Effects of folic acid and lamotrigine therapy in some rodent models of epilepsy and behaviour

Author:

Ali Atif1,Pillai K K1,Pal Shanthi N2

Affiliation:

1. Department of Pharmacology, Faculty of Pharmacy, Jamia Hamdard (Hamdard University), New Delhi-110062, India

2. World Health Organization, 1211 Geneva 27, Switzerland

Abstract

Abstract It has been suggested that a folic acid (FA) deficiency induced by antiepileptic drugs might be the basis for the neuropsychiatric toxicity associated with these drugs. In the present study, lamotrigine (LTG), one of the newer antiepileptic drugs, was evaluated for its effect on epilepsy, mood and memory in mice. Further, the effect of the addition of FA to LTG therapy was also investigated. The increasing current electroshock seizure test was used to evaluate the anticonvulsant effect of drugs, while the forced swimming test (FST) and spontaneous alternation behaviour (SAB) models were employed for assessing the effects on mood and memory, respectively. LTG exhibited a dose-dependent increase in seizure threshold, whereas FA did not have any effect. LTG did not affect, whereas FA decreased, behavioural depression in the FST in mice. Neither LTG nor FA affected memory scores in the SAB test. The combination of LTG and FA significantly reduced depression while enhancing the effects on memory and seizure threshold. The present observations have confirmed the antiepileptic action of LTG in yet another rodent model of epilepsy. Further, the results clearly demonstrate the additional benefits on epilepsy, mood and memory brought about by the inclusion of FA in the LTG regimen.

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

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2. Megaloblastic anaemia due to phenobarbitone. The convulsant action of therapeutic doses of folic acid;Chanarin;BMJ,1960

3. Antiepileptic therapy, folate deficiency and psychiatric morbidity: a general practice survey;Edeh;Epilepsia,1985

4. Folate deficiency, anticonvulsant drugs and psychiatric morbidity;Froscher;Clin. Neuropharmacol.,1995

5. Toxicity studies;Ghosh,1984

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