Publication:
The effect of tizanidine on maximal electroshock seizures (MES) in mice

dc.contributor.authorDENİZBAŞI ALTINOK, ARZU
dc.contributor.authorsDenizbaşi, A.; Berkman, K.; Ozyazgan, S.; Eşkazan, E.
dc.date.accessioned2022-03-15T11:11:30Z
dc.date.accessioned2026-01-11T08:25:27Z
dc.date.available2022-03-15T11:11:30Z
dc.date.issued1999
dc.description.abstractTizanidine, an alpha-2 adrenergic agonist, is a centrally active muscle relaxant and a spasmolytic drug. The aim of our study was to investigate the activity of tizanidine on maximal electroshock seizures (MES) in mice. In the first part of the study, convulsive current 50 (CC 50) value to produce seizures was found. Then, tizanidine was given intraperitoneally (IP) at the doses of 0.5, 1, and 2 mg/kg, and orally (PO) at the doses of 5, 10, 20, 40 mg/kg. We found that tizanidine at the doses of 1 and 2 mg/kg IP and 40 mg/kg PO caused a significant protection against MES. In the second part of the study, after pretreatment with yohimbine, an alpha-2 adrenergic receptor blocker, at the dose of 2 mg/kg, anticonvulsant effect of tizanidine is diminished. We concluded that the mode of action of the anticonvulsant effect of tizanidine may be mediated by the central alpha-2 adrenergic receptors.
dc.identifier.doi10.1016/s0306-3623(98)00249-3
dc.identifier.issn0306-3623
dc.identifier.pubmedPMID: 10323494
dc.identifier.urihttps://hdl.handle.net/11424/248923
dc.language.isoeng
dc.relation.ispartofGeneral Pharmacology
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectFemale
dc.subjectAnimals
dc.subjectMale
dc.subjectAdministration, Oral
dc.subjectMice
dc.subjectInjections, Intraperitoneal
dc.subjectAnticonvulsants
dc.subjectAdrenergic alpha-Antagonists
dc.subjectClonidine
dc.subjectElectroshock
dc.subjectReceptors, Adrenergic, alpha-2
dc.subjectSeizures
dc.subjectYohimbine
dc.titleThe effect of tizanidine on maximal electroshock seizures (MES) in mice
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage516
oaire.citation.startPage513
oaire.citation.titleGeneral Pharmacology
oaire.citation.volume4

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