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Pathophysiology of the Belgrade rat
Tania Veuthey1, Marianne Wessling-Resnick1
1Department of Genetics and Complex Diseases, Harvard School of Public Health Boston, MA, USA.
Frontiers in Pharmacology
|May 6, 2014
Summary
The Belgrade rat, a model for divalent metal transporter 1 (DMT1) deficiency, illuminates iron homeostasis. Studies reveal DMT1
Area of Science:
- Physiology
- Genetics
- Biochemistry
Background:
- The Belgrade rat, originating from X-irradiation in 1966, serves as a model for divalent metal transporter 1 (DMT1) deficiency.
- Pathophysiological studies of this strain have been crucial in understanding iron balance and DMT1's role.
Purpose of the Study:
- To review current knowledge of iron transport homeostasis.
- To summarize molecular details of DMT1 function.
- To highlight the Belgrade rat's contribution to understanding iron metabolism.
Main Methods:
- Review of existing literature and studies involving the Belgrade rat model.
- Analysis of pathophysiological data related to DMT1 deficiency.
- Molecular characterization of DMT1 function.
Main Results:
- Studies using the Belgrade rat have elucidated DMT1's critical roles in red blood cell iron distribution and duodenal iron absorption.
- The model has expanded understanding of iron handling in the liver, lungs, olfactory system, brain, and kidneys.
- Key relationships between iron and manganese metabolism have been identified due to their shared transport by DMT1.
Conclusions:
- The Belgrade rat is an invaluable animal model for investigating iron homeostasis.
- DMT1 plays a fundamental role in the transport of essential metals, including iron and manganese.
- Further research utilizing this model promises deeper insights into metal transport disorders.

