骨细胞的细胞学特征;即使在骨整合后,它们也经常在植入物附近的血管周围部位观察到,表明植入物周围的骨重塑稳定发生。