Please use this identifier to cite or link to this item: http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/4765
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dc.contributor.authorTatar, Arzu-
dc.contributor.authorKorkmaz, Mukadder-
dc.contributor.authorYayla, Muhammed-
dc.contributor.authorPolat, Elif-
dc.contributor.authorUslu, Hakan-
dc.contributor.authorHalici, Zekai-
dc.contributor.authorParlak, Secil N.-
dc.date.accessioned2024-03-19T06:57:28Z-
dc.date.available2024-03-19T06:57:28Z-
dc.date.issued2017-
dc.identifier.citationTatar, A., Korkmaz, M., Yayla, M., Polat, E., Uslu, H., Halici, Z., Parlak, SN. (2017). The potential role of amlodipine on experimentally induced bacterial rhinosinusitis. Braz. J. Otorhinolaryngol., 83(6), 619-626. https://doi.org/10.1016/j.bjorl.2016.08.006en_US
dc.identifier.issn1808-8694-
dc.identifier.issn1808-8686-
dc.identifier.urihttp://dx.doi.org/10.1016/j.bjorl.2016.08.006-
dc.identifier.urihttps://www.webofscience.com/wos/woscc/full-record/WOS:000417392200003-
dc.identifier.urihttp://earsiv.odu.edu.tr:8080/xmlui/handle/11489/4765-
dc.descriptionWoS Categories: Otorhinolaryngologyen_US
dc.descriptionWeb of Science Index: Science Citation Index Expanded (SCI-EXPANDED)en_US
dc.descriptionResearch Areas: Otorhinolaryngologyen_US
dc.description.abstractIntroduction: Antibiotics are frequently used for the treatment of rhinosinusitis. Concerns have been raised regarding the adverse effects of antibiotics and growing resistance. The lack of development of new antibiotic compounds has increased the necessity for exploration of non-antibiotic compounds that have antibacterial activity. Amlodipine is a non-antibiotic compound with anti-inflammatory activity. Objective: In this study we aimed to investigate the potential role of amlodipine in the treatment of rhinosinusitis by evaluating its effects on tissue oxidative status, mucosal histology and inflammation. Methods: Fifteen adult albino guinea pigs were inoculated with Staphylococcus aureus and treated with saline, cefazolin sodium, or amlodipine for 7 days. The control group was composed by five healthy guinea pigs. Animals were sacrificed after the treatment. Histopathological changes were identified using Hematoxylin-Eosin staining. Inflammation was assessed by Polymorphonuclear Leukocyte infiltration density. Tissue levels of antioxidants (superoxide dismutase, glutathione) and an oxidative product (malondialdehyde) were determined. Results: In rhinosinusitis induced animals, amlodipine reduced loss of cilia, lamina propria edema and collagen deposition compared to placebo (saline) and although not superior to cefazolin, amlodipine decreased polymorphonuclear leukocyte infiltration. The superoxide dismutase activity and glutathione levels were reduced, whereas the malondialdehyde levels were increased significantly in all three-treatment groups compared to the control group. Amlodipine treated group showed significantly increased superoxide dismutase and glutathione levels and decreased malondialdehyde levels compared to all treatment groups. Conclusion: The non-antibiotic compound amlodipine may have a role in acute rhinosinusitis treatment through tissue protective, antioxidant and anti-inflammatory mechanisms. (C) 2016 Associacao Brasileira de Otorrinolaringologia e Cirurgia Cervico-Facial. Published by Elsevier Editora Ltda.en_US
dc.language.isoengen_US
dc.publisherASSOC BRASILEIRA OTORRINOLARINGOLOGIA & CIRURGIA CERVICOFACIAL-SAO PAULOen_US
dc.relation.isversionof10.1016/j.bjorl.2016.08.006en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectRhinosinusitis, Non-antibiotic, Amlodipine, Antioxidants, Guinea pigen_US
dc.subjectIN-VITRO, ANTIBIOTICS, INFECTIONS, MANAGEMENT, TISSUE, INFLAMMASOME, ANTIOXIDANT, MECHANISMS, SINUSITIS, DAMAGEen_US
dc.titleThe potential role of amlodipine on experimentally induced bacterial rhinosinusitisen_US
dc.typearticleen_US
dc.relation.journalBRAZILIAN JOURNAL OF OTORHINOLARYNGOLOGYen_US
dc.contributor.departmentOrdu Üniversitesien_US
dc.contributor.authorID0000-0002-0659-3084en_US
dc.contributor.authorID0000-0001-6808-5467en_US
dc.identifier.volume83en_US
dc.identifier.issue6en_US
dc.identifier.startpage619en_US
dc.identifier.endpage626en_US
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