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Aromatase Blockade Is Associated With Increased Mortality in Acute Illness in Male Mice
CONTEXT: The increase in circulating estrogen levels with acute illness in humans is accompanied by increased aromatase expression in adipose tissue and increased peripheral aromatization of estrogens to androgens. Animal studies indicate that estrogen may be beneficial in acute illness. OBJECTIVE:...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Endocrine Society
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686622/ https://www.ncbi.nlm.nih.gov/pubmed/29264565 http://dx.doi.org/10.1210/js.2017-00128 |
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author | Connerney, Jeannette J. Spratt, Daniel I. |
author_facet | Connerney, Jeannette J. Spratt, Daniel I. |
author_sort | Connerney, Jeannette J. |
collection | PubMed |
description | CONTEXT: The increase in circulating estrogen levels with acute illness in humans is accompanied by increased aromatase expression in adipose tissue and increased peripheral aromatization of estrogens to androgens. Animal studies indicate that estrogen may be beneficial in acute illness. OBJECTIVE: We hypothesized that blockade of aromatase in acute illness would decrease survival. DESIGN: Prospective sham controlled. SETTING: Maine Medical Center Research Institute animal facility. ANIMALS: Six- to 8-week-old male black 6 mice. INTERVENTION: Mice underwent cecal ligation and puncture (CLP) to induce acute illness and were administered letrozole to block aromatase or saline. Mice undergoing sham surgery with or without letrozole served as controls. Adipose and cardiovascular tissue was harvested for preliminary evaluation of aromatase expression. MAIN OUTCOME MEASUREMENTS: Survival was the main outcome measurement. Evidence for aromatase expression in tissue samples was assessed using western blot and/or immunohistochemistry. RESULTS: With aromatase blockade, survival in CLP mice was decreased (P = 0.04). The presence of aromatase in adipose tissue was observed by western blot in CLP but not control mice. Similarly, the presence of aromatase was observed in cardiac tissue of CLP but not in control mice. CONCLUSIONS: The decreased survival during sepsis with aromatase blockade suggests that this response to acute illness may be important both physiologically and clinically. The preliminary observation of aromatase expression in adipose and cardiovascular tissue during acute illness in this mouse model indicates that this model has parallels to human physiology and may be useful for further studying the aromatase response to acute illness. |
format | Online Article Text |
id | pubmed-5686622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Endocrine Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-56866222017-12-20 Aromatase Blockade Is Associated With Increased Mortality in Acute Illness in Male Mice Connerney, Jeannette J. Spratt, Daniel I. J Endocr Soc Clinical Research Article CONTEXT: The increase in circulating estrogen levels with acute illness in humans is accompanied by increased aromatase expression in adipose tissue and increased peripheral aromatization of estrogens to androgens. Animal studies indicate that estrogen may be beneficial in acute illness. OBJECTIVE: We hypothesized that blockade of aromatase in acute illness would decrease survival. DESIGN: Prospective sham controlled. SETTING: Maine Medical Center Research Institute animal facility. ANIMALS: Six- to 8-week-old male black 6 mice. INTERVENTION: Mice underwent cecal ligation and puncture (CLP) to induce acute illness and were administered letrozole to block aromatase or saline. Mice undergoing sham surgery with or without letrozole served as controls. Adipose and cardiovascular tissue was harvested for preliminary evaluation of aromatase expression. MAIN OUTCOME MEASUREMENTS: Survival was the main outcome measurement. Evidence for aromatase expression in tissue samples was assessed using western blot and/or immunohistochemistry. RESULTS: With aromatase blockade, survival in CLP mice was decreased (P = 0.04). The presence of aromatase in adipose tissue was observed by western blot in CLP but not control mice. Similarly, the presence of aromatase was observed in cardiac tissue of CLP but not in control mice. CONCLUSIONS: The decreased survival during sepsis with aromatase blockade suggests that this response to acute illness may be important both physiologically and clinically. The preliminary observation of aromatase expression in adipose and cardiovascular tissue during acute illness in this mouse model indicates that this model has parallels to human physiology and may be useful for further studying the aromatase response to acute illness. Endocrine Society 2017-07-14 /pmc/articles/PMC5686622/ /pubmed/29264565 http://dx.doi.org/10.1210/js.2017-00128 Text en Copyright © 2017 Endocrine Society https://creativecommons.org/licenses/by-nc-nd/4.0/ This article has been published under the terms of the Creative Commons Attribution Non-Commercial, No-Derivatives License (CC BY-NC-ND; https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Clinical Research Article Connerney, Jeannette J. Spratt, Daniel I. Aromatase Blockade Is Associated With Increased Mortality in Acute Illness in Male Mice |
title | Aromatase Blockade Is Associated With Increased Mortality in Acute Illness in Male Mice |
title_full | Aromatase Blockade Is Associated With Increased Mortality in Acute Illness in Male Mice |
title_fullStr | Aromatase Blockade Is Associated With Increased Mortality in Acute Illness in Male Mice |
title_full_unstemmed | Aromatase Blockade Is Associated With Increased Mortality in Acute Illness in Male Mice |
title_short | Aromatase Blockade Is Associated With Increased Mortality in Acute Illness in Male Mice |
title_sort | aromatase blockade is associated with increased mortality in acute illness in male mice |
topic | Clinical Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686622/ https://www.ncbi.nlm.nih.gov/pubmed/29264565 http://dx.doi.org/10.1210/js.2017-00128 |
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