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The Benzodiazepine Binding Sites of GABAA Receptors.

E. Sigel,M. Ernst

2018 · DOI: 10.1016/j.tips.2018.03.006
TIPS - Trends in Pharmacological Sciences · 263 Citations

TLDR

It is discussed here how far this separation has been achieved, and recent progress towards the discovery of novel ligands for canonical and non-canonical binding sites is outlined.

Abstract

Everyday activity is based on a subtle equilibrium of excitatory and inhibitory neuronal systems. The most prominent players in neuronal inhibition are synaptic and extrasynaptic GABAA receptors. Benzodiazepines are popular drugs that act as positive allosteric modulators of a subset of these receptors. Benzodiazepines have sedative, hypnotic, muscle-relaxant, and anticonvulsive effects, and are of outstandingly low overdose risk. The discovery of a large number of subtypes of GABAA receptors has raised hopes for a clear separation of this spectrum of actions. We discuss here how far this separation has been achieved, and outline recent progress towards the discovery of novel ligands for canonical and non-canonical binding sites.