The Microdamage and Expression of Sclerostin in Peri-implant Bone under One-time Shock Force Generated by Impact

• Published in: Scientific reports 2017-07, Vol.7 (1), p.6508-10, Article 6508
• Main Authors: Diao, Xiaoou, Li, Zhirui, An, Baili, Xin, Haitao, Wu, Yulu, Li, Kai, Feng, Fan, Dou, Chenyun
• Format: Article
• Language: English
• Subjects: 13; 14/19; 38/35; 38/77; 692/308/1426; 692/700/806; Animals; beta Catenin - biosynthesis; Bone growth; Bone implants; Bone Morphogenetic Proteins - biosynthesis; Bone Remodeling; Bone resorption; Computed tomography; Fractures; Gene Expression Profiling; Histocytochemistry; Histology; Humanities and Social Sciences; Immunofluorescence; Immunohistochemistry; Mechanical loading; multidisciplinary; Osseointegration; Ossicular Replacement; Osteogenesis; Rabbits; RANK Ligand - biosynthesis; Real-Time Polymerase Chain Reaction; Science; Science (multidisciplinary); SOST protein; Stress, Mechanical; Time Factors; TRANCE protein; Transplants & implants; Wnt protein; X-Ray Microtomography; β-Catenin
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-017-06867-9

Osseointegration is the key to implant stability and occlusal support. Biomechanical response and remodeling of peri-implant bone occurs under impact loading. Sclerostin participates in bone formation and resorption through Wnt and RANKL pathways. However the mechanism of microdamage and expression of sclerostin in peri-implant bone under impact load is still unclear. In present study, specific impact forces were applied to the implants with favorable osseointegration in rabbits. The microdamage of peri-implant bone and the expression of sclerostin, β-catenin and RANKL during the process of bone damage and remodeling were investigated by micro-CT, histology, immunofluorescence and RT-qPCR analysis. Interface separation and trabecular fracture were found histologically, which were consistent with micro-CT analyses. Throughout remodeling, bone resorption was observed during the first 14 days after impact, and osseointegration and normal trabecular structure were found by 28 d. The expression of sclerostin and RANKL increased after impact and reached a maximum by 14 d, then decreased gradually to normal levels by 28 d. And β-catenin expression was opposite. Results indicated that sclerostin may involve in the peri-implant bone damage caused by impact and remodeling through Wnt/β-catenin and RANKL/RANK pathways. It will provide a new insight in the diagnosis and treatment for patients suffering impact.