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Subcutaneous Adipose Tissue from Obese and Lean Adults Does Not Release Hepcidin In Vivo

Hepcidin is the main regulator of systemic iron homeostasis and is primarily produced by the liver but is also expressed, at the mRNA-level, in periphery tissues including the subcutaneous and visceral adipose tissue. Obesity is associated with elevated hepcidin concentrations and iron depletion sug...

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Autores principales: Tussing-Humphreys, Lisa, Frayn, Keith N., Smith, Steven R., Westerman, Mark, Dennis, A. Louise, Nemeth, Elizabeta, Thomson, Jessica, Pusatcioglu, Cenk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: TheScientificWorldJOURNAL 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3217603/
https://www.ncbi.nlm.nih.gov/pubmed/22125467
http://dx.doi.org/10.1100/2011/634861
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author Tussing-Humphreys, Lisa
Frayn, Keith N.
Smith, Steven R.
Westerman, Mark
Dennis, A. Louise
Nemeth, Elizabeta
Thomson, Jessica
Pusatcioglu, Cenk
author_facet Tussing-Humphreys, Lisa
Frayn, Keith N.
Smith, Steven R.
Westerman, Mark
Dennis, A. Louise
Nemeth, Elizabeta
Thomson, Jessica
Pusatcioglu, Cenk
author_sort Tussing-Humphreys, Lisa
collection PubMed
description Hepcidin is the main regulator of systemic iron homeostasis and is primarily produced by the liver but is also expressed, at the mRNA-level, in periphery tissues including the subcutaneous and visceral adipose tissue. Obesity is associated with elevated hepcidin concentrations and iron depletion suggesting that the exaggerated fat mass in obesity could contribute significantly to circulating hepcidin levels consequently altering iron homeostasis. The objective of this study was to determine if abdominal subcutaneous adipose tissue (AbScAT) releases hepcidin in vivo and if release is modified by obesity. Arterio-venous differences in concentrations of hepcidin were measured across AbScAT in 9 obese and 9 lean adults. Overall (n = 18), mean plasma hepcidin concentrations were significantly higher in arterialized compared to AbScAT venous samples [mean difference (arterialized-AbScAT venous plasma hepcidin) = 4.9 ± 9.6 ng/mL, P = 0.04]. Net regional release was not calculated because mean venous plasma hepcidin concentrations were lower than mean arterialized concentrations indicating no net release. Significant correlations between AbScAT venous and arterialized plasma hepcidin concentrations with anthropometric variables were not observed. Findings from this vein drainage study suggest there is no net release of hepcidin from the AbScAT depot and thereby no ability to signal systemically, even in obesity.
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spelling pubmed-32176032011-11-28 Subcutaneous Adipose Tissue from Obese and Lean Adults Does Not Release Hepcidin In Vivo Tussing-Humphreys, Lisa Frayn, Keith N. Smith, Steven R. Westerman, Mark Dennis, A. Louise Nemeth, Elizabeta Thomson, Jessica Pusatcioglu, Cenk ScientificWorldJournal Research Article Hepcidin is the main regulator of systemic iron homeostasis and is primarily produced by the liver but is also expressed, at the mRNA-level, in periphery tissues including the subcutaneous and visceral adipose tissue. Obesity is associated with elevated hepcidin concentrations and iron depletion suggesting that the exaggerated fat mass in obesity could contribute significantly to circulating hepcidin levels consequently altering iron homeostasis. The objective of this study was to determine if abdominal subcutaneous adipose tissue (AbScAT) releases hepcidin in vivo and if release is modified by obesity. Arterio-venous differences in concentrations of hepcidin were measured across AbScAT in 9 obese and 9 lean adults. Overall (n = 18), mean plasma hepcidin concentrations were significantly higher in arterialized compared to AbScAT venous samples [mean difference (arterialized-AbScAT venous plasma hepcidin) = 4.9 ± 9.6 ng/mL, P = 0.04]. Net regional release was not calculated because mean venous plasma hepcidin concentrations were lower than mean arterialized concentrations indicating no net release. Significant correlations between AbScAT venous and arterialized plasma hepcidin concentrations with anthropometric variables were not observed. Findings from this vein drainage study suggest there is no net release of hepcidin from the AbScAT depot and thereby no ability to signal systemically, even in obesity. TheScientificWorldJOURNAL 2011-11-09 /pmc/articles/PMC3217603/ /pubmed/22125467 http://dx.doi.org/10.1100/2011/634861 Text en Copyright © 2011 Lisa Tussing-Humphreys et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Tussing-Humphreys, Lisa
Frayn, Keith N.
Smith, Steven R.
Westerman, Mark
Dennis, A. Louise
Nemeth, Elizabeta
Thomson, Jessica
Pusatcioglu, Cenk
Subcutaneous Adipose Tissue from Obese and Lean Adults Does Not Release Hepcidin In Vivo
title Subcutaneous Adipose Tissue from Obese and Lean Adults Does Not Release Hepcidin In Vivo
title_full Subcutaneous Adipose Tissue from Obese and Lean Adults Does Not Release Hepcidin In Vivo
title_fullStr Subcutaneous Adipose Tissue from Obese and Lean Adults Does Not Release Hepcidin In Vivo
title_full_unstemmed Subcutaneous Adipose Tissue from Obese and Lean Adults Does Not Release Hepcidin In Vivo
title_short Subcutaneous Adipose Tissue from Obese and Lean Adults Does Not Release Hepcidin In Vivo
title_sort subcutaneous adipose tissue from obese and lean adults does not release hepcidin in vivo
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3217603/
https://www.ncbi.nlm.nih.gov/pubmed/22125467
http://dx.doi.org/10.1100/2011/634861
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