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Calcium channel anticonvulsant drug effects

Many anticonvulsant drugs, as a major part of their mechanism of action, block the sodium channel, but other effective agents do not use this mechanism. Which of the following anticonvulsants has the ability to block T-calcium currents as its primary mechanism of action ... [Pg.383]

In cell culture preparations, diphenylhydantoin, carbamazepine and valproate have been shown to reduce membrane excitability at therapeutically relevant concentrations. This membrane-stabilizing effect is probably due to a block in the sodium channels. High concentrations of diazepam also have similar effects, and the membrane-stabilizing action correlates with the action of these anticonvulsants in inhibiting maximal electroshock seizures. Intracellular studies have shown that, in synaptosomes, most anticonvulsants inhibit calcium-dependent calmodulin protein kinase, an effect which would contribute to a reduction in neurotransmitter release. This action of anticonvulsants would appear to correlate with the potency of the drugs in inhibiting electroshock seizures. The result of all these disparate actions of anticonvulsants would be to diminish synaptic efficacy and thereby reduce seizure spread from an epileptic focus. [Pg.306]


See other pages where Calcium channel anticonvulsant drug effects is mentioned: [Pg.279]    [Pg.192]    [Pg.32]    [Pg.404]    [Pg.704]    [Pg.296]    [Pg.61]    [Pg.913]    [Pg.196]    [Pg.59]   
See also in sourсe #XX -- [ Pg.70 ]




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Anticonvulsant drugs

Anticonvulsive effect

Anticonvulsives

Calcium channels

Channel effect

Channeling effects

Channelling effects

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