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J. Nutr. First published June 17, 2009; doi:10.3945/jn.109.105114
Journal of Nutrition, doi:10.3945/jn.109.105114
Vol. 139, No. 8, 1480-1486, August 2009

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© 2009 American Society for Nutrition


Nutrient Physiology, Metabolism, and Nutrient-Nutrient Interactions

A Minute Dose of 14C-β-Carotene Is Absorbed and Converted to Retinoids in Humans1–3,

Charlene C. Ho4, Fabiana F. de Moura4, Seung-Hyun Kim4, Betty J. Burri4,5 and Andrew J. Clifford4,*

4 Department of Nutrition, University of California, Davis, CA 95616-8669 and 5 Western Human Nutrition Research Center, Davis, CA 95616-8669

Our objective was to quantify the absorption and conversion to retinoids of a 1.01-nmol, 3.7-kBq oral dose of 14C-β-carotene in 8 healthy adults. The approach was to quantify, using AMS, the elimination of 14C in feces for up to 16 d after dosing and in urine for up to 30 d after dosing. The levels of total 14C in undiluted serial plasma samples were measured for up to 166 d after dosing. Also, the levels of 14C in the retinyl ester (RE), retinol (ROH), and β-carotene fractions that were isolated from undiluted plasma using HPLC were measured. The apparent digestibility of the 14C was 53 ± 13% (mean ± SD), based on the mass balance data, and was generally consistent with the area under the curve for zero to infinite period of 14C that was eliminated in the feces collections made up to 7.5 d after dosing. Metabolic fecal elimination, calculated as the slope per day (% 14C-dose/collection from d 7.5 to the final day), was only 0.05 ± 0.02%. The portion of the 14C dose eliminated via urine was variable (6.5 ± 5.2%). Participants [except participant 6 (P6)] had a distinct plasma peak of 14C at 0.25 d post-dose, preceded by a shoulder at ~0.1 d, and followed by a broad 14C peak that became indistinguishable from baseline at ~40 d. Plasma 14C-RE accounted for most of the absorbed 14C early after dosing and P1 had the longest delay in the first appearance of 14C-RE in plasma. The data suggest that plasma RE should be considered in estimating the ROH activity equivalent of ingested β-carotene.


* To whom correspondence should be addressed. E-mail: ajclifford{at}ucdavis.edu.

Manuscript received 27 January 2009. Initial review completed 13 February 2009. Revision accepted 24 May 2009.

Published online 17 June 2009.







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