Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/31669
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dc.contributor.authorJensen, Morten Skovgaard-
dc.contributor.authorDansher, Gorm-
dc.date.accessioned2023-03-21T10:54:20Z-
dc.date.available2023-03-21T10:54:20Z-
dc.date.issued2007-07-
dc.identifier.citationNoyan, B. vd. (2007). "The lack of effects of zinc and nitric oxide in initial state of pilocarpine-induced seizures". Renewable Energy, 16(5), 410-416.en_US
dc.identifier.issn1059-1311-
dc.identifier.issn1532-2688-
dc.identifier.urihttps://doi.org/10.1016/j.seizure.2007.02.012-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S1059131107000532-
dc.identifier.urihttp://hdl.handle.net/11452/31669-
dc.description.abstractIn this study we investigated whether intracerebroventricular (i.c.v.) injection Of L-NAME (a nitric oxide synthase inhibitor) or CaEDTA (an extracellular zinc chetator) or the combination of the two could affect the initial phase of pitocarpine induced (2 h) seizures. Two groups of rats were used. Animals from both groups were given with i.c.v. injections of either saline (10 mu), L-NAME (150 mu g/10l), CaEDTA (100 mM/10 mu l) or L-NAME and CaEDTA. One group received pilocarpine HCl (380 mg/ kg i.p.) the other served as control. Pilocarpine HCI. was injected intraperitoneally 10 min later. The behavior of the animals was observed for 2 h and the intensity of their seizures was scored. The rats were then sacrificed and their brains were removed and analyzed for zinc ions by using the immersion autometatlography and the TSQ fluorescence staining. All the animals which received pilocarpine HCl developed seizures. Despite treatment with L-NAME and/or CaEDTA we found that the Latency and the intensity of seizures were similar in both groups investigated. The distribution of stainable zinc ions and the intensity of staining in hippocampus were not affected by pilocarpine and found unchanged after L-NAME and/or CaEDTA injections in both the control animals and the pilocarpine treated animals. The data suggest that the nitric oxide system and zinc ions do not affect pilocarpine-induced seizures in their initial state.en_US
dc.language.isoenen_US
dc.publisherWB Saundersen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAtıf Gayri Ticari Türetilemez 4.0 Uluslararasıtr_TR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectImmersion AMGen_US
dc.subjectNeurosciences & neurologyen_US
dc.subjectSynaptically-released zincen_US
dc.subjectNitric oxideen_US
dc.subjectSeizureen_US
dc.subjectTSQ fluorescenceen_US
dc.subjectZincen_US
dc.subjectMuscarinic receptor subtypesen_US
dc.subjectAcid-induced seizuresen_US
dc.subjectChelatable zincen_US
dc.subjectIn-vivoen_US
dc.subjectAnticonvulsanten_US
dc.subjectActivationen_US
dc.subjectMk-801en_US
dc.subjectInjuryen_US
dc.subjectZn2+en_US
dc.subject.meshAnimalsen_US
dc.subject.meshDisease models, animalen_US
dc.subject.meshEdetic aciden_US
dc.subject.meshBehavior, animalen_US
dc.subject.meshChelating agentsen_US
dc.subject.meshDrug interactionsen_US
dc.subject.meshNitric oxideen_US
dc.subject.meshEnzyme inhibitorsen_US
dc.subject.meshNG-nitroarginine methyl esteren_US
dc.subject.meshFunctional lateralityen_US
dc.subject.meshInjections, intraventricularen_US
dc.subject.meshHippocampusen_US
dc.subject.meshMaleen_US
dc.subject.meshPilocarpineen_US
dc.subject.meshRatsen_US
dc.subject.meshRats, sprague-dawleyen_US
dc.subject.meshSeizuresen_US
dc.subject.meshZincen_US
dc.titleThe lack of effects of zinc and nitric oxide in initial state of pilocarpine-induced seizuresen_US
dc.typeArticleen_US
dc.identifier.wos000247726900005tr_TR
dc.identifier.scopus2-s2.0-34249703370tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Fizyoloji Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0002-3984-496Xtr_TR
dc.identifier.startpage410tr_TR
dc.identifier.endpage416tr_TR
dc.identifier.volume16tr_TR
dc.identifier.issue5tr_TR
dc.relation.journalSeizure European Journal of Epilepsyen_US
dc.contributor.buuauthorNoyan, Behzat-
dc.relation.collaborationYurt dışıtr_TR
dc.identifier.pubmed17376708tr_TR
dc.subject.wosClinical neurologyen_US
dc.subject.wosNeurosciencesen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubmeden_US
dc.wos.quartileQ3en_US
dc.contributor.scopusid6506333172tr_TR
dc.subject.scopusHomocysteine Thiolactone; Thioesters; Cystathionineen_US
dc.subject.emtreeAnimal tissueen_US
dc.subject.emtreeAnimal behavioren_US
dc.subject.emtreeAnimal experimenten_US
dc.subject.emtreeAnimal modelen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreePilocarpineen_US
dc.subject.emtreeCombination chemotherapyen_US
dc.subject.emtreeN(g) nitroarginine methyl esteren_US
dc.subject.emtreeAutometallographyen_US
dc.subject.emtreeBrain surgeryen_US
dc.subject.emtreeClinical observationen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeEdetate calciumen_US
dc.subject.emtreeFluorescence analysisen_US
dc.subject.emtreeScoring systemen_US
dc.subject.emtreeDisease severityen_US
dc.subject.emtreeHippocampusen_US
dc.subject.emtreeNitric oxideen_US
dc.subject.emtreeHistochemistryen_US
dc.subject.emtreeLatent perioden_US
dc.subject.emtreeSeizureen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeMonotherapyen_US
dc.subject.emtreeNonhumanen_US
dc.subject.emtreePriority journalen_US
dc.subject.emtreeRaten_US
dc.subject.emtreeSodium chlorideen_US
dc.subject.emtreeToluenesulfonamide derivativeen_US
dc.subject.emtreeZincen_US
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