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The Glucocorticoid Receptor: A Revisited Target for Toxins
The hypothalamic-pituitary-adrenal (HPA) axis activation and glucocorticoid responses are critical for survival from a number of bacterial, viral and toxic insults, demonstrated by the fact that removal of the HPA axis or GR blockade enhances mortality rates. Replacement with synthetic glucocorticoi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3153245/ https://www.ncbi.nlm.nih.gov/pubmed/22069642 http://dx.doi.org/10.3390/toxins2061357 |
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author | Marketon, Jeanette I. Webster Sternberg, Esther M. |
author_facet | Marketon, Jeanette I. Webster Sternberg, Esther M. |
author_sort | Marketon, Jeanette I. Webster |
collection | PubMed |
description | The hypothalamic-pituitary-adrenal (HPA) axis activation and glucocorticoid responses are critical for survival from a number of bacterial, viral and toxic insults, demonstrated by the fact that removal of the HPA axis or GR blockade enhances mortality rates. Replacement with synthetic glucocorticoids reverses these effects by providing protection against lethal effects. Glucocorticoid resistance/insensitivity is a common problem in the treatment of many diseases. Much research has focused on the molecular mechanism behind this resistance, but an area that has been neglected is the role of infectious agents and toxins. We have recently shown that the anthrax lethal toxin is able to repress glucocorticoid receptor function. Data suggesting that the glucocorticoid receptor may be a target for a variety of toxins is reviewed here. These studies have important implications for glucocorticoid therapy. |
format | Online Article Text |
id | pubmed-3153245 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-31532452011-11-08 The Glucocorticoid Receptor: A Revisited Target for Toxins Marketon, Jeanette I. Webster Sternberg, Esther M. Toxins (Basel) Review The hypothalamic-pituitary-adrenal (HPA) axis activation and glucocorticoid responses are critical for survival from a number of bacterial, viral and toxic insults, demonstrated by the fact that removal of the HPA axis or GR blockade enhances mortality rates. Replacement with synthetic glucocorticoids reverses these effects by providing protection against lethal effects. Glucocorticoid resistance/insensitivity is a common problem in the treatment of many diseases. Much research has focused on the molecular mechanism behind this resistance, but an area that has been neglected is the role of infectious agents and toxins. We have recently shown that the anthrax lethal toxin is able to repress glucocorticoid receptor function. Data suggesting that the glucocorticoid receptor may be a target for a variety of toxins is reviewed here. These studies have important implications for glucocorticoid therapy. MDPI 2010-06-09 /pmc/articles/PMC3153245/ /pubmed/22069642 http://dx.doi.org/10.3390/toxins2061357 Text en © 2010 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Marketon, Jeanette I. Webster Sternberg, Esther M. The Glucocorticoid Receptor: A Revisited Target for Toxins |
title | The Glucocorticoid Receptor: A Revisited Target for Toxins |
title_full | The Glucocorticoid Receptor: A Revisited Target for Toxins |
title_fullStr | The Glucocorticoid Receptor: A Revisited Target for Toxins |
title_full_unstemmed | The Glucocorticoid Receptor: A Revisited Target for Toxins |
title_short | The Glucocorticoid Receptor: A Revisited Target for Toxins |
title_sort | glucocorticoid receptor: a revisited target for toxins |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3153245/ https://www.ncbi.nlm.nih.gov/pubmed/22069642 http://dx.doi.org/10.3390/toxins2061357 |
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