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The Journal of Neurophysiology Vol. 81 No. 2 February 1999, pp. 925-929
Copyright ©1999 by the American Physiological Society
RAPID COMMUNICATION
-Estradiol Enhances NMDA Receptor-Mediated EPSPs and
Long-Term Potentiation
1Department of Psychology, Loyola Marymount University, Los Angeles, California 90045; 2Program in Neuroscience, University of Southern California, Los Angeles, California 90089; and 3Department of Molecular Pharmacology and Toxicology, University of Southern California, Los Angeles, California 90033
17
-estradiol enhances NMDA receptor-mediated EPSPs and long-term
potentiation. Gonadal steroid hormones influence CNS
functioning through a variety of different mechanisms. To test the
hypothesis that estrogen modulates synaptic plasticity in the
hippocampus, in vitro hippocampal slices from 2-mo-old Sprague-Dawley
male rats were used to determine the effect of 17
-estradiol on both N-methyl-D-aspartate (NMDA) receptor-mediated
excitatory postsynaptic potentials (EPSPs) through intracellular
recordings and long-term potentiation (LTP) through extracellular
recordings. Intracellular EPSPs and extracellular field EPSPs (fEPSPs)
were recorded from CA1 pyramidal cells by stimulating Schaffer
collateral fibers. In intracellular experiments, slices were perfused
with medium containing bicuculline (5 µM) and low Mg2+
(0.1 mM) to enhance the NMDA receptor-mediated currents and
6,7-dinitroquinoxaline-2,3-dione (DNQX) (10 µM) to block the
-amino-3-hydroxy-5-methyl-4-isoxazoleproprianate (AMPA)
receptor-mediated component. The effects of 17
-estradiol on NMDA
receptor-mediated activity were excitatory; concentrations >10 nM
induced seizure activity, and lower concentrations (1 nM) markedly
increased the amplitude of NMDA-mediated EPSPs (both the first and
second responses increased during paired pulse stimulation by 180 and
197%, respectively). In extracellular experiments, slices perfused
with 17
-estradiol (100 pM) exhibited a pronounced, persisting, and
significant enhancement of LTP of both the fEPSP slope (192%) and
fEPSP amplitude (177%) compared with control slices (fEPSP slope = 155%; fEPSP amplitude = 156%) 30 min after high-frequency
stimulation. These data demonstrate that estrogen enhances NMDA
receptor-mediated currents and promotes an enhancement of LTP
magnitude.
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