Publication:
Interaction of Leptin and Nitric Oxide Pathway on Penicillin-Induced Epileptiform Activity in Rats

dc.authorscopusid7102214656
dc.authorscopusid57207157391
dc.authorscopusid6602693377
dc.authorscopusid8709976000
dc.authorscopusid7003281190
dc.contributor.authorAslan, A.
dc.contributor.authorYildirim, M.
dc.contributor.authorAyyildiz, M.
dc.contributor.authorGüven, A.
dc.contributor.authorAǧar, E.
dc.date.accessioned2020-06-21T14:52:32Z
dc.date.available2020-06-21T14:52:32Z
dc.date.issued2010
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Aslan] Ali, Department of Physiology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Yildirim] Mehmet Iskender, Department of Physiology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Ayyildiz] Mustafa, Department of Physiology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Güven] Ayla, Department of Pediatric Endocrinology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Aǧar] Erdal, Department of Physiology, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractThe aim of the present study was to investigate the role of NO as a mediator of leptin action at the penicillin-induced epileptiform activity in rat. Thirty minutes after penicillin injection, leptin, at a dose of 1 μg, significantly increased the mean frequency of epileptiform activity without changing the amplitude. The effects of systemic administration of nitric oxide synthase (NOS) inhibitors, non-selective NG-nitro-l-arginine methyl ester (L-NAME), selective neuronal NOS inhibitor, 7-nitroindazole (7-NI) and NO precursor, l-arginine on the effects of leptin were investigated. The occurrence of anticonvulsant activity of 7-NI (40 mg/kg, i.p.) was significantly delayed in the presence of leptin (1 μg). The administration of L-NAME (60 mg/kg, i.p.), 30 min before leptin (1 μg) application, did not influence proconvulsant activity of leptin. The administration of l-arginine (1000 mg/kg, i.p.) 30 min before the effective dose of leptin (1 μg, i.c.v.) reversed the proconvulsant effects of leptin whereas the same dose of its inactive enantiomer, d-arginine (1000 mg/kg, i.p.) failed to influence the proconvulsant effect of leptin. The electrophysiological evidence of the present study suggests that neuronal NOS/NO pathway is involved in mediating leptin effects on penicillin-induced epileptiform activity. © 2010 Elsevier B.V. All rights reserved.en_US
dc.identifier.doi10.1016/j.brainres.2010.01.054
dc.identifier.endpage124en_US
dc.identifier.issn0006-8993
dc.identifier.issn1872-6240
dc.identifier.pmid20116371
dc.identifier.scopus2-s2.0-77549086359
dc.identifier.scopusqualityQ3
dc.identifier.startpage117en_US
dc.identifier.urihttps://doi.org/10.1016/j.brainres.2010.01.054
dc.identifier.volume1321en_US
dc.identifier.wosWOS:000276120800013
dc.identifier.wosqualityQ3
dc.language.isoenen_US
dc.publisherElsevier Science BVen_US
dc.relation.ispartofBrain Researchen_US
dc.relation.journalBrain Researchen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject7-Nien_US
dc.subjectEpileptiform Activityen_US
dc.subjectL-NAMEen_US
dc.subjectLeptinen_US
dc.subjectNOSen_US
dc.titleInteraction of Leptin and Nitric Oxide Pathway on Penicillin-Induced Epileptiform Activity in Ratsen_US
dc.typeArticleen_US
dspace.entity.typePublication

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