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Osteocytic Sclerostin Expression in Alveolar Bone in Rats With Diabetes Mellitus and Ligature-Induced Periodontitis

DC Field Value Language
dc.contributor.author박은정-
dc.contributor.author유윤정-
dc.contributor.author이동은-
dc.contributor.author차정헌-
dc.date.accessioned2016-02-04T11:40:43Z-
dc.date.available2016-02-04T11:40:43Z-
dc.date.issued2015-
dc.identifier.issn0022-3492-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/140955-
dc.description.abstractBACKGROUND: Osteocytic sclerostin inhibits bone formation, and its expression is stimulated by tumor necrosis factor (TNF)-α. This study investigates sclerostin and TNF-α expression in rats with diabetes mellitus (DM) and periodontitis. METHODS: Rats were divided into control (C), periodontitis (P), and DM + periodontitis (DP) groups. After induction of DM by streptozotocin, periodontitis was induced by ligature. At day 0 (control) and at days 3 and 20 after induction of periodontitis, alveolar bone, osteoclasts, osteoid area, and TNF-α and sclerostin expression were evaluated. RESULTS: The distance between the cemento-enamel junction and the alveolar bone crest of the DP group was longer than that of the P group at day 20 after induction of periodontitis, but the number of osteoclasts was not different. Osteoid area decreased in both the P and DP groups by day 3, but whereas sustained osteoid suppression was observed in the DP group at day 20, osteoid formation was increased in the P group. The number of sclerostin-positive osteocytes increased in both groups at day 3, but the increased number of sclerostin-positive osteocytes was maintained only in the DP group through day 20. The number of TNF-α-positive cells increased more in the DP group than in the P group. CONCLUSIONS: Enhanced alveolar bone loss, suppressed bone formation, and prevalent TNF-α expression were characteristic of the DP group compared with the P group. Suppressed bone formation in the DP group was observed simultaneously with increased sclerostin and TNF-α expression. These results suggest that upregulated osteocytic sclerostin expression in periodontitis accompanied by DM may play a role in suppressed bone formation.-
dc.description.statementOfResponsibilityopen-
dc.format.extent1005~1011-
dc.relation.isPartOfJOURNAL OF PERIODONTOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAlveolar Bone Loss/metabolism-
dc.subject.MESHAlveolar Bone Loss/pathology-
dc.subject.MESHAlveolar Process/chemistry*-
dc.subject.MESHAnimals-
dc.subject.MESHBone Matrix/chemistry-
dc.subject.MESHBone Morphogenetic Proteins/analysis*-
dc.subject.MESHDiabetes Mellitus, Experimental/metabolism*-
dc.subject.MESHGenetic Markers-
dc.subject.MESHInterleukin-1beta/analysis-
dc.subject.MESHMale-
dc.subject.MESHOsteoclasts/chemistry-
dc.subject.MESHOsteoclasts/pathology-
dc.subject.MESHOsteocytes/chemistry*-
dc.subject.MESHOsteocytes/pathology-
dc.subject.MESHOsteogenesis/physiology-
dc.subject.MESHPeriodontitis/metabolism*-
dc.subject.MESHRats-
dc.subject.MESHRats, Inbred F344-
dc.subject.MESHStreptozocin-
dc.subject.MESHTime Factors-
dc.subject.MESHTooth Cervix/pathology-
dc.subject.MESHTumor Necrosis Factor-alpha/analysis-
dc.titleOsteocytic Sclerostin Expression in Alveolar Bone in Rats With Diabetes Mellitus and Ligature-Induced Periodontitis-
dc.typeArticle-
dc.contributor.collegeResearcher Institutes (부설 연구소)-
dc.contributor.departmentOral Cancer Research Institute (구강종양연구소)-
dc.contributor.googleauthorJi Hye Kim-
dc.contributor.googleauthorDong Eun Lee-
dc.contributor.googleauthorGye Hyeong Woo-
dc.contributor.googleauthorJeong Heon Cha-
dc.contributor.googleauthorEun Jung Bak-
dc.contributor.googleauthorYun Jung Yoo-
dc.identifier.doi10.1902/jop.2015.150083-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA01614-
dc.contributor.localIdA02490-
dc.contributor.localIdA02730-
dc.contributor.localIdA04007-
dc.relation.journalcodeJ01697-
dc.identifier.eissn1943-3670-
dc.identifier.pmid25855571-
dc.identifier.urlhttp://www.joponline.org/doi/abs/10.1902/jop.2015.150083-
dc.subject.keywordBone morphogenetic proteins-
dc.subject.keyworddiabetes mellitus-
dc.subject.keywordosteogenesis-
dc.subject.keywordperiodontitis-
dc.subject.keywordsclerostin protein, rat-
dc.subject.keywordtumor necrosis factor-α-
dc.contributor.alternativeNameBak, Eun-Jung-
dc.contributor.alternativeNameYoo, Yun Jung-
dc.contributor.alternativeNameLee, Dong Eun-
dc.contributor.alternativeNameCha, Jung Heon-
dc.contributor.affiliatedAuthorBak, Eun-Jung-
dc.contributor.affiliatedAuthorYoo, Yun Jung-
dc.contributor.affiliatedAuthorLee, Dong Eun-
dc.contributor.affiliatedAuthorCha, Jung Heon-
dc.rights.accessRightsnot free-
dc.citation.volume86-
dc.citation.number8-
dc.citation.startPage1005-
dc.citation.endPage1011-
dc.identifier.bibliographicCitationJOURNAL OF PERIODONTOLOGY, Vol.86(8) : 1005-1011, 2015-
dc.identifier.rimsid30416-
dc.type.rimsART-
Appears in Collections:
2. College of Dentistry (치과대학) > Research Institute (부설연구소) > 1. Journal Papers
2. College of Dentistry (치과대학) > Dept. of Oral Biology (구강생물학교실) > 1. Journal Papers

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