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Nutrition Department, The Pennsylvania State University, University Park, PA 16802
3To whom correspondence should be addressed.
In view of evidence that nutritional status of iron and vitamin A may affect the other nutrients metabolism, we used model-based compartmental analysis to examine effects of iron deficiency on whole-body vitamin A dynamics in rats. Weanling male Sprague-Dawley rats were fed the AIN93G diet with 2.5 nmol retinyl palmitate/g and either 45 [control (CN)] or 4 µg/g Fe [iron-deficient (ID)] for 8 wk. ID rats consumed food ad libitum; CN rats were food-restricted so that their body weights were the same as ID rats. Two rats/group were killed; liver vitamin A was determined and used for vitamin A balance calculations. [3H]Retinol-labeled plasma was administered intravenously to remaining rats, and 27 serial blood samples were collected for 7 wk. At killing, plasma vitamin A was 0.52 ± 0.12 (ID, n = 5) vs. 1.34 ± 0.12 µmol/L (CN, n = 6; P < 0.001), and liver vitamin A was 809 ± 94 (ID) vs. 112 ± 24 nmol (CN, P < 0.001). Plasma tracer data were fit to a three- or four-compartment model using the Simulation, Analysis and Modeling computer program and kinetic parameters were calculated. Vitamin A transfer rate between the retinyl ester storage pool [14 ± 3 (ID) vs. 24 ± 4 nmol/d (CN), P < 0.05] and plasma was lower in ID rats. Vitamin A remained longer in the body [44 ± 11 (ID) vs. 22 ± 3 d (CN), P < 0.05]. Adjusted mean disposal rate was lower in ID (10.0) than CN rats (19.9 nmol/d), as was estimated vitamin A absorption efficiency [58% (ID) vs. 76% (CN)]. Our results suggest that iron deficiency inhibits mobilization of vitamin A stores and may decrease the absorption and irreversible utilization of vitamin A.
KEY WORDS: iron deficiency vitamin A kinetics simulation, analysis and modeling rats
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