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dc.contributor.authorAricioglu, F
dc.contributor.authorYillar, O
dc.contributor.authorKorcegez, E
dc.contributor.authorBerkman, K
dc.date.accessioned2021-03-03T15:58:19Z
dc.date.available2021-03-03T15:58:19Z
dc.identifier.citationAricioglu F., Yillar O., Korcegez E., Berkman K., "Effect of harmane on the convulsive threshold in epilepsy models in mice", AGMATINE AND IMIDAZOLINES: THEIR NOVEL RECEPTORS AND ENZYMES, cilt.1009, ss.190-195, 2003
dc.identifier.issn0077-8923
dc.identifier.othervv_1032021
dc.identifier.otherav_41be1856-482b-4b04-9a35-f77b50fa8e0a
dc.identifier.urihttp://hdl.handle.net/20.500.12627/47926
dc.identifier.urihttps://doi.org/10.1196/annals.1304.023
dc.description.abstractThe study investigated the activity of harmane on maximal electroshock seizures (MES) and seizures induced by pentilentetrazole (PTZ) in mice. Initial studies established convulsive current 50 (CC50) values or MES and effective dose 50 (ED50) for PTZ to produce seizures. Harmane (2.5, 5.0, or 10 mg/kg intraperitoneally) increased the threshold of seizures in MES dose-dependently. The convulsions produced by PTZ were decreased by the low dose of harmane (2.5 mg/kg), but the high dose of harmane (10 mg/kg) resulted in worse grade V convulsions followed by more lethality compared with PTZ alone. Therefore, harmane seems to be protective against grand mal seizures in the MES model but not against a petit mal seizure model (PTZ) in mice.
dc.language.isoeng
dc.subjectSinirbilim ve Davranış
dc.subjectFARMAKOLOJİ VE ECZACILIK
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectSağlık Bilimleri
dc.subjectEczacılık
dc.subjectTemel Eczacılık Bilimleri
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectSitogenetik
dc.subjectTemel Bilimler
dc.subjectTemel Bilimler (SCI)
dc.subjectNEUROSCIENCES
dc.subjectDoğa Bilimleri Genel
dc.subjectÇOK DİSİPLİNLİ BİLİMLER
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectBİYOKİMYA VE MOLEKÜLER BİYOLOJİ
dc.titleEffect of harmane on the convulsive threshold in epilepsy models in mice
dc.typeMakale
dc.relation.journalAGMATINE AND IMIDAZOLINES: THEIR NOVEL RECEPTORS AND ENZYMES
dc.contributor.department, ,
dc.identifier.volume1009
dc.identifier.startpage190
dc.identifier.endpage195
dc.contributor.firstauthorID167231


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