Clobazam and its active metabolite N-desmethylclobazam display significantly greater affinities for alpha(2)- versus alpha(1)-GABA(A)-receptor complexes.

Article Details

Citation
Copy to clipboard

Jensen HS, Nichol K, Lee D, Ebert B

Clobazam and its active metabolite N-desmethylclobazam display significantly greater affinities for alpha(2)- versus alpha(1)-GABA(A)-receptor complexes.

PLoS One. 2014 Feb 12;9(2):e88456. doi: 10.1371/journal.pone.0088456. eCollection 2014.

PubMed ID
24533090 [ View in PubMed
]
Abstract

Clobazam (CLB), a 1,5-benzodiazepine (BZD), was FDA-approved in October 2011 for the adjunctive treatment of seizures associated with Lennox-Gastaut syndrome (LGS) in patients 2 years and older. BZDs exert various CNS effects through allosteric modulation of GABAA receptors. The structurally distinct, 1,4-BZD clonazepam (CLN) is also approved to treat LGS. The precise mechanisms of action and clinical efficacy of both are unknown. Data show that the GABAA alpha(1)-subunit-selective compound zolpidem [ZOL] exhibits hypnotic/sedative effects. Conversely, data from knock-in mice carrying BZD binding site mutations suggest that the alpha(2) subunit mediates anticonvulsant effects, without sedative actions. Hence, the specific pattern of interactions across the GABAA receptor complexes of BZDs might be reflected in their clinical efficacies and adverse effect profiles. In this study, GABAA-receptor binding affinities of CLB, N-desmethylclobazam (N-CLB, the major metabolite of CLB), CLN, and ZOL were characterized with native receptors from rat-brain homogenates and on cloned receptors from HEK293 cells transfected with combinations of alpha (alpha(1), alpha(2), alpha(3), or alpha(5)), beta(2), and gamma(2) subtypes. Our results demonstrate that CLB and N-CLB have significantly greater binding affinities for alpha(2)- vs. alpha(1)-receptor complexes, a difference not observed for CLN, for which no distinction between alpha(2) and alpha(1) receptors was observed. Our experiments with ZOL confirmed the high preference for alpha(1) receptors. These results provide potential clues to a new understanding of the pharmacologic modes of action of CLB and N-CLB.

DrugBank Data that Cites this Article

Drugs