Literature DB >> 17256170

Conventional anticonvulsant drugs in the guinea-pig kindling model of partial seizures: effects of repeated administration.

Trevor H Gilbert1, G Campbell Teskey.   

Abstract

This study addressed the anticonvulsant effects of repeated administration of phenytoin, carbamazepine, phenobarbital, valproate, and ethosuximide in kindled guinea-pigs in order to further substantiate this novel model of partial seizures for the screening of future anticonvulsant drugs. Behavioral toxic effects were assessed at 30 min following drug administration using scores on a sedation/muscle relaxation rating index. In response to suprathreshold stimulation, the anticonvulsant efficacy of the drugs were evaluated from measurements of afterdischarge duration (ADD) and behavioral seizure severity (SS) during a repeated drug treatment schedule in kindled guinea-pigs. All drugs exerted slight to moderate sedative effects in guinea-pigs on our rating index. We found that phenytoin, carbamazepine, and phenobarbital exhibited effective anticonvulsant properties in kindled guinea-pigs by reducing both ADD and SS. We found that valproate consistently reduced ADD throughout the treatment schedule but failed to significantly reduce SS. Lastly, ethosuximide failed to exhibit effective anticonvulsant properties. Our results indicate that the guinea-pig kindling model correctly predicted the actions of these common anticonvulsant drugs in the treatment of partial seizures. Guinea-pig amygdala kindling appears to serve as a useful and valid model for partial epilepsy.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17256170     DOI: 10.1007/s00221-006-0716-z

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  38 in total

Review 1.  New horizons in the development of antiepileptic drugs.

Authors:  Wolfgang Löscher; Dieter Schmidt
Journal:  Epilepsy Res       Date:  2002-06       Impact factor: 3.045

2.  A permanent change in brain function resulting from daily electrical stimulation.

Authors:  G V Goddard; D C McIntyre; C K Leech
Journal:  Exp Neurol       Date:  1969-11       Impact factor: 5.330

3.  Development of epileptic seizures through brain stimulation at low intensity.

Authors:  G V Goddard
Journal:  Nature       Date:  1967-06-03       Impact factor: 49.962

4.  Effects of the competitive NMDA receptor antagonist, CGP 37849, on anticonvulsant activity and adverse effects of valproate in amygdala-kindled rats.

Authors:  W Löscher; D Hönack
Journal:  Eur J Pharmacol       Date:  1993-04-06       Impact factor: 4.432

5.  Stimulation-dependent effect of antiepileptic drugs in amygdala kindled rats on both seizure score and duration of afterdischarges.

Authors:  M Voits; H H Frey
Journal:  Pharmacol Toxicol       Date:  1994-07

6.  A pharmacological study in the kindling model of epilepsy.

Authors:  T E Albertson; R M Joy; L G Stark
Journal:  Neuropharmacology       Date:  1984-10       Impact factor: 5.250

7.  Antiepileptogenic effects of conventional anticonvulsants in the kindling model of epilespy.

Authors:  J M Silver; C Shin; J O McNamara
Journal:  Ann Neurol       Date:  1991-04       Impact factor: 10.422

8.  Arrest of seizure progression during electrical kindling in guinea-pigs with prior pentylenetetrazol-induced convulsions.

Authors:  G C Teskey; P A Valentine; C Trepel
Journal:  Epilepsy Res       Date:  1996-06       Impact factor: 3.045

9.  Kindled rats are more sensitive than non-kindled rats to the behavioural effects of combined treatment with MK-801 and valproate.

Authors:  M Dziki; D Hönack; W Löscher
Journal:  Eur J Pharmacol       Date:  1992-11-10       Impact factor: 4.432

10.  The development of tolerance to the anticonvulsant effects of clonazepam, but not sodium valproate, in the amygdaloid kindled rat.

Authors:  N A Young; S J Lewis; Q L Harris; B Jarrott; F J Vajda
Journal:  Neuropharmacology       Date:  1987-11       Impact factor: 5.250

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.