Drug Res (Stuttg) 2017; 67(03): 179-182
DOI: 10.1055/s-0042-121419
Original Article
© Georg Thieme Verlag KG Stuttgart · New York

Sumatriptan, an Antimigraine Drug, Inhibits Pentylenetetrazol-induced Seizures in NMRI Mice

Abolfazl Jand
1   General Practitioner, Faculty of Medicine, Department of Physiology, Arak University of Medical Sciences, Arak, IR, Iran
,
Mohammad Reza Palizvan
2   Associate Professor, Faculty of Medicine, Department of physiology, Arak University of Medical Sciences, Arak, IR, Iran
› Author Affiliations
Further Information

Publication History

received 13 June 2016

accepted 10 November 2016

Publication Date:
11 January 2017 (online)

Abstract

Sumatriptan has been used for the acute treatment of migraine attacks. There are many similarities between migraine and epilepsy and the medications used to treat one of these disorders can effectively be used to treat the other. The purpose of this study was to evaluate and compare the anticonvulsant effects of sumatriptan with sodium valproate in NMRI mice. 62 male NMRI mice were divided into 8 groups. The groups consisted of a saline (control) group, 4 intraperitoneally (ip) administered sumatriptan groups (1, 10, 50, and 100 mg/kg, ip), and 3 sodium valproate groups (50, 150, and 300 mg/kg, ip). 20-min after the injection of either saline or one of the drug doses, pentylenetetrazol (100 mg/kg, ip) was injected and seizure parameters were evaluated. The results showed that 300 mg/kg sodium valproate markedly inhibited the seizure stage, whereas none of the sumatriptan doses had any significant effect on this parameter. The latency to stages 2 and 4 of the seizures and the interval between the pentylenetetrazol injection to death was significantly increased by both sodium valproate and sumatriptan.

Sumatriptan is commonly used for the treatment of migraine and also has a protective effect against seizures induced by pentylenetetrazol in mice.

 
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