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Effect of Carbamazepine and Lamotrigine on Cognitive Function and Oxidative Stress in Brain during Chemical Epileptogenesis in Rats
Author(s) -
Arora Tarun,
Mehta Ashish K.,
Sharma Krishna K.,
Mediratta Pramod K.,
Banerjee Basu D.,
Garg Gobind R.,
Sharma Amit K.
Publication year - 2010
Publication title -
basic and clinical pharmacology and toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.805
H-Index - 90
eISSN - 1742-7843
pISSN - 1742-7835
DOI - 10.1111/j.1742-7843.2009.00499.x
Subject(s) - lamotrigine , carbamazepine , oxidative stress , epileptogenesis , malondialdehyde , anticonvulsant , pharmacology , chemistry , glutathione , epilepsy , anesthesia , psychology , endocrinology , medicine , hippocampus , biochemistry , neuroscience , enzyme
The present study assessed the effect of carbamazepine and lamotrigine on cognitive function and oxidative stress in brain during chemically induced epileptogenesis in rats. Epileptogenesis was induced by administration of pentylenetetrazole (30 mg/kg, s.c.) on alternate days (three times/week) for 9–11 weeks or until stage 4 of seizure score was achieved. The neurobehavioural parameters used for cognitive assessment were step‐down latency in continuous avoidance apparatus and transfer latency in elevated plus maze test paradigm. Carbamazepine and lamotrigine were administered intraperitoneally in doses of 60 mg/kg and 25 mg/kg, respectively, according to the groups, once a day for 11 weeks. Oxidative stress was assessed in isolated homogenized whole brain samples and estimated for the levels of malondialdehyde, reduced glutathione, catalase and superoxide dismutase. The results showed that lamotrigine did not produce any change in cognitive function, while carbamazepine produced cognitive dysfunction. Cognitive decline seen in the carbamazepine‐treated pentylenetetrazole‐kindled group was also associated with increased oxidative stress. Lamotrigine treatment had no effect on oxidative stress parameters alone, while it significantly decreased oxidative stress in the pentylenetetrazole‐kindled group as compared to the pentylenetetrazole‐kindled carbamazepine‐treated group.