Abstract
Having used the cingulate cortex to demonstrate the validity of our methods for detecting hitherto unrecognized oestrogen receptor alpha (ERalpha)-immunoreactive neurones, we have now employed immunoprecipitation and double-label immunohistochemistry to investigate whether the ERalpha protein is present in gonadotrophin-releasing hormone (GnRH)-containing cells. The immortalized GnRH cell line GT1-7 and GnRH neurones within the rat preoptic area were found to possess ERalpha-immunoreactivity (ERalpha-IR). These observations indicate that oestrogen may regulate the synthesis and release of GnRH by direct actions on GnRH neurones.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Acrolein
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Animals
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Antibody Specificity
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Artifacts
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Cell Extracts
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Cell Line
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Cell Nucleus / chemistry
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Estrogen Receptor alpha
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Female
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Formaldehyde
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Glutaral
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Gonadotropin-Releasing Hormone / metabolism*
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Immunohistochemistry
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Molecular Weight
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Neurons / chemistry*
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Neurons / cytology
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Neurons / metabolism
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Ovariectomy
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Polymers
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Precipitin Tests
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Preoptic Area / cytology*
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Rats
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Receptors, Estrogen / analysis*
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Receptors, Estrogen / immunology
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Reproducibility of Results
Substances
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Cell Extracts
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Estrogen Receptor alpha
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Polymers
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Receptors, Estrogen
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Formaldehyde
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Gonadotropin-Releasing Hormone
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Acrolein
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Glutaral
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paraform