The effects of oxytocin on penile tissues in experimental priapism model in rats

dc.contributor.author Kolukçu, Engin
dc.contributor.author Kılıç, Şahin
dc.contributor.author Parlaktaş, Bekir Süha
dc.contributor.author Erdemir, Fikret
dc.contributor.author Ünsal, Velid
dc.contributor.author Atılgan, Doğan
dc.contributor.author Uluocak, Nihat
dc.contributor.other 09.03. Department of Nutrition and Dietetics/ Beslenme ve Diyetetik Bölümü
dc.contributor.other 9. Faculty of Health Sciences / Sağlık Bilimleri Fakültesi
dc.contributor.other 01. Mardin Artuklu University / Mardin Artuklu Üniversitesi
dc.date.accessioned 14.07.201910:50:10
dc.date.accessioned 2019-07-16T20:43:49Z
dc.date.available 14.07.201910:50:10
dc.date.available 2019-07-16T20:43:49Z
dc.date.issued 2019
dc.description.abstract PurposeThis study aimed to demonstrate the effects of oxytocin on penile tissues in ischemia-reperfusion injury developed after priapism.MethodsForty Wistar Albino strain male rats were divided into four groups. The control group (n=10) was not intervened. In Group 2, a rat model of priapism was constructed and maintained for 1 h. In Group 3, reperfusion was ensured for 30min following priapism. Rats in Group 4 rats were given oxytocin 30min before the induction of reperfusion following priapism. All rats were penectomized, and adequate amounts of blood sample were drawn. Inflammation, vasocongestion, desquamation, and edema in penile tissue were scored between 0 and 3 points (0: normal, 1: mild, 2: moderate, 3: severe) to evaluate the severity of tissue damage. The activities of superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px), and the levels of malondialdehyde (MDA), and nitric oxide (NO) in blood samples were determined spectrophotometrically.ResultsIn histopathological examination, statistically significant positive changes were detected in vasocongestion, inflammation, desquamation, and edema scores in Group 4 than in Group 2 and Group 3 (p<0.001). Biochemical test results revealed that NO levels were significantly lower in Group 4 than in Group 3 (p<0.001). Serum GSH-Px activities in Group 4 significantly increased when compared with the other groups 2 and 3 (p=0.002, p=0.001, respectively). There was no statistical difference among the groups regarding SOD activities and MDA levels (p>0.05).ConclusionsOxytocin protected against priapism-induced ischemia-reperfusion injury developed in cavernosal tissue as observed based on histopathological and biochemical evidence. Although this is an experimental study, oxytocin can be thought as an alternative drug in the treatment of priapism. en_US
dc.identifier.doi 10.1007/s11255-018-2046-z
dc.identifier.issn 0301-1623
dc.identifier.issn 1573-2584
dc.identifier.scopus 2-s2.0-85057719793
dc.identifier.uri https://doi.org/10.1007/s11255-018-2046-z
dc.identifier.uri https://hdl.handle.net/20.500.12514/1224
dc.indekslendigikaynak Web of Science en_US
dc.indekslendigikaynak Scopus en_US
dc.indekslendigikaynak PubMed en_US
dc.language.iso en en_US
dc.publisher SPRINGER en_US
dc.relation.ispartof INTERNATIONAL UROLOGY AND NEPHROLOGY en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Ischemia-reperfusion injury en_US
dc.subject Oxytocin en_US
dc.subject Penile tissue en_US
dc.subject Priapism en_US
dc.subject Rat model en_US
dc.title The effects of oxytocin on penile tissues in experimental priapism model in rats en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.institutional Ünsal, Velid
gdc.author.institutional Unsal, Velid
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department MAÜ, Fakülteler, Sağlık Bilimleri Fakültesi, Beslenme ve Diyetetik Bölümü en_US
gdc.description.endpage 238 en_US
gdc.description.issue 2 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q2
gdc.description.startpage 231 en_US
gdc.description.volume 51 en_US
gdc.description.wosquality Q3
gdc.identifier.pmid 30515737
gdc.identifier.wos WOS:000459537700007
gdc.openalex.fwci 0.0
gdc.scopus.citedcount 2
gdc.wos.citedcount 3
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