J. Lipid Res. Acyl Labeled PIP's available August 1, 2008
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Journal of Lipid Research, Vol. 41, 1790-1800, November 2000
Copyright © 2000 by Lipid Research, Inc.


Original Article

Long-term kinetic study of ß-carotene, using accelerator mass spectrometry in an adult volunteer

Stephen R. Duekera, Yumei Lina, Bruce A. Buchholzd, Phillip D. Schneiderc, Michael W. Laméb, H. J. Segallb, John S. Vogela,d, and Andrew J. Clifforda
a Department of Nutrition, University of California, Davis, CA 95616
b Department of Molecular Biosciences, University of California, Davis, CA 95616
c Cancer Center, University of California Davis Medical Center, Sacramento, CA 95817
d Center for Accelerator Mass Spectrometry, Lawrence Livermore National Laboratory, Livermore, CA 94551

Correspondence to: Stephen R. Dueker

We present a sensitive tracer method, suitable for in vivo human research, that uses ß-[14C]carotene coupled with accelerator mass spectrometry (AMS) detection. Using this approach, the concentration-time course of a physiological (306 µg; 200 nCi) oral dose of ß-[14C]carotene was determined for 209 days in plasma. Analytes included ß-[14C]carotene, [14C]retinyl esters, [14C]retinol, and several [14C]retinoic acids. There was a 5.5-h lag between dosing and the appearance of 14C in plasma. Labeled ß-carotene and [14C]retinyl esters rose and displayed several maxima with virtually identical kinetic profiles over the first 24-h period; elevated [14C]retinyl ester concentrations were sustained in the plasma compartment for >21 h postdosing. The appearance of [14C]retinol in plasma was also delayed 5.5 h postdosing and its concentration rose linearly for 28 h before declining. Cumulative urine and stool were collected for 17 and 10 days, respectively, and 57.4% of the dose was recovered in the stool within 48 h postdosing. The stool was the major excretion route for the absorbed dose. The turnover times (1/kel) for ß-carotene and retinol were 58 and 302 days, respectively. Area under the curve analysis of the plasma response curves suggested a molar vitamin A value of 0.53 for ß-carotene, with a minimum of 62% of the absorbed ß-carotene being cleaved to vitamin A.

In summary, AMS is an excellent tool for defining the in vivo metabolic behavior of ß-carotene and related compounds at physiological concentrations. Further, our data suggest that retinyl esters derived from ß-carotene may undergo hepatic resecretion with VLDL in a process similar to that observed for ß-carotene. Dueker, S. R., Y. Lin, B. A. Buchholz, P. D. Schneider, M. W. Lamé, H. J. Segall, J. S. Vogel, and A. J. Clifford. Long-term kinetic study of ß-carotene, using accelerator mass spectrometry in an adult volunteer. J. Lipid Res. 2000. 41: 1790;–1800.

Supplementary key words: vitamin A, human, isotope


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