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dc.contributor.authorTekin, Gozde
dc.contributor.authorIsbir, Selim
dc.contributor.authorSener, Goksel
dc.contributor.authorCevik, Ozge
dc.contributor.authorCetinel, Sule
dc.contributor.authorDericioglu, Okan
dc.contributor.authorArsan, Sinan
dc.contributor.authorCobanoglu, Adnan
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T09:38:11Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T09:38:11Z
dc.date.issued2018
dc.identifier.issn0741-5214
dc.identifier.urihttps://dx.doi.org/10.1016/j.jvs.2017.04.028
dc.identifier.urihttps://hdl.handle.net/20.500.12418/6284
dc.descriptionWOS: 000430919000030en_US
dc.descriptionPubMed ID: 28478022en_US
dc.description.abstractObjective: Oxygen free radicals are important components involved in the histopathologic tissue alterations observed during abdominal aortic aneurysms (AAAs). This study examined whether melatonin has protective or therapeutic effects against AAAs. Methods: Sprague-Dawley rats were divided into four groups. A CaCl2 model was used to induce AAA. Starting on the operation day (Mel+AAA+Mel group) or 4 weeks after the operation (AAA+Mel group), the rats received intraperitoneal melatonin (10 mg/kg/day) for 6 and 2 weeks, respectively. The control and AAA groups received vehicle for 2 weeks after the sham operation and AAA induction, respectively. Angiographic measurements were recorded at the beginning, week 4, and week 6 of the study. After decapitation, aorta tissues were taken for the measurement of malondialdehyde, 8-hydroxy-2'-deoxyguanosine, glutathione levels, and myeloperoxidase and caspase-3 activity. Matrix metalloproteinase (MMP)-2, MMP-9, tumor necrosis factor-a, and inducible nitric oxide synthase protein expressions were analyzed by Western blot technique. Aortic tissues were also examined by light microscopy. Results: CaCl2 caused an inflammatory response and oxidative damage indicated by rises in malondialdehyde and 8-hydroxy-2'-deoxyguanosine levels. Myeloperoxidase and caspase-3 activities were increased, but glutathione levels were reduced. On the one hand, MMP-2, MMP-9, tumor necrosis factor-a, and inducible nitric oxide synthase protein expressions were increased in the vehicle-treated AAA group. On the other hand, melatonin treatment reversed all of these biochemical indices and histopathologic alterations. Conclusions: According to the data, although melatonin tended to reverse the biochemical parameters given on week 4, the preventive effect is more pronounced when given concomitantly with AAA induction because values were closer to the control levels.en_US
dc.description.sponsorshipMarmara University Scientific Research Projects Commission [SAG-C-TUP-12114-0355]en_US
dc.description.sponsorshipThis project was supported by Marmara University Scientific Research Projects Commission (project no: SAG-C-TUP-12114-0355).en_US
dc.language.isoengen_US
dc.publisherMOSBY-ELSEVIERen_US
dc.relation.isversionof10.1016/j.jvs.2017.04.028en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleThe preventive and curative effects of melatonin against abdominal aortic aneurysm in ratsen_US
dc.typearticleen_US
dc.relation.journalJOURNAL OF VASCULAR SURGERYen_US
dc.contributor.department[Tekin, Gozde -- Isbir, Selim -- Dericioglu, Okan -- Arsan, Sinan -- Cobanoglu, Adnan] Marmara Univ, Sch Med, Dept Cardiovasc Surg, Istanbul, Turkey -- [Sener, Goksel] Marmara Univ, Dept Pharmacol, Sch Pharm, Istanbul, Turkey -- [Cevik, Ozge] Cumhuriyet Univ, Sch Pharm, Dept Biochem, Sivas, Turkey -- [Cetinel, Sule] Marmara Univ, Sch Med, Dept Histol & Embryol, Istanbul, Turkeyen_US
dc.contributor.authorIDArsan, Sinan -- 0000-0002-0890-2506; Cevik, Ozge -- 0000-0002-9325-3757en_US
dc.identifier.volume67en_US
dc.identifier.issue5en_US
dc.identifier.endpage1555en_US
dc.identifier.startpage1546en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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