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Functional characterization of the antiepileptic drug candidate, padsevonil, on GABA A receptors
Author(s) -
Niespodziany Isabelle,
Ghisdal Philippe,
Mullier Brice,
Wood Martyn,
Provins Laurent,
Kaminski Rafal M.,
Wolff Christian
Publication year - 2020
Publication title -
epilepsia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.687
H-Index - 191
eISSN - 1528-1167
pISSN - 0013-9580
DOI - 10.1111/epi.16497
Subject(s) - gabaa receptor , agonist , pharmacology , postsynaptic potential , gabaa rho receptor , chemistry , receptor , gamma aminobutyric acid , chlordiazepoxide , benzodiazepine , biology , biochemistry , diazepam
Objective The antiepileptic drug candidate, padsevonil, is the first in a novel class of drugs designed to interact with both presynaptic and postsynaptic therapeutic targets: synaptic vesicle 2 proteins and γ‐aminobutyric acid type A receptors (GABA A Rs), respectively. Functional aspects of padsevonil at the postsynaptic target, GABA A Rs, were characterized in experiments reported here. Methods The effect of padsevonil on GABA‐mediated Cl − currents was determined by patch clamp on recombinant human GABA A Rs (α1β2γ2) stably expressed in a CHO‐K1 cell line and on native GABA A Rs in cultured rat primary cortical neurons. Padsevonil selectivity for GABA A R subtypes was evaluated using a two‐electrode voltage clamp on recombinant human GABA A Rs (α1‐5/β2/γ2) in Xenopus oocytes. Results In recombinant GABA A Rs, padsevonil did not evoke Cl − currents in the absence of the agonist GABA. However, when co‐administered with GABA at effective concentration (EC) 20 , padsevonil potentiated GABA responses by 167% (EC 50 138 nmol/L) and demonstrated a relative efficacy of 41% compared with zolpidem, a reference benzodiazepine site agonist. Similarly, padsevonil demonstrated GABA‐potentiating activity at native GABA A Rs (EC 50 208 nmol/L) in cultured rat cortical neurons. Padsevonil also potentiated GABA (EC 20 ) responses in GABA A Rs expressed in oocytes, with higher potency at α1‐ and α5‐containing receptors (EC 50 295 and 281 nmol/L) than at α2‐ and α3‐containing receptors (EC 50 1737 and 2089 nmol/L). Compared with chlordiazepoxide—a nonselective, full GABA A R agonist—the relative efficacy of padsevonil was 60% for α1β2γ2, 26% for α2β2γ2, 56% for α3β2γ2, and 41% for α5β2γ2; no activity was observed at benzodiazepine‐insensitive α4β2γ2 receptors. Significance Results of functional investigations on recombinant and native neuronal GABA A Rs show that padsevonil acts as a positive allosteric modulator of these receptors, with a partial agonist profile at the benzodiazepine site. These properties may confer better tolerability and lower potential for tolerance development compared with classic benzodiazepines currently used in the clinic.