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The anti‐seizure drugs vinpocetine and carbamazepine, but not valproic acid, reduce inflammatory IL ‐1β and TNF ‐α expression in rat hippocampus
Author(s) -
Gómez Carlos D.,
Buijs Rudolf M.,
Sitges María
Publication year - 2014
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/jnc.12784
Subject(s) - carbamazepine , vinpocetine , valproic acid , pharmacology , pentylenetetrazol , anticonvulsant , pilocarpine , chemistry , epilepsy , cytokine , proinflammatory cytokine , inflammation , medicine , immunology , psychiatry
In the present study, the effects of the two classical anti‐epileptic drugs, carbamazepine and valproic acid, and the non‐classical anti‐seizure drug vinpocetine were investigated on the expression of the pro‐inflammatory cytokines IL ‐1β and TNF ‐α in the hippocampus of rats by PCR or western blot after the administration of one or seven doses. Next, the effects of the anti‐seizure drugs were investigated on the rise in cytokine expression induced by lipopolysaccharides ( LPS ) inoculation in vivo . To validate our methods, the changes induced by the pro‐convulsive agents 4‐aminopyridine, pentylenetetrazole and pilocarpine were also tested. Finally, the effect of the anti‐seizure drugs on seizures and on the concomitant rise in pro‐inflammatory cytokine expression induced by 4‐aminopyridine was explored. Results show that vinpocetine and carbamazepine reduced the expression of IL ‐1β and TNF ‐α from basal conditions, and the increase in both pro‐inflammatory cytokines induced by LPS . In contrast, valproic acid failed to reduce both the expression of the cytokines from basal conditions and the rise in IL ‐1β and TNF ‐α expression induced by LPS . Tonic‐clonic seizures induced either by 4‐aminopyridine, pentylenetetrazole or pilocarpine increased the expression of IL ‐1β and TNF ‐α markedly. 4‐aminopyridine‐induced changes were reduced by all the tested anti‐seizure drugs, although valproic acid was less effective. We conclude that the anti‐seizure drugs, vinpocetine and carbamazepine, whose mechanisms of action involve a decrease in ion channels permeability, also reduce cerebral inflammation.The mechanism of action of anti‐seizure drugs like vinpocetine and carbamazepine involves a decrease in Na + channels permeability. We here propose that this mechanism of action also involves a decrease in cerebral inflammation.