RGD Reference Report - Iron supplementation moderates but does not cure the Belgrade anemia. - Rat Genome Database

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Iron supplementation moderates but does not cure the Belgrade anemia.

Authors: Garrick, M  Scott, D  Walpole, S  Finkelstein, E  Whitbred, J  Chopra, S  Trivikram, L  Mayes, D  Rhodes, D  Cabbagestalk, K  Oklu, R  Sadiq, A  Mascia, B  Hoke, J  Garrick, L 
Citation: Garrick M, etal., Biometals. 1997 Apr;10(2):65-76.
RGD ID: 1578513
Pubmed: PMID:9210290   (View Abstract at PubMed)

Belgrade rats inherit microcytic, hypochromic anemia as an autosomal recessive trait (gene symbol b). Erythrocytes and tissue are iron deficient in the face of elevated TIBC (total iron binding capacity) and percent iron saturation; iron injections increased the number of erythrocytes but their appearance remained abnormal. We have investigated iron supplements to improve husbandry of b/b rats and to learn more about the underlying defect and its tissue distribution. Weekly i.m. (intramuscular) injections of iron-dextran (Imferon at 30 mg kg-1) improved the anemia but did not alter the red cell morphology. Certain diets also improved the health of b/b rats when compared to standard rat chows by the criteria of weight, survival to adulthood, hematology and reproduction. The critical nutritional factor turned out to be iron bioavailability, with ferrous iron added to the diet improving the health of Belgrade rats without affecting the underlying erythroid defect. Tissue iron measurements after dietary or parenteral supplementation confirmed the iron deficient status of untreated b/b rats and established that dietary ferrous iron partially relieved this deficiency, with injections leading to greater amounts of tissue iron. Serum iron and TIBC were also found to be elevated in untreated b/b rats, with dietary supplementation decreasing but not eliminating the elevation in TIBC. These studies indicate that iron supplements can improve the health of b/b rats without altering the underlying defect and also suggest that the mutation could alter iron uptake in the GI (gastrointestinal) tract.

Phenotype Annotations    

Mammalian Phenotype
Objects Annotated

BG  (anemic Belgrade)

Additional Information