Journal
ENDOCRINOLOGY
Volume 147, Issue 1, Pages 415-420Publisher
ENDOCRINE SOC
DOI: 10.1210/en.2005-0834
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Funding
- NIMH NIH HHS [R01 MH57759, K02 MH01349, F31 MH70092] Funding Source: Medline
- NATIONAL INSTITUTE OF MENTAL HEALTH [F31MH070092, R01MH057759, K02MH001349] Funding Source: NIH RePORTER
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Sexual dimorphisms in the hypothalamus are mediated in several cases by local aromatization of androgens to estrogens during the perinatal period. In this series of experiments, the contributions of the two estrogen receptors (ERs), ER alpha and ER beta, to the differentiation of the sexually dimorphic subpopulation of dopaminergic neurons in the anteroventral periventricular area (AVPV) was examined. In the first experiment, numbers of tyrosine hydroxylase (TH) immunoreactive (-ir) AVPV neurons in ER beta knockout and wild- type (WT) mice of both sexes were measured. In the second experiment, the average number of TH-ir neurons in the medial portion of the AVPV in ER alpha knockout, ER beta knockout, double-ER knockout, and WT mice of both sexes was calculated. In both experiments TH-ir cell numbers were sexually dimorphic as expected, more TH-ir neurons than WT males. Interestingly the average number of TH-ir neurons in all knockout males was significantly higher than in WT male littermates. In fact, TH-ir cell numbers in all knockout males were equivalent to females. In a final experiment, C57BL/6J female mice were treated during the first 3 postnatal days with either estradiol, or a specific agonist for one of the two ERs. Additional male and female pups received vehicle injections. Treatments with estradiol or either ER-specific agonist significantly reduced the number of TH-ir AVPV neurons in female brains. Our data demonstrate that both ER alpha and ER beta are involved in the sexual differentiation of the AVPV in mice.
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