Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/9605
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dc.contributor.authorKose, O.-
dc.contributor.authorArabaci, T.-
dc.contributor.authorKara, A.-
dc.contributor.authorYemenoglu, H.-
dc.contributor.authorKermen, E.-
dc.contributor.authorKızıldağ, Alper-
dc.contributor.authorGedikli, S.-
dc.date.accessioned2019-08-16T13:03:21Z
dc.date.available2019-08-16T13:03:21Z
dc.date.issued2016-
dc.identifier.issn0022-3492-
dc.identifier.urihttps://hdl.handle.net/11499/9605-
dc.identifier.urihttps://doi.org/10.1902/jop.2016.150541-
dc.description.abstractBackground: The aim of this study is to evaluate the effects of systemic melatonin treatment on serum oxidative stress index (OSI) and alveolar bone loss (ABL) in rats with diabetes mellitus (DM) and periodontitis. Methods: Seventy Sprague Dawley rats were divided into control, experimentally induced periodontitis (EP), DM, EPDM, EP and melatonin treatment (EP-MEL), DM and melatonin treatment (DMMEL), and EP-DM-MEL groups. DM was induced by alloxan, after which periodontitis was induced by ligature for 4 weeks. After removal of the ligature, the rats in the melatonin groups (EP-MEL, DM-MEL, and EP-DM-MEL) were treated with a single dose of melatonin (10 mg/body weight) every day for 14 consecutive days. At the end of the study, all of the rats were euthanized, and intracardiac blood samples and mandible tissues were obtained for biochemical and histologic analyses. Serum levels of total oxidant status/total antioxidant status and OSI were measured. In addition, neutrophil and osteoclast densities and myeloperoxidase activities were determined in gingival tissue homogenates, and ABL was evaluated with histometric measurements. Results: Melatonin treatment significantly reduced fasting plasma glucose levels in the rats with DM. In addition, reduced OSI and ABL levels were detected in the EP-MEL and DM-MEL groups; the reductions in the EP-DM-MEL group were found to be more prominent. Melatonin also significantly decreased the increased myeloperoxidase activities and osteoclast and neutrophil densities in the EP, DM, and EP-DM groups. Conclusion: It is revealed in this experimental study that melatonin significantly inhibited hyperglycemia-induced oxidative stress and ABL through antiDM and antioxidant effects in rats with DM and periodontitis.en_US
dc.language.isoenen_US
dc.publisherAmerican Academy of Periodontologyen_US
dc.relation.ispartofJournal of Periodontologyen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAnti-inflammatory agentsen_US
dc.subjectAntioxidantsen_US
dc.subjectDiabetes mellitusen_US
dc.subjectMelatoninen_US
dc.subjectOxidative stressen_US
dc.subjectPeriodontitisen_US
dc.subjectantioxidanten_US
dc.subjectmelatoninen_US
dc.subjectalveolar bone lossen_US
dc.subjectanimalen_US
dc.subjectexperimental diabetes mellitusen_US
dc.subjectmetabolismen_US
dc.subjectoxidative stressen_US
dc.subjectpathophysiologyen_US
dc.subjectperiodontitisen_US
dc.subjectphysiologyen_US
dc.subjectraten_US
dc.subjectSprague Dawley raten_US
dc.subjectWistar raten_US
dc.subjectAlveolar Bone Lossen_US
dc.subjectAnimalsen_US
dc.subjectDiabetes Mellitus, Experimentalen_US
dc.subjectOxidative Stressen_US
dc.subjectRatsen_US
dc.subjectRats, Sprague-Dawleyen_US
dc.subjectRats, Wistaren_US
dc.titleEffects of melatonin on oxidative stress index and alveolar bone loss in diabetic rats with periodontitisen_US
dc.typeArticleen_US
dc.identifier.volume87en_US
dc.identifier.issue5en_US
dc.identifier.startpagee82
dc.identifier.startpagee82en_US
dc.identifier.endpagee90en_US
dc.identifier.doi10.1902/jop.2016.150541-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid26832833en_US
dc.identifier.scopus2-s2.0-84962704111en_US
dc.identifier.wosWOS:000375843400004en_US
dc.identifier.scopusqualityQ1-
dc.ownerPamukkale University-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairetypeArticle-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
crisitem.author.dept06.01. Clinical Sciences-
Appears in Collections:Diş Hekimliği Fakültesi Koleksiyonu
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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