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The antimyoclonic action of clonazepam through a GABA--independent mechanism.

Abstract
The present study investigates whether clonazepam exerts its antimyoclonic action through a GABA independent mechanism. We have studied the antimyoclonic effect of clonazepam and compared it with that of aminooxyacetic acid (AOAA), a GABA transaminase inhibitor, against myoclonus induced by picrotoxin, a GABA receptor antagonist and allylglycine, a drug which inhibits synthesis and release of GABA. We have also investigated the effect of clonazepam against picrotoxin-induced myoclonus in rats pretreated with either AOAA or submyoclonic dose of allylgylycine. Clonazepam pretreatment inhibited both picrotoxin and allylglycine-induced myoelonus whereas AOAA was effective in inhibiting only picrotoxin-induced myoclonus. The protective effect of clonazepam against picrotoxin-induced myoclonus was potentiated by AOAA pretreatment. Moreover, clonazepam afforded protection against picrotoxin-induced myoclonus in rats pretreated with a submyoclonic GABA reducing dose of allylglycine. These findings indicate that a GABA independent mechanism may also be involved in the antimyoclonic action of clonazepam.
AuthorsV Paul, M S Krishnamoorthy
JournalIndian journal of physiology and pharmacology (Indian J Physiol Pharmacol) 1989 Oct-Dec Vol. 33 Issue 4 Pg. 243-6 ISSN: 0019-5499 [Print] India
PMID2620967 (Publication Type: Journal Article)
Chemical References
  • Anticonvulsants
  • Allylglycine
  • Picrotoxin
  • Aminooxyacetic Acid
  • gamma-Aminobutyric Acid
  • Clonazepam
  • 4-Aminobutyrate Transaminase
Topics
  • 4-Aminobutyrate Transaminase (metabolism)
  • Allylglycine
  • Aminooxyacetic Acid
  • Animals
  • Anticonvulsants
  • Brain Chemistry (drug effects)
  • Clonazepam (pharmacology)
  • Male
  • Myoclonus (chemically induced, drug therapy)
  • Picrotoxin
  • Rats
  • Rats, Inbred Strains
  • gamma-Aminobutyric Acid (metabolism, physiology)

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