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J Neurophysiol 101: 2974-2983, 2009. First published March 25, 2009; doi:10.1152/jn.91001.2008
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GABAC Receptor-Mediated Inhibition Is Altered But Not Eliminated in the Superior Colliculus of GABAC {rho}1 Knockout Mice

Katja Schlicker1, Maureen A. McCall2 and Matthias Schmidt1

1Allgemeine Zoologie and Neurobiologie, Ruhr-Universität Bochum, Bochum, Germany; and 2Department of Ophthalmology and Visual Sciences and Psychological and Brain Sciences, University of Louisville, Louisville, Kentucky

Submitted 5 September 2008; accepted in final form 18 March 2009

GABAC receptors (GABACRs) are widely expressed in the mammalian subcortical visual system, particularly in the retina and superior colliculus (SC). GABACRs are composed of specific {rho}1–3 subunits the expression of which varies among visual structures. Thus {rho}1 subunits are most abundant in retina, and their loss eliminates GABACR expression and function. In the SC, {rho}2 subunit expression may be equal to or stronger than {rho}1 subunit expression; however, results across studies vary considerably. To more directly assess the expression of GABACR subunits, we characterized inhibition in the SC of wild-type (WT) and GABAC {rho}1 Null mice that lack expression of GABAC {rho}1 subunits. We used whole cell patch-clamp recordings and evaluated GABACR-mediated modulation of electrically evoked post synaptic currents using either agonists or antagonists in WT mice. In GABAC {rho}1 Null stratum griseum superficiale (SGS) cells, inhibitory postsynaptic currents were shorter in duration and their excitatory postsynaptic currents (EPSCs) were longer, indicating that a slow GABACR-mediated inhibitory component was reduced in each case. In contrast to retina, GABACR-mediated currents in the SC were altered but not eliminated in GABAC {rho}1 Null mice. In the majority of SC cells in GABAC {rho}1 Null mice, GABACR activation could still be induced to alter EPSC peak amplitudes in putative interneurons and in many projection neurons. These results, compared with previously published data, indicate a fundamental difference between retina and SC in the control of GABACR expression and subunit composition.


Address for reprint requests and other correspondence: M. Schmidt, Allgemeine Zoologie and Neurobiologie, Ruhr-Universität Bochum, MA 4/56, D-44780 Bochum, Germany (E-mail: Matthias.Schmidt{at}rub.de) or M. A. McCall, Dept. of Ophthalmology & Visual Sciences, University of Louisville, Louisville, KY 40202 (E-mail: ma.mccall{at}louisville.edu)







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