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Endogenous Glucocorticoid Metabolism in Bone: Friend or Foe

The role of tissue specific metabolism of endogenous glucocorticoids (GCs) in the pathogenesis of human disease has been a field of intense interest over the last 20 years, fuelling clinical trials of metabolism inhibitors in the treatment of an array of metabolic diseases. Localised pre-receptor me...

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Autores principales: Martin, Claire S., Cooper, Mark S., Hardy, Rowan S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8429897/
https://www.ncbi.nlm.nih.gov/pubmed/34512556
http://dx.doi.org/10.3389/fendo.2021.733611
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author Martin, Claire S.
Cooper, Mark S.
Hardy, Rowan S.
author_facet Martin, Claire S.
Cooper, Mark S.
Hardy, Rowan S.
author_sort Martin, Claire S.
collection PubMed
description The role of tissue specific metabolism of endogenous glucocorticoids (GCs) in the pathogenesis of human disease has been a field of intense interest over the last 20 years, fuelling clinical trials of metabolism inhibitors in the treatment of an array of metabolic diseases. Localised pre-receptor metabolism of endogenous and therapeutic GCs by the 11β-hydroxysteroid dehydrogenase (11β-HSD) enzymes (which interconvert endogenous GCs between their inactive and active forms) are increasingly recognised as being critical in mediating both their positive and negative actions on bone homeostasis. In this review we explore the roles of endogenous and therapeutic GC metabolism by the 11β-HSD enzymes in the context of bone metabolism and bone cell function, and consider future strategies aimed at modulating this system in order to manage and treat various bone diseases.
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spelling pubmed-84298972021-09-11 Endogenous Glucocorticoid Metabolism in Bone: Friend or Foe Martin, Claire S. Cooper, Mark S. Hardy, Rowan S. Front Endocrinol (Lausanne) Endocrinology The role of tissue specific metabolism of endogenous glucocorticoids (GCs) in the pathogenesis of human disease has been a field of intense interest over the last 20 years, fuelling clinical trials of metabolism inhibitors in the treatment of an array of metabolic diseases. Localised pre-receptor metabolism of endogenous and therapeutic GCs by the 11β-hydroxysteroid dehydrogenase (11β-HSD) enzymes (which interconvert endogenous GCs between their inactive and active forms) are increasingly recognised as being critical in mediating both their positive and negative actions on bone homeostasis. In this review we explore the roles of endogenous and therapeutic GC metabolism by the 11β-HSD enzymes in the context of bone metabolism and bone cell function, and consider future strategies aimed at modulating this system in order to manage and treat various bone diseases. Frontiers Media S.A. 2021-08-27 /pmc/articles/PMC8429897/ /pubmed/34512556 http://dx.doi.org/10.3389/fendo.2021.733611 Text en Copyright © 2021 Martin, Cooper and Hardy https://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
Martin, Claire S.
Cooper, Mark S.
Hardy, Rowan S.
Endogenous Glucocorticoid Metabolism in Bone: Friend or Foe
title Endogenous Glucocorticoid Metabolism in Bone: Friend or Foe
title_full Endogenous Glucocorticoid Metabolism in Bone: Friend or Foe
title_fullStr Endogenous Glucocorticoid Metabolism in Bone: Friend or Foe
title_full_unstemmed Endogenous Glucocorticoid Metabolism in Bone: Friend or Foe
title_short Endogenous Glucocorticoid Metabolism in Bone: Friend or Foe
title_sort endogenous glucocorticoid metabolism in bone: friend or foe
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8429897/
https://www.ncbi.nlm.nih.gov/pubmed/34512556
http://dx.doi.org/10.3389/fendo.2021.733611
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