<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(1)</volume><submitter>Diao X</submitter><pubmed_abstract>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 consisten</pubmed_abstract><journal>Scientific reports</journal><pagination>6508</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5529451</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The Microdamage and Expression of Sclerostin in Peri-implant Bone under One-time Shock Force Generated by Impact.</pubmed_title><pmcid>PMC5529451</pmcid><pubmed_authors>An B</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Diao X</pubmed_authors><pubmed_authors>Feng F</pubmed_authors><pubmed_authors>Xin H</pubmed_authors><pubmed_authors>Li K</pubmed_authors><pubmed_authors>Wu Y</pubmed_authors><pubmed_authors>Dou C</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Microdamage and Expression of Sclerostin in Peri-implant Bone under One-time Shock Force Generated by Impact.</name><description>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 consisten</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Jul</publication><modification>2025-04-04T12:50:06.37Z</modification><creation>2019-03-27T02:51:47Z</creation></dates><accession>S-EPMC5529451</accession><cross_references><pubmed>28747741</pubmed><doi>10.1038/s41598-017-06867-9</doi></cross_references></HashMap>