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Influence of heat stress to matrix on bone formation

化学 标记法 骨桥蛋白 碱性磷酸酶 骨愈合 酸性磷酸酶 H&E染色 类骨质 免疫组织化学 热休克蛋白 病理 细胞凋亡 生物物理学 解剖 内科学 医学 生物 生物化学 基因
作者
Keiko Yoshida,Katsumi Uoshima,Kimimitsu Oda,Takeyasu Maeda
出处
期刊:Clinical Oral Implants Research [Wiley]
卷期号:20 (8): 782-790 被引量:58
标识
DOI:10.1111/j.1600-0501.2009.01654.x
摘要

Abstract Objectives: It is important to know the etiology of implant failure. It has been reported that heat stress during drilling was one of the causes for failure and the threshold was 47°C. However, clinically, we encounter cases in which overheating does not seem to affect osseointegration eventually. The purpose of this study was to assess histologically the spatio‐temporal effect of heat stress on bone formation after overheating the bone matrix. Material and methods: Rat calvarial bone was heated to 37°C, 43°C, 45°C and 48°C for 15 min by a temperature stimulator. Paraffin sections were prepared 1, 3 and 5 weeks after heating and investigated histologically under light microscopy. Hematoxylin and eosin staining, alkaline phosphatase (ALP), osteopontin (OPN), heat shock protein 27 (Hsp27) and heat shock protein 70 (Hsp70) immunohistochemistry and tartrate‐resistant acid phosphatase (TRAP) enzyme histochemistry were carried out. The area of dead osteocytes was calculated and statistically analyzed. Apoptotic osteocytes were detected by the terminal deoxynucleotidyltransferase‐mediated dUTP nick end‐labeling (TUNEL) method. Results: Along with the temperature increase, the area of dead osteocytes increased and regeneration of the periosteal membrane was delayed. Hsps‐ and TUNEL‐positive cells were only seen in the 48°C group. Spatio‐temporal changes of TRAP‐ and ALP‐positive cell numbers were observed, while OPN expression was mostly absent. Even after 48°C stimulation, bone formation on the calvarial surface was observed after 5 weeks. Conclusions: Although there was a temperature‐dependent delay in bone formation after heat stress, the 48°C heat stress did not obstruct bone formation eventually. This delay was probably caused by slow periosteal membrane regeneration.
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