Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 98, Issue 13, Pages 7093-7100Publisher
NATL ACAD SCIENCES
DOI: 10.1073/pnas.121146898
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- NIA NIH HHS [P01AG16765, P01 AG016765] Funding Source: Medline
- NINDS NIH HHS [NS070880] Funding Source: Medline
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Estrogens (E) and progestins regulate synaptogenesis in the CA1 region of the dorsal hippocampus during the estrous cycle of the female rat, and the functional consequences include changes in neurotransmission and memory. Synapse formation has been demonstrated by using the Golgi technique, dye filling of cells, electron microscopy. and radioimmunocytochemistry. N-methyl-D-aspartate (NMDA) receptor activation is required, and inhibitory interneurons play a pivotal role as they express nuclear estrogen receptor alpha (ER alpha) and show E-induced decreases of GABAergic activity. Although global decreases in inhibitory tone may be important, a more local role for E in CA1 neurons seems likely. The rat hippocampus expresses both ER alpha and ER beta mRNA. At the light microscopic level, autoradiography shows cell nuclear [H-3]estrogen and [I-125]estrogen uptake according to a distribution that primarily reflects the localization of ER alpha -immunoreactive interneurons in the hippocampus. However, recent ultrastructural studies have revealed extranuclear ERa immunoreactivity (IR) within select dendritic spines on hippocampal principal cells, axon terminals, end glial processes, localizations that would not be detectable by using standard light microscopic methods. Based on recent studies showing that both types of ER are expressed in a form that activates second messenger systems, these findings support a testable model in which local, non-genomic regulation by estrogen participates along with genomic actions of estrogens in the regulation of synapse formation.
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