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Pathophysiology of the Belgrade rat

The Belgrade rat is an animal model of divalent metal transporter 1 (DMT1) deficiency. This strain originates from an X-irradiation experiment first reported in 1966. Since then, the Belgrade rat’s pathophysiology has helped to reveal the importance of iron balance and the role of DMT1. This review...

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Autores principales: Veuthey, Tania, Wessling-Resnick, Marianne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4000996/
https://www.ncbi.nlm.nih.gov/pubmed/24795636
http://dx.doi.org/10.3389/fphar.2014.00082
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author Veuthey, Tania
Wessling-Resnick, Marianne
author_facet Veuthey, Tania
Wessling-Resnick, Marianne
author_sort Veuthey, Tania
collection PubMed
description The Belgrade rat is an animal model of divalent metal transporter 1 (DMT1) deficiency. This strain originates from an X-irradiation experiment first reported in 1966. Since then, the Belgrade rat’s pathophysiology has helped to reveal the importance of iron balance and the role of DMT1. This review discusses our current understanding of iron transport homeostasis and summarizes molecular details of DMT1 function. We describe how studies of the Belgrade rat have revealed key roles for DMT1 in iron distribution to red blood cells as well as duodenal iron absorption. The Belgrade rat’s pathology has extended our knowledge of hepatic iron handling, pulmonary and olfactory iron transport as well as brain iron uptake and renal iron handling. For example, relationships between iron and manganese metabolism have been discerned since both are essential metals transported by DMT1. Pathophysiologic features of the Belgrade rat provide us with a unique and interesting animal model to understand iron homeostasis.
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spelling pubmed-40009962014-05-02 Pathophysiology of the Belgrade rat Veuthey, Tania Wessling-Resnick, Marianne Front Pharmacol Pharmacology The Belgrade rat is an animal model of divalent metal transporter 1 (DMT1) deficiency. This strain originates from an X-irradiation experiment first reported in 1966. Since then, the Belgrade rat’s pathophysiology has helped to reveal the importance of iron balance and the role of DMT1. This review discusses our current understanding of iron transport homeostasis and summarizes molecular details of DMT1 function. We describe how studies of the Belgrade rat have revealed key roles for DMT1 in iron distribution to red blood cells as well as duodenal iron absorption. The Belgrade rat’s pathology has extended our knowledge of hepatic iron handling, pulmonary and olfactory iron transport as well as brain iron uptake and renal iron handling. For example, relationships between iron and manganese metabolism have been discerned since both are essential metals transported by DMT1. Pathophysiologic features of the Belgrade rat provide us with a unique and interesting animal model to understand iron homeostasis. Frontiers Media S.A. 2014-04-22 /pmc/articles/PMC4000996/ /pubmed/24795636 http://dx.doi.org/10.3389/fphar.2014.00082 Text en Copyright © 2014 Veuthey and Wessling-Resnick. http://creativecommons.org/licenses/by/3.0/ 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) or licensor 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 Pharmacology
Veuthey, Tania
Wessling-Resnick, Marianne
Pathophysiology of the Belgrade rat
title Pathophysiology of the Belgrade rat
title_full Pathophysiology of the Belgrade rat
title_fullStr Pathophysiology of the Belgrade rat
title_full_unstemmed Pathophysiology of the Belgrade rat
title_short Pathophysiology of the Belgrade rat
title_sort pathophysiology of the belgrade rat
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4000996/
https://www.ncbi.nlm.nih.gov/pubmed/24795636
http://dx.doi.org/10.3389/fphar.2014.00082
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