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The Journal of Lipid Research, Vol. 39, 2250-2260, November 1998
Copyright © 1998 by Lipid Research, Inc.


Original Article

Low and high responders to pharmacological doses of ß-carotene: proportion in the population, mechanisms involved and consequences on ß-carotene metabolism

Patrick Borela, Pascal Groliera, Nadia Mekkib, Yves Boiriec, Yvanne Rochettea, Brigitte Le Royd, Marie C. Alexandre-Gouabaua, Denis Laironb, and Véronique Azais-Braescoa
a Unité des Maladies Métaboliques et des Micronutriments, INRA Clermont-Ferrand 63000
b U476 INSERM, Marseille 13000
c Laboratoire de Nutrition Humaine, Université d'Auvergne Clermont-Ferrand 63000
d Faculté de Pharmacie, Université de Rennes I, Rennes 35000, France

Correspondence to: Patrick Borel.

The aim of this study was to assess the interindividual variability of chylomicron ß-carotene response to a pharmacological load of ß-carotene in the population, to identify the mechanisms responsible for this variability, and to evaluate its consequences on ß-carotene status and metabolism. The variability, as estimated by the 3-h chylomicron ß-carotene response to 120 mg ß-carotene in 79 healthy male volunteers, was high (CV = 61%), but it was unimodal and all the subjects had detectable chylomicron ß-carotene. In 16 subjects randomly selected among the 79, the interindividual variability of the triglyceride-adjusted chylomicron (ß-carotene + retinyl palmitate) response (0–12.5 h area under the curve) was high (CV = 54%), suggesting that there is a high interindividual variability in the efficiency of intestinal absorption of ß-carotene. The chylomicron ß-carotene response was correlated (r = 0.50, P < 0.05) with the chylomicron triglyceride response. The ß-carotene status, as assessed by ß-carotene concentration in buccal mucosal cells, was correlated (r = 0.73, P < 0.05) with the triglyceride-adjusted chylomicron ß-carotene response, i.e., with the ability to respond to ß-carotene. The triglyceride-adjusted chylomicron retinyl-palmitate response was correlated (r = 0.55, P < 0.05) with the triglyceride-adjusted chylomicron ß-carotene response. Plasma all-trans retinoic acid slightly, but significantly, increased (+40%) 3 h after the ß-carotene load, but this increase was not related to the triglyceride-adjusted ß-carotene response.

In conclusion, the ability to respond to ß-carotene is highly variable, but there is probably a very small proportion of true non-responders to pharmacological doses of ß-carotene in the healthy population. This variability is apparently mainly due to interindividual differences in the efficiency of intestinal absorption of ß-carotene and in chylomicron metabolism. The ability to respond to ß-carotene can affect the ß-carotene status and the provitamin A activity of ß-carotene, but it has apparently no effect on the amount of retinoic acid appearing in the plasma after the ingestion of a pharmacological dose of ß-carotene.—Borel, P., P. Grolier, N. Mekki, Y. Boirie, Y. Rochette, B. Le Roy, M. C. Alexandre-Gouabau, D. Lairon, and V. Azais-Braesco. Low and high responders to pharmacological doses of ß-carotene: proportion in the population, mechanisms involved, and consequences on ß-carotene metabolism. J. Lipid Res. 1998. 39: 2250–2260.

Supplementary key words: provitamin A activity, retinoic acid, chylomicron, retinyl-palmitate, ß-carotene status, erythropoeitic protoporphyria


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