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PMID: 2054668 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Electrophysiological evidence for a rapid membrane action of the gonadal steroid, 17 beta-estradiol, on CA1 pyramidal neurons of the rat hippocampus.

Brain research ·Vol. 543 ·No. 1 ·1991-03-08 ·Pages 148-52

Wong M, Moss RL

Abstract

The rapid electrophysiological effects of 17 beta-estradiol on CA1 pyramidal neurons (n = 86) were investigated utilizing intracellular recording from the rat hippocampal slice preparation. Bath application of 17 beta-estradiol, but not 17 alpha-estradiol, caused a reversible depolarization and increased input resistance with a latency of less than 1 min in 19.8% of CA1 neurons tested. There was no significant difference in the percentage of estradiol-responsive cells between male and female rats. Estradiol-responsive cells were identified from prepubertal female rats, as well as females in all stages of the estrous cycle. 17 beta-estradiol had no effect on the slow afterhyperpolarization or accommodative properties of CA1 neurons. In 2 out of 4 cells tested, the specific antiestrogen, tamoxifen, blocked the excitatory response to 17 beta-estradiol.

MeSH Terms
Animals Diestrus/physiology Estradiol/pharmacology Estrus/physiology Female Hippocampus/physiology In Vitro Techniques Male Membrane Potentials/drug effects Neurons/drug effects,physiology Proestrus/physiology Pyramidal Tracts/drug effects,physiology Rats Rats, Inbred Strains Sexual Maturation Tamoxifen/pharmacology
Chemicals
Tamoxifen Estradiol
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Wong M
Department of Physiology, University of Texas Southwestern Medical Center, Dallas 75235.
Moss R L
Article Info
Journal
Brain research
Abbr.
Brain Res
ISSN
0006-8993
Published
1991-03-08
Pages
148-52
Language
English
Region
Netherlands
NLM ID
0045503
Subset
IM
Grants
NIGMS NIH HHS · GM08014 · United States
NICHD NIH HHS · HD09988 · United States
NIMH NIH HHS · MH44591 · United States
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