Vinpocetine is as potent as phenytoin to block voltage-gated Na+ channels in rat cortical neurons
- 1 February 1995
- journal article
- research article
- Published by Elsevier in European Journal of Pharmacology
- Vol. 273 (3), 303-306
- https://doi.org/10.1016/0014-2999(94)00755-v
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Comparative study of voltage-sensitive sodium channel blockers in focal ischaemia and electric convulsions in rodentsNeuroscience Letters, 1994
- Vinpocetine preferentially antagonizes quisqualate/AMPA receptor responses: evidence from release and ligand binding studiesEuropean Journal of Pharmacology, 1991
- Vinpocetine increases the neuroprotective effect of adenosine in vitroEuropean Journal of Pharmacology, 1991
- Effects of several cerebroprotective drugs on NMDA channel function: evaluation using Xenopus oocytes and [3H]MK-801 bindingEuropean Journal of Pharmacology: Molecular Pharmacology, 1991
- Vinpocetin protects against excitotoxic cell death in primary cultures of rat cerebral cortexEuropean Journal of Pharmacology, 1990
- Lack of excitotoxic cell death in serum-free cultures of rat cerebral cortexBrain Research, 1990
- The use of Xenopus oocytes to evaluate drugs affecting brain Ca2+ channels: effects of bifemelane and several nootropic agentsEuropean Journal of Pharmacology: Molecular Pharmacology, 1990
- The Families of Cognition EnhancersPharmacopsychiatry, 1989
- A Double‐Blind Placebo Controlled Evaluation of the Safety and Efficacy of Vinpocetine in the Treatment of Patients with Chronic Vascular Senile Cerebral DysfunctionJournal of the American Geriatrics Society, 1987
- Selective inhibitors of three forms of cyclic nucleotide phosphodiesterasesTrends in Pharmacological Sciences, 1984