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Brain Aromatase and the Regulation of Sexual Activity in Male Mice

The biologically active estrogen estradiol has important roles in adult brain physiology and sexual behavior. A single gene, Cyp19a1, encodes aromatase, the enzyme that catalyzes the conversion of testosterone to estradiol in the testis and brain of male mice. Estradiol formation was shown to regula...

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Autores principales: Brooks, David C, Coon V, John S, Ercan, Cihangir M, Xu, Xia, Dong, Hongxin, Levine, Jon E, Bulun, Serdar E, Zhao, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7485274/
https://www.ncbi.nlm.nih.gov/pubmed/32910181
http://dx.doi.org/10.1210/endocr/bqaa137
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author Brooks, David C
Coon V, John S
Ercan, Cihangir M
Xu, Xia
Dong, Hongxin
Levine, Jon E
Bulun, Serdar E
Zhao, Hong
author_facet Brooks, David C
Coon V, John S
Ercan, Cihangir M
Xu, Xia
Dong, Hongxin
Levine, Jon E
Bulun, Serdar E
Zhao, Hong
author_sort Brooks, David C
collection PubMed
description The biologically active estrogen estradiol has important roles in adult brain physiology and sexual behavior. A single gene, Cyp19a1, encodes aromatase, the enzyme that catalyzes the conversion of testosterone to estradiol in the testis and brain of male mice. Estradiol formation was shown to regulate sexual activity in various species, but the relative contributions to sexual behavior of estrogen that arises in the brain versus from the gonads remained unclear. To determine the role of brain aromatase in regulating male sexual activity, we generated a brain-specific aromatase knockout (bArKO) mouse. A newly generated whole-body total aromatase knockout mouse of the same genetic background served as a positive control. Here we demonstrate that local aromatase expression and estrogen production in the brain is partially required for male sexual behavior and sex hormone homeostasis. Male bArKO mice exhibited decreased sexual activity in the presence of strikingly elevated circulating testosterone. In castrated adult bArKO mice, administration of testosterone only partially restored sexual behavior; full sexual behavior, however, was achieved only when both estradiol and testosterone were administered together. Thus, aromatase in the brain is, in part, necessary for testosterone-dependent male sexual activity. We also found that brain aromatase is required for negative feedback regulation of circulating testosterone of testicular origin. Our findings suggest testosterone activates male sexual behavior in part via conversion to estradiol in the brain. These studies provide foundational evidence that sexual behavior may be modified through inhibition or enhancement of brain aromatase enzyme activity and/or utilization of selective estrogen receptor modulators.
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spelling pubmed-74852742020-09-15 Brain Aromatase and the Regulation of Sexual Activity in Male Mice Brooks, David C Coon V, John S Ercan, Cihangir M Xu, Xia Dong, Hongxin Levine, Jon E Bulun, Serdar E Zhao, Hong Endocrinology Research Articles The biologically active estrogen estradiol has important roles in adult brain physiology and sexual behavior. A single gene, Cyp19a1, encodes aromatase, the enzyme that catalyzes the conversion of testosterone to estradiol in the testis and brain of male mice. Estradiol formation was shown to regulate sexual activity in various species, but the relative contributions to sexual behavior of estrogen that arises in the brain versus from the gonads remained unclear. To determine the role of brain aromatase in regulating male sexual activity, we generated a brain-specific aromatase knockout (bArKO) mouse. A newly generated whole-body total aromatase knockout mouse of the same genetic background served as a positive control. Here we demonstrate that local aromatase expression and estrogen production in the brain is partially required for male sexual behavior and sex hormone homeostasis. Male bArKO mice exhibited decreased sexual activity in the presence of strikingly elevated circulating testosterone. In castrated adult bArKO mice, administration of testosterone only partially restored sexual behavior; full sexual behavior, however, was achieved only when both estradiol and testosterone were administered together. Thus, aromatase in the brain is, in part, necessary for testosterone-dependent male sexual activity. We also found that brain aromatase is required for negative feedback regulation of circulating testosterone of testicular origin. Our findings suggest testosterone activates male sexual behavior in part via conversion to estradiol in the brain. These studies provide foundational evidence that sexual behavior may be modified through inhibition or enhancement of brain aromatase enzyme activity and/or utilization of selective estrogen receptor modulators. Oxford University Press 2020-09-10 /pmc/articles/PMC7485274/ /pubmed/32910181 http://dx.doi.org/10.1210/endocr/bqaa137 Text en Published by Oxford University Press on behalf of the Endocrine Society 2020. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Brooks, David C
Coon V, John S
Ercan, Cihangir M
Xu, Xia
Dong, Hongxin
Levine, Jon E
Bulun, Serdar E
Zhao, Hong
Brain Aromatase and the Regulation of Sexual Activity in Male Mice
title Brain Aromatase and the Regulation of Sexual Activity in Male Mice
title_full Brain Aromatase and the Regulation of Sexual Activity in Male Mice
title_fullStr Brain Aromatase and the Regulation of Sexual Activity in Male Mice
title_full_unstemmed Brain Aromatase and the Regulation of Sexual Activity in Male Mice
title_short Brain Aromatase and the Regulation of Sexual Activity in Male Mice
title_sort brain aromatase and the regulation of sexual activity in male mice
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7485274/
https://www.ncbi.nlm.nih.gov/pubmed/32910181
http://dx.doi.org/10.1210/endocr/bqaa137
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