Back to Search Start Over

Serotonin receptors in epilepsy: Novel treatment targets?

Authors :
Sourbron J
Lagae L
Source :
Epilepsia open [Epilepsia Open] 2022 Jun; Vol. 7 (2), pp. 231-246. Date of Electronic Publication: 2022 Feb 02.
Publication Year :
2022

Abstract

Despite the availability of over 30 antiseizure medications (ASMs), there is no "one size fits it all," so there is a continuing search for novel ASMs. There are divergent data demonstrating that modulation of distinct serotonin (5-hydroxytryptamine, 5-HT) receptors subtypes could be beneficial in the treatment of epilepsy and its comorbidities, whereas only a few ASM, such as fenfluramine (FA), act via 5-HT. There are 14 different 5-HT receptor subtypes, and most epilepsy studies focus on one or a few of these subtypes, using different animal models and different ligands. We reviewed the available evidence of each 5-HT receptor subtype using MEDLINE up to July 2021. Our search included medical subject heading (MeSH) and free terms of each "5-HT subtype" separately and its relation to "epilepsy or seizures." Most research underlines the antiseizure activity of 5-HT <subscript>1A,1D,2A,2C,3</subscript> agonism and 5-HT <subscript>6</subscript> antagonism. Consistently, FA, which has recently been approved for the treatment of seizures in Dravet syndrome, is an agonist of 5-HT <subscript>1D,2A,2C</subscript> receptors. Even though each study focused on a distinct seizure/epilepsy type and generalization of different findings could lead to false interpretations, we believe that the available preclinical and clinical studies emphasize the role of serotonergic modulation, especially stimulation, as a promising avenue in epilepsy treatment.<br /> (© 2022 The Authors. Epilepsia Open published by Wiley Periodicals LLC on behalf of International League Against Epilepsy.)

Details

Language :
English
ISSN :
2470-9239
Volume :
7
Issue :
2
Database :
MEDLINE
Journal :
Epilepsia open
Publication Type :
Academic Journal
Accession number :
35075810
Full Text :
https://doi.org/10.1002/epi4.12580