The novel anticonvulsant BIA 2-093 inhibits transmitter release during opening of voltage-gated sodium channels: a comparison with carbamazepine and oxcarbazepine
- 30 April 2002
- journal article
- research article
- Published by Elsevier in Neurochemistry International
- Vol. 40 (5) , 435-440
- https://doi.org/10.1016/s0197-0186(01)00101-2
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Metabolism of two new antiepileptic drugs and their principal metabolites S(+)- and R(−)-10,11-dihydro-10-hydroxy carbamazepineEpilepsy Research, 2001
- Interaction of the Novel Anticonvulsant, BIA 2‐093, with Voltage‐Gated Sodium Channels: Comparison with CarbamazepineEpilepsia, 2001
- Inhibition of glutamate release by BIA 2-093 and BIA 2-024, two novel derivatives of carbamazepine, due to blockade of sodium but not calcium channels11Abbreviations: AED, antiepileptic drug; CBZ, carbamazepine; OXC, oxcarbazepine; and 4-AP, 4-aminopyridine.Biochemical Pharmacology, 2001
- Anticonvulsant and Sodium Channel-Blocking Properties of Novel 10,11-Dihydro-5H-dibenz[b,f]azepine-5-carboxamide DerivativesJournal of Medicinal Chemistry, 1999
- Modifications of the Brandel Superfusion 600 system and other revisions in superfusion technique improve the measurement of endogenous dopamine release in vitroJournal of Neuroscience Methods, 1996
- Rat brain neurotransmitter turnover rates altered during withdrawal from chronic cocaine administrationBrain Research, 1995
- A double-blind study comparing oxcarbazepine and carbamazepine in patients with newly diagnosed, previously untreated epilepsyEpilepsy Research, 1989
- Pharmacology of Antiepileptic DrugsEpilepsia, 1987
- Common Anticonvulsants Inhibit Ca2+ Uptake and Amino Acid Neurotransmitter Release In VitroEpilepsia, 1987
- Pharmacological Studies on Lamotrigine, A Novel Potential Antiepileptic DrugEpilepsia, 1986