Cd. Seaborn et al., CHROMIUM AND CHRONIC ASCORBIC-ACID DEPLETION EFFECTS ON TISSUE ASCORBATE, MANGANESE, AND C-14 RETENTION FROM C-14 ASCORBATE IN GUINEA-PIGS, Biological trace element research, 41(3), 1994, pp. 279-294
Chromium (Cr) potentiates the effects of insulin and a role for insuli
n in ascorbic acid transport has been reported. Therefore, the effects
of Cr and ascorbate depletion on tissue ascorbic acid and C-14 distri
bution and excretion after a C-14 ascorbate dose were investigated in
guinea pigs. As utilization of dietary Cr is affected by interaction w
ith other minerals, tissue manganese (Mn), zinc (Zn), copper (Cu), and
iron (Fe) were examined. For 20 wk, 40 weanling animals were fed eith
er a Cr-deficient (<0.06 mu g Cr/g diet, -Cr) or a Cr-adequate (2 mu g
Cr from CrCl3/g diet, +Cr) casein-based diet and were given 1 mg asco
rbate/d (-C) or 10 mg ascorbate/d (+C) for 20 wk. Animals fed the Cr-d
epleted diet had decreased weight at 20 wk (p < 0.01). Six hours befor
e necropsy, animals were dosed by micropipette with 1.8 mu Ci of L-[ca
rboxyl-C-14] ascorbic acid and placed in metabolic cages. Ascorbate su
pplementation increased Fe concentrations in most analyzed tissues, he
patic C-14, tissue ascorbate and Mn concentration in the adrenal and t
estes; but decreased the concentrations of Cu in the kidney and Mn in
the spleen. Liver Mn concentration was higher and kidney Mn concentrat
ion was lower in +Cr animals. Interactions between Cr and ascorbic aci
d affected Mn concentrations in bone and brain. These results indicate
that ascorbate and Cr may affect Mn distribution. Chromium supplement
ation decreased plasma cortisol, brain C-14 and the amount of C-14 exp
ired as carbon dioxide. These findings suggest that dietary Cr may aff
ect ascorbic acid metabolism and the metabolic response to stress.