Mechanisms of action of carbamazepine and its derivatives, oxcarbazepine, BIA 2-093, and BIA 2-024

• Published in: Neurochemical research Vol. 27; no. 1-2; pp. 121 - 130
• Main Authors: AMBROSIO, Antonio F, SOARES-DA-SILVA, Patricio, CARVALHO, Caetana M, CARVALHO, Arsélio P
• Format: Journal Article
• Language: English
• Published: New York, NY Springer 01.02.2002; Springer Nature B.V
• Subjects: Animals; Anticonvulsants - chemistry; Anticonvulsants - therapeutic use; Biological and medical sciences; Carbamazepine - analogs & derivatives; Carbamazepine - chemistry; Carbamazepine - therapeutic use; Dibenzazepines - therapeutic use; Epilepsy - drug therapy; Humans; Oxcarbazepine; Sodium Channel Blockers - therapeutic use
• ISSN: 0364-3190; 1573-6903
• DOI: 10.1023/A:1014814924965

Carbamazepine (CBZ) has been extensively used in the treatment of epilepsy, as well as in the treatment of neuropathic pain and affective disorders. However, the mechanisms of action of this drug are not completely elucidated and are still a matter of debate. Since CBZ is not very effective in some epileptic patients and may cause several adverse effects, several antiepileptic drugs have been developed by structural variation of CBZ, such as oxcarbazepine (OXC), which is used in the treatment of epilepsy since 1990. (S)-(-)-10-acetoxy-10,11-dihydro-5H-dibenz [b,f]azepine-5-carboxamide (BIA 2-093) and 10,11-dihydro-10-hydroxyimino-5H-dibenz[b,f] azepine-5-carboxamide (BIA 2-024), which were recently developed by BIAL, are new putative antiepileptic drugs, with some improved properties. In this review, we will focus on the mechanisms of action of CBZ and its derivatives, OXC, BIA 2-093 and BIA 2-024. The available data indicate that the anticonvulsant efficacy of these AEDs is mainly due to the inhibition of sodium channel activity.