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Nitric oxide synthase inhibitor facilitates focal seizures induced by aminopyridine in rat.

Abstract
The effects of N-nitro-L-arginine (NA), a nitric oxide (NO) synthase inhibitor, were investigated on the focal ictal-like seizure induced by 3-aminopyridine in rat neocortex in vivo. Intraperitoneal and intracerebroventricular (i.c.v.) injections of NA markedly facilitated propagation of epileptiform events. In addition, NA injected i.c.v. increased the number/hour of individual ictal periods while decreasing their duration. In the presence of NA and an N-methyl-D-aspartate (NMDA) receptor antagonist D(-)2-amino-5-phosphonovaleric acid (APV) the number of ictal periods increased while their duration synergically decreased. APV by itself did not change the number of ictal episodes but decreased their duration. Our results suggest that NO inhibits the induction and propagation of seizure activity. We cannot distinguish the proportion of neuronal and/or vascular NO involved in our experimental conditions, but these effects seem to be independent of the NMDA receptors.
AuthorsB Boda, M Szente
JournalNeuroscience letters (Neurosci Lett) Vol. 209 Issue 1 Pg. 37-40 (May 03 1996) ISSN: 0304-3940 [Print] Ireland
PMID8734904 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Aminopyridines
  • Enzyme Inhibitors
  • Receptors, N-Methyl-D-Aspartate
  • Nitroarginine
  • 2-Amino-5-phosphonovalerate
  • Arginine
  • Nitric Oxide Synthase
Topics
  • 2-Amino-5-phosphonovalerate (pharmacology)
  • Aminopyridines
  • Animals
  • Arginine (administration & dosage, analogs & derivatives, pharmacology)
  • Cerebral Ventricles (drug effects, physiology, physiopathology)
  • Drug Synergism
  • Enzyme Inhibitors (administration & dosage, pharmacology)
  • Epilepsies, Partial (chemically induced, physiopathology)
  • Functional Laterality
  • Injections, Intraventricular
  • Nitric Oxide Synthase (antagonists & inhibitors)
  • Nitroarginine
  • Rats
  • Rats, Wistar
  • Receptors, N-Methyl-D-Aspartate (antagonists & inhibitors)
  • Seizures (chemically induced, physiopathology)

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