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The FASEB Journal Express Article doi:10.1096/fj.02-0611fje
Published online December 3, 2002

General anesthetic actions in vivo strongly attenuated by a point mutation in the GABAA receptor β3 subunit

Rachel Jurd, Margarete Arras, Sachar Lambert, Berthold Drexler, Roberta Siegwart, Florence Crestani, Michael Zaugg, Kaspar E. Vogt, Birgit Ledermann, Bernd Antkowiak, and Uwe Rudolph

E-mail contact: rudolph{at}pharma.unizh.ch

General anesthetics are widely used in clinical practice. On the molecular level, these compounds have been shown to modulate the activity of various neuronal ion channels. However, the functional relevance of identified sites in mediating essential components of the general anesthetic state, such as immobility and hypnosis, is still unknown. Using gene-targeting technology, we generated mice harboring a subtle point mutation (N265M) in the second transmembrane region of the β3 subunit of the GABAA receptor. In these mice, the suppression of noxious-evoked movements in response to the intravenous anesthetics etomidate and propofol is completely abolished, while only slightly decreased with the volatile anesthetics enflurane and halothane. β3(N265M) mice also display a profound reduction in the loss of righting reflex duration in response to intravenous but not volatile anesthetics. In addition, electrophysiological recordings revealed that anesthetic agents were significantly less effective in enhancing GABAA receptor-mediated currents, and in decreasing spontaneous action potential firing in cortical brain slices derived from mutant mice. Taken together, our results demonstrate that a single molecular target, and indeed a specific residue (N265) located within the GABAA receptor β3 subunit, is a major determinant of behavioral responses evoked by the intravenous anesthetics etomidate and propofol, whereas volatile anesthetics appear to act via a broader spectrum of molecular targets.

Key words: anesthesia · animal model · knock-in · gene targeting




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