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Cognitive Effects of Aromatase and Possible Role in Memory Disorders

Diverse cognitive functions in many vertebrate species are influenced by local conversion of androgens to 17β-estradiol (E2) by aromatase. This enzyme is highly expressed in various brain regions across species, with some inter-species variation in terms of regional brain expression. Since women wit...

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Autores principales: Rosenfeld, Cheryl S., Shay, Dusti A., Vieira-Potter, Victoria J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6199361/
https://www.ncbi.nlm.nih.gov/pubmed/30386297
http://dx.doi.org/10.3389/fendo.2018.00610
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author Rosenfeld, Cheryl S.
Shay, Dusti A.
Vieira-Potter, Victoria J.
author_facet Rosenfeld, Cheryl S.
Shay, Dusti A.
Vieira-Potter, Victoria J.
author_sort Rosenfeld, Cheryl S.
collection PubMed
description Diverse cognitive functions in many vertebrate species are influenced by local conversion of androgens to 17β-estradiol (E2) by aromatase. This enzyme is highly expressed in various brain regions across species, with some inter-species variation in terms of regional brain expression. Since women with breast cancer and men and women with other disorders are often treated with aromatase inhibitors (AI), these populations might be especially vulnerable to cognitive deficits due to low neuroE2 synthesis, i.e., synthesis of E2 directly within the brain. Animal models have been useful in deciphering aromatase effects on cognitive functions. Consequences of AI administration at various life cycle stages have been assessed on auditory, song processing, and spatial memory in birds and various aspects of cognition in rodent models. Additionally, cognitive deficits have been described in aromatase knockout (ArKO) mice that systemically lack this gene throughout their lifespan. This review will consider evidence to date that AI treatment in male and female rodent models, birds, and humans results in cognitive impairments. How brain aromatase regulates cognitive function throughout the lifespan, and gaps in current knowledge will be considered, along with future directions to better define how aromatase might guide learning and memory from early development through the geriatric period. Better understanding the importance of E2 synthesis on neurobehavioral responses at various ages will likely aid in the discovery of therapeutic strategies to prevent potential cognitive deficits, including Alzheimer's Disease, in individuals treated with AI or those possessing CYP19 gene polymorphisms, as well as cognitive effects of normal aging that may be related to changes in brain aromatase activity.
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spelling pubmed-61993612018-11-01 Cognitive Effects of Aromatase and Possible Role in Memory Disorders Rosenfeld, Cheryl S. Shay, Dusti A. Vieira-Potter, Victoria J. Front Endocrinol (Lausanne) Endocrinology Diverse cognitive functions in many vertebrate species are influenced by local conversion of androgens to 17β-estradiol (E2) by aromatase. This enzyme is highly expressed in various brain regions across species, with some inter-species variation in terms of regional brain expression. Since women with breast cancer and men and women with other disorders are often treated with aromatase inhibitors (AI), these populations might be especially vulnerable to cognitive deficits due to low neuroE2 synthesis, i.e., synthesis of E2 directly within the brain. Animal models have been useful in deciphering aromatase effects on cognitive functions. Consequences of AI administration at various life cycle stages have been assessed on auditory, song processing, and spatial memory in birds and various aspects of cognition in rodent models. Additionally, cognitive deficits have been described in aromatase knockout (ArKO) mice that systemically lack this gene throughout their lifespan. This review will consider evidence to date that AI treatment in male and female rodent models, birds, and humans results in cognitive impairments. How brain aromatase regulates cognitive function throughout the lifespan, and gaps in current knowledge will be considered, along with future directions to better define how aromatase might guide learning and memory from early development through the geriatric period. Better understanding the importance of E2 synthesis on neurobehavioral responses at various ages will likely aid in the discovery of therapeutic strategies to prevent potential cognitive deficits, including Alzheimer's Disease, in individuals treated with AI or those possessing CYP19 gene polymorphisms, as well as cognitive effects of normal aging that may be related to changes in brain aromatase activity. Frontiers Media S.A. 2018-10-17 /pmc/articles/PMC6199361/ /pubmed/30386297 http://dx.doi.org/10.3389/fendo.2018.00610 Text en Copyright © 2018 Rosenfeld, Shay and Vieira-Potter. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Rosenfeld, Cheryl S.
Shay, Dusti A.
Vieira-Potter, Victoria J.
Cognitive Effects of Aromatase and Possible Role in Memory Disorders
title Cognitive Effects of Aromatase and Possible Role in Memory Disorders
title_full Cognitive Effects of Aromatase and Possible Role in Memory Disorders
title_fullStr Cognitive Effects of Aromatase and Possible Role in Memory Disorders
title_full_unstemmed Cognitive Effects of Aromatase and Possible Role in Memory Disorders
title_short Cognitive Effects of Aromatase and Possible Role in Memory Disorders
title_sort cognitive effects of aromatase and possible role in memory disorders
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6199361/
https://www.ncbi.nlm.nih.gov/pubmed/30386297
http://dx.doi.org/10.3389/fendo.2018.00610
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