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Brain Region‐Dependent Sensitivity of GABA A Receptor‐Mediated Responses to Modulation by Ethanol
Author(s) -
Proctor William R.,
Allan Andrea M.,
Dunwiddie Thomas V.
Publication year - 1992
Publication title -
alcoholism: clinical and experimental research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.267
H-Index - 153
eISSN - 1530-0277
pISSN - 0145-6008
DOI - 10.1111/j.1530-0277.1992.tb01405.x
Subject(s) - depolarization , hyperpolarization (physics) , chemistry , neuroscience , nmda receptor , electrophysiology , membrane potential , gabaa receptor , excitatory postsynaptic potential , cerebellum , hippocampal formation , biophysics , population , reversal potential , cerebral cortex , medicine , inhibitory postsynaptic potential , endocrinology , receptor , biology , patch clamp , biochemistry , environmental health , nuclear magnetic resonance spectroscopy , organic chemistry
Simultaneous extracellular and intracellular electrophysiological recordings were made from the CA1 region of rat hippocampal brain slices during superfusion with ethanol. Ethanol (80 mM) had a biphasic effect on the extracellularly recorded population spike, with an initial increase followed by a significant reduction (38%) in this response, which was maximal 10 to 15 min after the start of ethanol application. Concurrent intracellular recordings in the CA1 showed small (0.7 mV) hyperpolarization of the resting membrane potential, with no significant change in the input impedance, EPSP, GABA A and GABA B IPSPs, or after hyperpolarization (AHP) following depolarizing current injection. Ethanol reduced the amplitude and duration of depolarizing responses to brief, localized pressure‐ejection of N ‐methyl‐D‐aspartate (NMDA) onto pyramidal neuron dendrites, but did not affect the GABA A receptor‐mediated depolarizing responses to the dendritic application of GABA. In parallel studies, the effect of ethanol on GABA‐stimulated 36 Cl − flux was measured in microsac preparations from rat hippocampus, cerebellum, and cerebral cortex. Ethanol application caused substantial enhancement of the chloride uptake from cerebellar and cerebral cortical microsacs, but had no effect on 36 Cl − influx in hippocampel microsacs. These results suggest that there are important brain region‐dependent differences in the sensitivity of the GABA A receptor/chloride channel to modulation by ethanol.