Storage iron exchange in the rat as affected by deferoxamine
Journal Article
·
· J. Lab. Clin. Med.; (United States)
OSTI ID:5569484
The initial tissue localization and redistribution of radioactive iron injected intravenously into the rat as ferritin, chondroitin sulfate, and nonviable red cells was determined. Ferritin iron, initially localized in the hepatocyte, showed minimal redistribution over 24 hours in the normal animal. This may be compared with the active release of iron from the reticuloendothelial cell after the intravenous injection of nonviable red cells and chondroitin sulfate iron. All forms of iron were actively mobilized in iron-deficient animals. The effect of chelation of iron by deferoxamine (DFO) on the redistribution pattern over 4 to 6 hours was determined in iron-deficient, normal, iron-loaded, and phenylhydrazine-treated rats to evaluate the effect of iron stores and erythropoiesis. Use of DFO resulted in extensive chelation of radioactive iron within the hepatocyte and greatly reduced the amount of hepatocyte iron available for erythropoiesis. Very little chelation of reticuloendothelial cell-processed iron occurred, and there was little decrease in its utilization for red cell production. Total urinary chelate iron was independent of erythropoiesis but varied in parallel with the iron load of the animal. These studies suggest that DFO does not act on the reticuloendothelial cell but does have at least two sites of action, both of which relate to total storage iron. One involves hepatocyte stores with excretion into the intestinal tract. The other, possibly located at the hepatocyte membrane, results in urinary iron excretion.
- Research Organization:
- Seoul National Univ., Korea
- OSTI ID:
- 5569484
- Journal Information:
- J. Lab. Clin. Med.; (United States), Journal Name: J. Lab. Clin. Med.; (United States) Vol. 105:4; ISSN JLCMA
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
550201* -- Biochemistry-- Tracer Techniques
59 BASIC BIOLOGICAL SCIENCES
AMINES
ANEMIAS
ANIMAL CELLS
ANIMAL TISSUES
ANIMALS
BIOCHEMICAL REACTION KINETICS
BIOLOGICAL EFFECTS
BIOLOGICAL LOCALIZATION
BIOLOGICAL MATERIALS
BIOLOGICAL PATHWAYS
BLOOD
BLOOD CELLS
BLOOD FORMATION
BODY
BODY FLUIDS
CHELATING AGENTS
COMPLEXES
DEFEROXAMINE
DISEASES
DISTRIBUTION
ELEMENTS
ERYTHROCYTES
FERRITIN
HEMIC DISEASES
INJECTION
INTAKE
INTRAVENOUS INJECTION
IRON
IRON COMPLEXES
IRON ISOTOPES
ISOTOPE APPLICATIONS
ISOTOPES
KINETICS
LIVER CELLS
MAMMALS
MATERIALS
METALLOPROTEINS
METALS
ORGANIC COMPOUNDS
PROTEINS
RATS
REACTION KINETICS
RETICULOENDOTHELIAL SYSTEM
RODENTS
SOMATIC CELLS
SYMPTOMS
TISSUE DISTRIBUTION
TISSUES
TRACER TECHNIQUES
TRANSITION ELEMENT COMPLEXES
TRANSITION ELEMENTS
VERTEBRATES
WEIGHT
59 BASIC BIOLOGICAL SCIENCES
AMINES
ANEMIAS
ANIMAL CELLS
ANIMAL TISSUES
ANIMALS
BIOCHEMICAL REACTION KINETICS
BIOLOGICAL EFFECTS
BIOLOGICAL LOCALIZATION
BIOLOGICAL MATERIALS
BIOLOGICAL PATHWAYS
BLOOD
BLOOD CELLS
BLOOD FORMATION
BODY
BODY FLUIDS
CHELATING AGENTS
COMPLEXES
DEFEROXAMINE
DISEASES
DISTRIBUTION
ELEMENTS
ERYTHROCYTES
FERRITIN
HEMIC DISEASES
INJECTION
INTAKE
INTRAVENOUS INJECTION
IRON
IRON COMPLEXES
IRON ISOTOPES
ISOTOPE APPLICATIONS
ISOTOPES
KINETICS
LIVER CELLS
MAMMALS
MATERIALS
METALLOPROTEINS
METALS
ORGANIC COMPOUNDS
PROTEINS
RATS
REACTION KINETICS
RETICULOENDOTHELIAL SYSTEM
RODENTS
SOMATIC CELLS
SYMPTOMS
TISSUE DISTRIBUTION
TISSUES
TRACER TECHNIQUES
TRANSITION ELEMENT COMPLEXES
TRANSITION ELEMENTS
VERTEBRATES
WEIGHT