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Immediate and delayed treatment with gabapentin, carbamazepine and CNQX have almost similar impact on cognitive functions and behavior in the lithium-pilocarpine model in rats

dc.contributor.authorSüyen, Güldal Güleç
dc.contributor.authorŞengün, Ece
dc.contributor.buuauthorİşbil, Naciye Büyükcoşkun
dc.contributor.buuauthorKahveci, Nevzat
dc.contributor.buuauthorÖzlük, Kasım
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentFizyoloji Ana Bilim Dalı
dc.contributor.orcid0000-0003-0841-8201
dc.contributor.researcheridAAG-7070-2021
dc.contributor.researcheridAAH-1692-2021
dc.contributor.scopusid55665951400
dc.contributor.scopusid6602597846
dc.contributor.scopusid6602676331
dc.date.accessioned2023-04-05T11:24:54Z
dc.date.available2023-04-05T11:24:54Z
dc.date.issued2016-07-13
dc.description.abstractIn the present study, we aimed to investigate the effects of immediate and delayed treatment with intracerebroventricular (i.c.v.) gabapentin (GBP), carbamazepine (CBZ) and 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) on learning and memory, anxiety, and locomotor activity in rats with lithium-pilocarpine-induced status epilepticus (SE). SE was induced by intraperitoneal injections of 3 mEq/kg LiCl followed by 45 mg/kg pilocarpine 24 h later. In the first series of experiments, rats were divided into four groups three hours after the onset of SE and received GBP (100 mu g/10 mu l, two times a day; i.c.v.), CBZ (200 mu g/10 mu l; i.c.v.), CNQX (25 nmol/10 mu l; i.c.v.) or saline (10 mu l; i.c.v.) for 7 days. Six weeks after SE, cognitive and behavioral performances were evaluated by Morris water maze, elevated plus maze, and open field tests. In the second series, rats received no treatment for six weeks following SE. On the seventh week the same treatment with the previous rats was given and six weeks later the cognitive and behavioral tests were applied. SE significantly impaired spatial learning and memory in the Morris water maze. GBP treatment improved the acqusition and memory performance. CNQX worsened the acqusition but improved the memory performance, while CBZ worsened both parameters. In the elevated plus maze, epileptic rats which received saline showed significantly lower anxiety levels with respect to the naive rats. Only CBZ led to further anxiolysis, while the other drugs had no effect Locomotor activity significantly increased due to SE, which was augmented by GBP and CNQX. The impact of immediate and delayed treatment with these drugs on cognition and behavior seems to be quite similar.
dc.identifier.citationSüyen, G. G. vd. (2016). "Immediate and delayed treatment with gabapentin, carbamazepine and CNQX have almost similar impact on cognitive functions and behavior in the lithium-pilocarpine model in rats". Pharmacology Biochemistry and Behavior, 148, 128-135.
dc.identifier.doi10.1016/j.pbb.2016.07.003
dc.identifier.endpage135
dc.identifier.issn0091-3057
dc.identifier.pubmed27426469
dc.identifier.scopus2-s2.0-84978422663
dc.identifier.startpage128
dc.identifier.urihttps://doi.org/10.1016/j.pbb.2016.07.003
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0091305716301228
dc.identifier.urihttp://hdl.handle.net/11452/32198
dc.identifier.volume148
dc.identifier.wos000382347800018
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherElsevier
dc.relation.bapT-2004/64
dc.relation.collaborationYurt içi
dc.relation.journalPharmacology Biochemistry and Behavior
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectBehavioral sciences
dc.subjectNeurosciences & neurology
dc.subjectPharmacology & pharmacy
dc.subjectGabapentin
dc.subjectCarbamazepine
dc.subjectCNQX
dc.subjectStatus epilepticus
dc.subjectCognitive
dc.subjectBehavior
dc.subjectRat
dc.subjectElevated plus-maze
dc.subjectSpontaneous recurrent seizures
dc.subjectInduced status epilepticus
dc.subjectNmda receptor antagonist
dc.subjectTemporal-lobe epilepsy
dc.subjectGlutamate receptors
dc.subjectObject recognition
dc.subjectMemory
dc.subjectMice
dc.subjectEpileptogenesis
dc.subject.emtree6 cyano 7 nitro 2,3 quinoxalinedione
dc.subject.emtreeCarbamazepine
dc.subject.emtreeGabapentin
dc.subject.emtreeLithium
dc.subject.emtreePilocarpine
dc.subject.emtreeSodium chloride
dc.subject.emtree4 aminobutyric acid
dc.subject.emtree6 cyano 7 nitro 2,3 quinoxalinedione
dc.subject.emtreeAmine
dc.subject.emtreeCarbamazepine
dc.subject.emtreeCyclohexanecarboxylic acid derivative
dc.subject.emtreeGabapentin
dc.subject.emtreePilocarpine
dc.subject.emtreeAdult
dc.subject.emtreeAnimal experiment
dc.subject.emtreeAnimal model
dc.subject.emtreeAnxiety
dc.subject.emtreeArticle
dc.subject.emtreeBehavior
dc.subject.emtreeCognition
dc.subject.emtreeControlled study
dc.subject.emtreeElevated plus maze test
dc.subject.emtreeEpileptic state
dc.subject.emtreeLocomotion
dc.subject.emtreeMemory
dc.subject.emtreeNonhuman
dc.subject.emtreePriority journal
dc.subject.emtreeRat
dc.subject.emtreeSpatial learning
dc.subject.emtreeTherapy delay
dc.subject.emtreeAnimal
dc.subject.emtreeAnimal behavior
dc.subject.emtreeChemically induced
dc.subject.emtreeCognition
dc.subject.emtreeDisease model
dc.subject.emtreeDrug effects
dc.subject.emtreeMale
dc.subject.emtreeMaze test
dc.subject.emtreeMotor activity
dc.subject.emtreePsychology
dc.subject.emtreeStatus epilepticus
dc.subject.emtreeWistar rat
dc.subject.mesh6-cyano-7-nitroquinoxaline-2,3-dione
dc.subject.meshAmines
dc.subject.meshAnimals
dc.subject.meshBehavior, animal
dc.subject.meshCarbamazepine
dc.subject.meshCognition
dc.subject.meshCyclohexanecarboxylic acids
dc.subject.meshDisease models, animal
dc.subject.meshGamma-aminobutyric acid
dc.subject.meshLithium
dc.subject.meshMale
dc.subject.meshMaze learning
dc.subject.meshMotor activity
dc.subject.meshPilocarpine
dc.subject.meshRats
dc.subject.meshRats, wistar
dc.subject.meshStatus epilepticus
dc.subject.scopusEpilepsy; Pilocarpine; Status Epilepticus
dc.subject.wosBehavioral sciences
dc.subject.wosNeurosciences
dc.subject.wosPharmacology & pharmacy
dc.titleImmediate and delayed treatment with gabapentin, carbamazepine and CNQX have almost similar impact on cognitive functions and behavior in the lithium-pilocarpine model in rats
dc.typeArticle
dc.wos.quartileQ2
dc.wos.quartileQ3 (Neurosciences)
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Fizyoloji Ana Bilim Dalı
local.indexed.atScopus
local.indexed.atWOS

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