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The Journal of Neuroscience, May 15, 2000, 20(10):3571-3579
Pregnenolone Sulfate Modulates Inhibitory Synaptic Transmission
by Enhancing GABAA Receptor Desensitization
Weixing
Shen1,
Steven
Mennerick1, 3,
Douglas F.
Covey2, and
Charles F.
Zorumski1, 3
Departments of 1 Psychiatry, 2 Molecular
Biology and Pharmacology, and 3 Neurobiology, Washington
University School of Medicine, St. Louis, Missouri
We examined the effects of the neurosteroid pregnenolone sulfate
(PS) on GABAA receptor-mediated synaptic currents and
currents elicited by rapid applications of GABA onto nucleated
outside-out patches in cultured postnatal rat hippocampal neurons. At
10 µM, PS significantly depressed peak responses and
accelerated the decay of evoked inhibitory synaptic currents.
In nucleated outside-out patches, PS depressed peak currents and
speeded deactivation after 5 msec applications of a saturating concentration of GABA. PS also increased the rate and degree of macroscopic GABA receptor desensitization during prolonged GABA applications. In a paired GABA application paradigm, PS slowed the rate
of recovery from desensitization.
In contrast to its prominent effects on currents produced by saturating
GABA concentrations, PS had only small effects on peak currents and
failed to alter deactivation after brief applications of the weakly
desensitizing GABAA receptor agonists taurine and -alanine. However, when -alanine was applied for a
sufficient duration to promote receptor desensitization, PS augmented
macroscopic desensitization and slowed deactivation.
These results suggest that PS inhibits GABA-gated chloride currents by
enhancing receptor desensitization and stabilizing desensitized states.
This contention is supported by kinetic modeling studies in which
increases in the rate of entry into doubly liganded desensitized states
mimic most effects of PS.
Key words:
GABA; neurosteroids; desensitization; synapses; outside-out patches; kinetics
Copyright © 2000 Society for Neuroscience 0270-6474/00/20103571-09$05.00/0
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