The broad-spectrum activity of perampanel: state of the art and future perspective of AMPA antagonism beyond epilepsy
- PMID: 37483446
- PMCID: PMC10359664
- DOI: 10.3389/fneur.2023.1182304
The broad-spectrum activity of perampanel: state of the art and future perspective of AMPA antagonism beyond epilepsy
Abstract
Glutamate is the brain's main excitatory neurotransmitter. Glutamatergic neurons primarily compose basic neuronal networks, especially in the cortex. An imbalance of excitatory and inhibitory activities may result in epilepsy or other neurological and psychiatric conditions. Among glutamate receptors, AMPA receptors are the predominant mediator of glutamate-induced excitatory neurotransmission and dictate synaptic efficiency and plasticity by their numbers and/or properties. Therefore, they appear to be a major drug target for modulating several brain functions. Perampanel (PER) is a highly selective, noncompetitive AMPA antagonist approved in several countries worldwide for treating different types of seizures in various epileptic conditions. However, recent data show that PER can potentially address many other conditions within epilepsy and beyond. From this perspective, this review aims to examine the new preclinical and clinical studies-especially those produced from 2017 onwards-on AMPA antagonism and PER in conditions such as mesial temporal lobe epilepsy, idiopathic and genetic generalized epilepsy, brain tumor-related epilepsy, status epilepticus, rare epileptic syndromes, stroke, sleep, epilepsy-related migraine, cognitive impairment, autism, dementia, and other neurodegenerative diseases, as well as provide suggestions on future research agenda aimed at probing the possibility of treating these conditions with PER and/or other AMPA receptor antagonists.
Keywords: AMPA antagonists; AMPA receptors; epilepsy; glutamate; migraine; perampanel; sleep.
Copyright © 2023 Perversi, Costa, Labate, Lattanzi, Liguori, Maschio, Meletti, Nobili, Operto, Romigi, Russo and Di Bonaventura.
Conflict of interest statement
CC has received research support, speaker honoraria, and travel expenses from Bial, Eisai Europe Limited, GW Pharma, Lusopharma, PIAM Pharma, and UCB Pharma. CB has received consulting fees or speaker honoraria from UCB Pharma, Eisai, GW Pharmaceuticals, Bial, and Lusopharma. AL has received consulting fees or speaker honoraria from UCB Pharma, Eisai, GW Pharmaceuticals, Bial, and Lusopharma. SL has received speaker or consultancy fees from Angelini Pharma, Eisai, GW Pharmaceuticals, and UCB Pharma, and has served on Angelini Pharma, Arvelle Therapeutics, BIAL, EISAI, and GW Pharmaceuticals advisory boards. SM has received speaker or consultancy fees from Eisai, GW Pharmaceuticals, and UCB Pharma and has served on advisory boards for Eisai, UCB and GW Pharmaceuticals. LN has received speaker or consultancy fees from Fidia Pharma, Eisai, and Roche. FO has received speaker or consultancy fees from Eisai, GW Pharmaceuticals, and Angelini Pharma; FP is a collaborator of Polistudium SRL and was compensated for medical writing in accordance with the Good Publication Practice 2022. AR has received consulting fees or speaker honoraria from Angelini Pharma, EISAI, Jazz, and Bioprojet. ER has received speaker fees or funding and has participated in advisory boards for Arvelle Therapeutics, Angelini, Eisai, Kolfarma, JAZZ pharmaceuticals, Pfizer, GW Pharmaceuticals, UCB, and Lundbeck. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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