Cerebral Cortex Advance Access originally published online on October 12, 2005
Cerebral Cortex 2006 16(8):1134-1141; doi:10.1093/cercor/bhj055
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THIP, a Hypnotic and Antinociceptive Drug, Enhances an Extrasynaptic GABAA Receptor-mediated Conductance in Mouse Neocortex
Synaptic Physiology Laboratory, Institute of Physiology and Biophysics, University of Aarhus, DK-8000 Aarhus C, Denmark
Address correspondence to Kimmo Jensen, Institute of Physiology and Biophysics, Building 160, Room 116, Faculty of Health Sciences, University of Aarhus, DK-8000 Aarhus C, Denmark. Email: kimmo{at}fi.au.dk.
THIP (4,5,6,7-tetrahydroisoxazolo[5,4-c]pyridin-3-ol) is a selective GABAA receptor agonist with a preference for
-subunit containing GABAA receptors. THIP is currently being tested in human trials for its hypnotic effects, displaying advantageous tolerance and addiction properties. Since its cellular actions in the neocortex are uncertain, we studied the effects of THIP on neurons in slices of frontoparietal neocortex of 13- to 19-day-old (P1319) mice. Using whole-cell patch-clamp recordings, we found that the clinically relevant THIP concentration of 1 µM induced a robust tonic GABAA-mediated current in layer 2/3 neurons. In comparison, only a minute tonic current was induced by mimicking in vivo endogenous GABA levels. Miniature IPSCs were not affected by 1 µM THIP suggesting an extrasynaptic site of action. The EC50 for THIP was 44 µM. In accordance with the stronger expression of
-containing receptors in superficial neocortical layers, THIP induced a 44% larger tonic current in layer 2/3 than in layer 5 neurons. Finally, monitoring spontaneously active neocortical neurons, THIP caused an overall depression of inhibitory activity, while enhancing excitatory activity prominently. Our studies suggest that THIP activates an extrasynaptic GABAA receptor-mediated conductance in the neocortex, which may alter the cortical network activity.
Key Words:
-subunit extrasynaptic receptors GABA mouse neocortex THIP
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