Distribution of estrogen receptor beta (ERβ) mRNA in hypothalamus, midbrain and temporal lobe of spayed macaque: Continued expression with hormone replacement

Chrisana Gundlah, Steven G. Kohama, Stephanie J. Mirkes, Vasilios T. Garyfallou, Henryk F. Urbanski, Cynthia L. Bethea

Research output: Contribution to journalArticlepeer-review

184 Scopus citations

Abstract

This study used in situ hybridization (ISH) to examine the distribution of estrogen receptor beta (ERβ) mRNA in hypothalamic, limbic, and midbrain regions of monkey brain and its regulation by estrogen (E) and progesterone (P). Monkey-specific ERβ cDNAs were developed with human primers and reverse transcription and polymerase chain reaction (RT-PCR) using mRNA extracted from a rhesus monkey prostate gland. ERβ 5' (262 bases) and 3' (205 bases) riboprobes were used in combination for ISH. Ovariectomized and hysterectomized (spayed) pigtail macaques (Macaca nemestrina; four per treatment group) were either untreated spayed-controls, treated with E (28 days), or treated with E plus P (14 days E+14 days E and P). Dense ERβ hybridization signal was seen in the preoptic area, paraventricular nucleus, and ventromedial nucleus of the hypothalamus; the substantia nigra, caudal linear, dorsal raphe, and pontine nuclei of the midbrain; the dentate gyrus, CA1, CA2, CA3, CA4, and the prosubiculum/subiculum areas of the hippocampus. Expression in the suprachiasmatic region, supraoptic nucleus, arcuate nucleus, and amygdala was less intense. Image analysis of the dense areas showed no significant difference in the hybridization signal in individual regions of the hypothalamus, midbrain, or hippocampus between any of the treatment groups. However, P treatment decreased overall ERβ signal in the hypothalamus and hippocampus when several different subregions were combined. The localization of ERβ in monkey brain by ISH is in general agreement with that previously described in rodents. The presence of monkey ERβ mRNA in brain regions that lack ERα should help to clarify the molecular mechanisms by which E acts in the central nervous system to influence hormone secretion, mood disorders, cognition, and neuroprotection. Copyright (C) 2000 Elsevier Science B.V.

Original languageEnglish (US)
Pages (from-to)191-204
Number of pages14
JournalMolecular Brain Research
Volume76
Issue number2
DOIs
StatePublished - Mar 29 2000

Keywords

  • Brain
  • Estrogen receptor beta
  • Hormone replacement therapy
  • Macaque
  • Ovarian steroid

ASJC Scopus subject areas

  • Molecular Biology
  • Cellular and Molecular Neuroscience

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