The GABA-A beta3 subunit mediates
anaesthesia induced by etomidate
by
O'Meara GF, Newman RJ, Fradley RL,
Dawson GR, Reynolds DS.
Merck Sharp & Dohme Research Laboratories,
The Neuroscience Research Centre,
Terlings Park, Harlow, Essex CM20 2QR, UK.
Neuroreport. 2004 Jul 19;15(10):1653-1656

ABSTRACT

GThe i.v. agent etomidate exerts its anaesthetic actions through potentiation of gamma-aminobutyric acid-A receptors containing beta2 and beta3 subunits. It was recently shown that the beta2 subunit contributes to the sedative properties of etomidate, whereas the beta3 subunit is responsible for its anaesthetic properties. However, these studies evaluated anaesthetic effects in point mutation mice in which the effect of etomidate was decreased, but not abolished, at the beta2 subunit. Here we have used beta2 knockout mice to completely remove any contribution of the beta2 subunit to the effects of etomidate. Etomidate was equally anaesthetic in wildtype and knockout mice, thus further confirming that efficacy at the beta3 subunit only is sufficient to induce general anaesthesia.

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