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dc.contributor.authorÜnal, Orçun
dc.contributor.authorUlukan, Mustafa Özer
dc.contributor.authorBakuy, Vedat
dc.contributor.authorKaytaz, Behiye
dc.contributor.authorArtan, Sevilhan
dc.contributor.authorAral, Erinç
dc.contributor.authorÖztaş, Didem Melis
dc.contributor.authorBeyaz, Metin Onur
dc.contributor.authorUğurlucan, Murat
dc.contributor.authorSevin, Behçet
dc.date.accessioned2020-11-13T07:01:30Z
dc.date.available2020-11-13T07:01:30Z
dc.date.issued2020en_US
dc.identifier.citationÜnal, O., Ulukan, M. Ö., Bakuy, V., Kaytaz, B., Artan, S., Aral, E. ... Sevin, B. (2020). Comparison of the apoptotic effects of topically applied papaverine, diltiazem, and nitroprusside to internal thoracic artery. Brazilian Journal of Cardiovascular Surgery, 35(5), 626-633. https://dx.doi.org/10.21470/1678-9741-2019-0251en_US
dc.identifier.issn0102-7638
dc.identifier.issn1678-9741
dc.identifier.urihttps://dx.doi.org/10.21470/1678-9741-2019-0251
dc.identifier.urihttps://hdl.handle.net/20.500.12511/6026
dc.description.abstractObjective: To detect and to compare the apoptotic effects of intraoperatively topically applied diltiazem, papaverine, and nitroprusside.Methods: Internal thoracic artery segments of ten patients were obtained during coronary bypass grafting surgery. Each internal thoracic artery segment was divided into four pieces and immersed into four different solutions containing separately saline (Group S), diltiazem (Group D), papaverine (Group P), and nitroprusside (Group N). Each segment was examined with both hematoxylin-eosin and the terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling (TUNEL) method in order to determine and quantify apoptosis.Results: Apoptotic cells were counted in 50 microscopic areas of each segment. No significant difference was observed among the four groups according to hematoxylin-eosin staining. However, the TUNEL method revealed a significant increase in mean apoptotic cells in the diltiazem group when compared with the other three groups (Group S=4.25 +/- 1.4; Group D=13.31 +/- 2.8; Group N=9.48 +/- 2.09; Group P=10.75 +/- 2.37). The differences between groups were significant (P=0.0001). No difference was observed between the samples of the diabetic and non-diabetic patients in any of the study groups.Conclusion: The benefit of topically applied vasodilator drugs must outweigh the potential adverse effects. In terms of apoptosis, diltiazem was found to have the most deleterious effects on internal thoracic artery graft segments. Of the analyzed medical agents, nitroprusside was found to have the least apoptotic activity, followed by papaverine. Diabetes did not have significant effect on the occurrence of apoptosis in left internal thoracic artery grafts.en_US
dc.description.sponsorshipEskisehir Osmangazi University Medical Faculty, Eskisehir, Turkeyen_US
dc.language.isoengen_US
dc.publisherSociedade Brasileira de Cirurgia Cardiovascularen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAttribution 4.0 International*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subjectMammary Arteriesen_US
dc.subjectVasodilatador Agentsen_US
dc.subjectCoronary Artery Bypassen_US
dc.subjectApoptosisen_US
dc.subjectDiabetes Mellitusen_US
dc.subjectDiltiazemen_US
dc.subjectBiotinen_US
dc.subjectHematoxylinen_US
dc.titleComparison of the apoptotic effects of topically applied papaverine, diltiazem, and nitroprusside to internal thoracic arteryen_US
dc.typearticleen_US
dc.relation.ispartofBrazilian Journal of Cardiovascular Surgeryen_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Kalp ve Damar Cerrahisi Ana Bilim Dalıen_US
dc.authorid0000-0001-9919-8392en_US
dc.authorid0000-0001-9338-8152en_US
dc.authorid0000-0001-6643-9364en_US
dc.identifier.volume35en_US
dc.identifier.issue5en_US
dc.identifier.startpage626en_US
dc.identifier.endpage633en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.21470/1678-9741-2019-0251en_US
dc.identifier.wosqualityQ4en_US
dc.identifier.scopusqualityQ3en_US


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