Abstract
Tonic inhibition mediated by extrasynaptic GABAA receptors (GABARs) sensing ambient levels of GABA can profoundly alter the membrane input resistance to affect cellular excitability. Therefore, regulation of tonic inhibition is an attractive mechanism to control the levels of cortical firing. In cortical pyramidal cells, tonic inhibition is regulated by age and several neurotransmitters and is affected by stroke and epilepsy. However, the possible role of sensory experience has not been examined. Here, we report that a brief 2-day exposure to dark reduces by 1/3 the inhibitory tonic conductance recorded in layer II/III pyramidal cells of the mouse juvenile (postnatal day 12–27) visual cortex. In these cells, tonic inhibition is carried primarily by GABARs containing the δ subunit. Consistently, the dark exposure reduction in conductance was associated with a reduction in δ subunit levels, which were not affected in control frontal cortex. We propose that a deprivation-induced reduction in tonic inhibition might serve a homeostatic function by increasing the firing levels of cells in deprived cortical circuits.
SIGNIFICANCE STATEMENT Previous in vivo studies reported rapid increases in spontaneous activity after visual deprivation. These adaptive responses to deprivation are believed to reflect a reduction in the recruitment of inhibitory circuits. Notably, the possible role of tonic GABAergic inhibition, which strongly limits cellular and network excitability, has not been examined. We report that a brief 2-day exposure to dark reduces both the conductance of tonic inhibition in layer 2/3 pyramidal cells and the expression of receptors containing the δ-GABAA receptor subunit, the principal carrier of tonic inhibition in these cells. These results suggest that the early phases of homeostatic adaptations to sensory deprivation might result from modulation of GABAergic function at multiple levels.