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The Journal of Neuroscience, March 1, 2002, 22(5):1541-1549

Enhanced Neurosteroid Potentiation of Ternary GABAA Receptors Containing the delta  Subunit

Kai M. Wohlfarth1, Matt T. Bianchi2, and Robert L. Macdonald3, 4, 5

Department of 1  Neurology and 2  Neuroscience Graduate Program, University of Michigan, Ann Arbor, Michigan 48104-1687, and Departments of 3  Neurology, 4  Molecular Physiology and Biophysics, and 5  Pharmacology, Vanderbilt University, Nashville, Tennessee 37212

Attenuated behavioral sensitivity to neurosteroids has been reported for mice deficient in the GABAA receptor delta  subunit. We therefore investigated potential subunit-specific neurosteroid pharmacology of the following GABAA receptor isoforms in a transient expression system: alpha 1beta 3gamma 2L, alpha 1beta 3delta , alpha 6beta 3gamma 2L, and alpha 6beta 3delta . Potentiation of submaximal GABAA receptor currents by the neurosteroid tetrahydrodeoxycorticosterone (THDOC) was greatest for the alpha 1beta 3delta isoform. Whole-cell GABA concentration-response curves performed with and without low concentrations (30 nM) of THDOC revealed enhanced peak GABAA receptor currents for isoforms tested without affecting the GABA EC50. alpha 1beta 3delta currents were enhanced the most (>150%), whereas the other isoform currents were enhanced 15-50%. At a higher concentration (1 µM), THDOC decreased peak alpha 1beta 3gamma 2L receptor current amplitude evoked by GABA (1 mM) concentration jumps and prolonged deactivation but had little effect on the rate or extent of apparent desensitization. Thus the polarity of THDOC modulation depended on GABA concentration for alpha 1beta 3gamma 2L GABAA receptors. However, the same protocol applied to alpha 1beta 3delta receptors resulted in peak current enhancement by THDOC of >800% and prolonged deactivation. Interestingly, THDOC induced pronounced desensitization in the minimally desensitizing alpha 1beta 3delta receptors. Single channel recordings obtained from alpha 1beta 3delta receptors indicated that THDOC increased the channel opening duration, including the introduction of an additional longer duration open state. Our results suggest that the GABAA receptor delta  subunit confers increased sensitivity to neurosteroid modulation and that the intrinsic gating and desensitization kinetics of alpha 1beta 3delta GABAA receptors are altered by THDOC.

Key words: GABAA receptor; delta subunit; neurosteroid; desensitization; single channel; gating


Copyright © 2002 Society for Neuroscience  0270-6474/02/2251541-09$05.00/0


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