Layer-specific noradrenergic modulation of inhibition in cortical layer II/III
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Norepinephrine (NE) is released in the neocortex after activation of the locus coeruleus of the brain stem in response to novel, salient, or fight-or-flight stimuli. The role of adrenergic modulation in sensory cortices is not completely understood. We investigated the possibility that NE modifies the balance of inhibition acting on 2 different γ-aminobutyric acid (GABA)ergic pathways. Using patchclamp recordings, we found that the application of NE induces an α1 adrenergic receptor-mediated decrease of the amplitude of inhibitory postsynaptic currents (IPSCs) evoked by stimulation of layer I (LI-eIPSCs) and a β and α2 receptor-mediated increase in the amplitude of IPSCs evoked by stimulation of layer II/III (LII/III-eIPSCs). Analysis of minimal stimulation IPSCs, IPSC kinetics, and sensitivity to the GABAA receptor subunit-selective enhancer zolpidem corroborated the functional difference between LI- and LII/III-eIPSCs, suggestive of a distal versus somatic origin of LI- and LII/III-eIPSCs, respectively. These findings suggest that NE shifts the balance between distal and somatic inhibition to the advantage of the latter. We speculate that such shift modifies the balance of sensory-specific and emotional information in the integration of neural input to the upper layers of the auditory cortex. © The Author 2010. Published by Oxford University Press.
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Auditory cortex; Cortical circuitry; Dendritic inhibition; Norepinephrine; Patch clamp; Somatic inhibition 4 aminobutyric acid; 4 aminobutyric acid A receptor; zolpidem; animal experiment; animal tissue; article; auditory cortex; brain cortex; brain depth stimulation; brain electrophysiology; controlled study; inhibitory postsynaptic potential; nonhuman; noradrenergic system; patch clamp; priority journal; rat; Animals; Cerebral Cortex; gamma-Aminobutyric Acid; Neural Inhibition; Neurons; Norepinephrine; Organ Culture Techniques; Rats; Rats, Sprague-Dawley; Synapses
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