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dc.contributor.authorYuce, H. Balci
dc.contributor.authorAlpan, A. Lektemur
dc.contributor.authorGevrek, F.
dc.contributor.authorToker, H.
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T09:38:40Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T09:38:40Z
dc.date.issued2018
dc.identifier.issn0022-3484
dc.identifier.issn1600-0765
dc.identifier.urihttps://dx.doi.org/10.1111/jre.12497
dc.identifier.urihttps://hdl.handle.net/20.500.12418/6388
dc.descriptionWOS: 000419401200016en_US
dc.descriptionPubMed ID: 29044575en_US
dc.description.abstractBackground and ObjectiveAstaxanthin is a keto-carotenoid that has a strong antioxidant effect. The purpose of this study was to evaluate the effects of astaxanthin on alveolar bone loss and histopathological changes in ligature-induced periodontitis in rats. Material and methodsWistar rats were divided into four experimental groups: non-ligated (C, n=6); ligature only (L, n=6); ligature and astaxanthin (1mg/kg/day astaxanthin, AS1 group, n=8); ligature and astaxanthin (5mg/kg/day astaxanthin, AS5 group, n=8). Silk ligatures were placed at the gingival margin of lower first molars of the mandibular quadrant. The study duration was 11days and the animals were killed at the end of this period. Changes in alveolar bone levels were clinically measured and tissues were immunohistochemically examined, osteocalcin, bone morphogenic protein-2, inducible nitric oxide synthase, Bax and bcl-2 levels in alveolar bone and tartrate-resistant acid phosphatase-positive osteoclast cells, osteoblast and inflammatory cell counts were determined. ResultsAlveolar bone loss was highest in the L group and the differences among the L, AS1 and AS5 groups were also significant (P<.05). Both doses of astaxanthin decreased tartrate-resistant acid phosphatase-positive+ osteoclast cell and increased osteoblast cell counts (P<.05). The inflammation in the L group was also higher than those of the C and AS1 groups were (P<.05) indicating the anti-inflammatory effect of astaxanthin. Although inducible nitric oxide synthase, osteocalcin, bone morphogenic protein-2 and bax staining percentages were all highest in the AS5 group and bcl-2 staining percentage was highest in the AS1 group, values were close to each other (P>.05). ConclusionWithin the limits of this study, it can be suggested that astaxanthin administration may reduce alveolar bone loss by increasing osteoblastic activity and decrease osteoclastic activity in experimental periodontitis model.en_US
dc.language.isoengen_US
dc.publisherWILEYen_US
dc.relation.isversionof10.1111/jre.12497en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectantioxidantsen_US
dc.subjectastaxanthinen_US
dc.subjectexperimental periodontitisen_US
dc.subjectinducible nitric oxide synthaseen_US
dc.subjecttartrate-resistant acid phosphataseen_US
dc.titleInvestigation of the effect of astaxanthin on alveolar bone loss in experimental periodontitisen_US
dc.typearticleen_US
dc.relation.journalJOURNAL OF PERIODONTAL RESEARCHen_US
dc.contributor.department[Yuce, H. Balci] Gaziosmanpasa Univ, Dept Periodontol, Fac Dent, Tokat, Turkey -- [Alpan, A. Lektemur] Pamukkale Univ, Dept Periodontol, Fac Dent, Denizli, Turkey -- [Gevrek, F.] Gaziosmanpasa Univ, Fac Med, Dept Histol & Embryol, Tokat, Turkey -- [Toker, H.] Cumhuriyet Univ, Dept Periodontol, Fac Dent, Sivas, Turkeyen_US
dc.contributor.authorIDbalci yuce, hatice -- 0000-0003-3574-9751; LEKTEMUR ALPAN, AYSAN -- 0000-0002-5939-4783en_US
dc.identifier.volume53en_US
dc.identifier.issue1en_US
dc.identifier.endpage138en_US
dc.identifier.startpage131en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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