The antimanic-like effect of phenytoin and carbamazepine on methylphenidate-induced hyperlocomotion: role of voltage-gated sodium channels

The objective of this study was to verify whether phenytoin modifies methylphenidate‐induced hyperlocomotion, an animal model for screening antimanic‐like drugs, and also evaluate the effect of veratrine, a voltage‐gated sodium channel opener, pretreatment on the effect of phenytoin in this model. C...

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Published in:Fundamental & clinical pharmacology Vol. 27; no. 6; pp. 650 - 655
Main Authors: Tonelli, Denise A.G., Pereira, Marcela, Siba, Isadora P., Martynhak, Bruno J., Correia, Diego, Casarotto, Plínio C., Biojone, Caroline, Guimarães, Francisco S., Joca, Samia L.R., Andreatini, Roberto
Format: Journal Article
Language:English
Published: Oxford Blackwell Publishing Ltd 01-12-2013
Blackwell
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Summary:The objective of this study was to verify whether phenytoin modifies methylphenidate‐induced hyperlocomotion, an animal model for screening antimanic‐like drugs, and also evaluate the effect of veratrine, a voltage‐gated sodium channel opener, pretreatment on the effect of phenytoin in this model. Carbamazepine was used as a positive control. Methylphenidate (5 mg/kg, s.c.) increased open‐field locomotion, and phenytoin (5–10 mg/kg, i.p.) and carbamazepine (20 mg/kg, i.p.) blocked this effect. Veratrine (0.4 mg/kg, s.c.) pretreatment reversed the effects of phenytoin (10 mg/kg, i.p.) and carbamazepine (20 mg/kg, i.p.). Phenytoin (1–50 mg/kg, i.p.) and carbamazepine (10–20 mg/kg i.p.) alone did not change spontaneous locomotor activity. These results indicate that voltage‐gated sodium channels play an important role in antimanic‐like effects of phenytoin and carbamazepine on psychostimulant‐induced hyperlocomotion model.
Bibliography:ark:/67375/WNG-SPJBJJF5-5
istex:722A5A2E133F373C43DA12AED466F86A5F663BA8
ArticleID:FCP12022
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0767-3981
1472-8206
DOI:10.1111/fcp.12022