J. Anim Sci.
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J. Anim Sci. 1986. 62:804-812.
© 1986 American Society of Animal Science

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Vanadium Metabolism in Sheep. III. Influence of Dietary Vanadium on Kinetics of 48V Administered Orally or Intravenously and Comparison of Compartmental and Graphical Models1,2,

S. L. Hansard, II3, C. B. Ammerman4, P. R. Henry4 and B. W. Patterson5

University of Florida, Gainesville 32611

Abstract

Radiotracer techniques were used to investigate the influence of dietary stable V on the excretion, distribution and blood clearance kinetics of 48V in 14 rams averaging 58 kg body weight. Rams were fed a basal diet with added levels of 0, 50 or 200 mg/kg V as NH4VO3 for 25 wk before either oral or iv administration of the isotope. A three-compartment model was determined by graphical logarithmic analysis of blood disappearance data from iv-dosed rams and compared with a simultaneous multicompartment model, which made it possible to ascribe physiological processes to the components of the graphical model. The principal route of excretion of 48V administered iv was via urine, whereas the isotope given orally was excreted almost entirely by way of feces, resulting in low tissue and urinary 48V levels. Increasing dietary V increased (P<.05) the percentage of dose excreted in urine regardless of dosing route, but dietary V had no effect on 48V excreted in feces. Stable dietary V had no effect on blood clearance rates of orally or iv-dosed rams. Dietary V addition decreased 48V concentration in kidney (P<.01), liver, spleen, testes and muscle (P<.05) of iv-dosed rams, but had no effect in rams dosed orally. Kidney, bone, liver and spleen retained the highest levels of 48V activity 144 h after dosing. Dietary V appeared to have a minimal effect on V kinetics in rams.


Footnotes

1 Florida Agr. Exp. Sta. Journal Ser. No. 6263.

2 The authors acknowledge American Cyanamid Co., Princeton, NJ; Int. Minerals and Chem. Corp., Mundelein, IL; Moorman Manufacturing Co., Quincy, IL; and Occidental Chem. Co., Houston, TX for funds in support of this research; Pfizer, Inc., Terre Haute, IN for supplying vitamins A and D; Monsanto Chem. Co., St. Louis, MO for supplying ethoxyquin and L. A. Zech, Natl. Inst. of Health, Bethesda, MD for assistance with the SAAM model.

3 Present address: Food and Drug Administration (HFV-128), 5600 Fishers Lane, Rockville, MD 20857.

4 Dept. of Anim. Sci.

5 Dept. of Med., College of Med.







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Copyright © 1986 by the American Society of Animal Science.