Cited 25 times in
Osteocytic Sclerostin Expression in Alveolar Bone in Rats With Diabetes Mellitus and Ligature-Induced Periodontitis
DC Field | Value | Language |
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dc.contributor.author | 박은정 | - |
dc.contributor.author | 유윤정 | - |
dc.contributor.author | 이동은 | - |
dc.contributor.author | 차정헌 | - |
dc.date.accessioned | 2016-02-04T11:40:43Z | - |
dc.date.available | 2016-02-04T11:40:43Z | - |
dc.date.issued | 2015 | - |
dc.identifier.issn | 0022-3492 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/140955 | - |
dc.description.abstract | BACKGROUND: 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.statementOfResponsibility | open | - |
dc.format.extent | 1005~1011 | - |
dc.relation.isPartOf | JOURNAL OF PERIODONTOLOGY | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Alveolar Bone Loss/metabolism | - |
dc.subject.MESH | Alveolar Bone Loss/pathology | - |
dc.subject.MESH | Alveolar Process/chemistry* | - |
dc.subject.MESH | Animals | - |
dc.subject.MESH | Bone Matrix/chemistry | - |
dc.subject.MESH | Bone Morphogenetic Proteins/analysis* | - |
dc.subject.MESH | Diabetes Mellitus, Experimental/metabolism* | - |
dc.subject.MESH | Genetic Markers | - |
dc.subject.MESH | Interleukin-1beta/analysis | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Osteoclasts/chemistry | - |
dc.subject.MESH | Osteoclasts/pathology | - |
dc.subject.MESH | Osteocytes/chemistry* | - |
dc.subject.MESH | Osteocytes/pathology | - |
dc.subject.MESH | Osteogenesis/physiology | - |
dc.subject.MESH | Periodontitis/metabolism* | - |
dc.subject.MESH | Rats | - |
dc.subject.MESH | Rats, Inbred F344 | - |
dc.subject.MESH | Streptozocin | - |
dc.subject.MESH | Time Factors | - |
dc.subject.MESH | Tooth Cervix/pathology | - |
dc.subject.MESH | Tumor Necrosis Factor-alpha/analysis | - |
dc.title | Osteocytic Sclerostin Expression in Alveolar Bone in Rats With Diabetes Mellitus and Ligature-Induced Periodontitis | - |
dc.type | Article | - |
dc.contributor.college | Researcher Institutes (부설 연구소) | - |
dc.contributor.department | Oral Cancer Research Institute (구강종양연구소) | - |
dc.contributor.googleauthor | Ji Hye Kim | - |
dc.contributor.googleauthor | Dong Eun Lee | - |
dc.contributor.googleauthor | Gye Hyeong Woo | - |
dc.contributor.googleauthor | Jeong Heon Cha | - |
dc.contributor.googleauthor | Eun Jung Bak | - |
dc.contributor.googleauthor | Yun Jung Yoo | - |
dc.identifier.doi | 10.1902/jop.2015.150083 | - |
dc.admin.author | false | - |
dc.admin.mapping | false | - |
dc.contributor.localId | A01614 | - |
dc.contributor.localId | A02490 | - |
dc.contributor.localId | A02730 | - |
dc.contributor.localId | A04007 | - |
dc.relation.journalcode | J01697 | - |
dc.identifier.eissn | 1943-3670 | - |
dc.identifier.pmid | 25855571 | - |
dc.identifier.url | http://www.joponline.org/doi/abs/10.1902/jop.2015.150083 | - |
dc.subject.keyword | Bone morphogenetic proteins | - |
dc.subject.keyword | diabetes mellitus | - |
dc.subject.keyword | osteogenesis | - |
dc.subject.keyword | periodontitis | - |
dc.subject.keyword | sclerostin protein, rat | - |
dc.subject.keyword | tumor necrosis factor-α | - |
dc.contributor.alternativeName | Bak, Eun-Jung | - |
dc.contributor.alternativeName | Yoo, Yun Jung | - |
dc.contributor.alternativeName | Lee, Dong Eun | - |
dc.contributor.alternativeName | Cha, Jung Heon | - |
dc.contributor.affiliatedAuthor | Bak, Eun-Jung | - |
dc.contributor.affiliatedAuthor | Yoo, Yun Jung | - |
dc.contributor.affiliatedAuthor | Lee, Dong Eun | - |
dc.contributor.affiliatedAuthor | Cha, Jung Heon | - |
dc.rights.accessRights | not free | - |
dc.citation.volume | 86 | - |
dc.citation.number | 8 | - |
dc.citation.startPage | 1005 | - |
dc.citation.endPage | 1011 | - |
dc.identifier.bibliographicCitation | JOURNAL OF PERIODONTOLOGY, Vol.86(8) : 1005-1011, 2015 | - |
dc.identifier.rimsid | 30416 | - |
dc.type.rims | ART | - |
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