Reboul E, Thap S, Perrot E, Amiot M-J, Lairon D, Borel P
INSERM, U476 Nutrition Humaine et Lipides, Marseille, France.
Eur J Clin Nutr. 2007 Oct;61(10):1167-73. doi: 10.1038/sj.ejcn.1602635. Epub 2007 Jan 31.
(R,R,R)-alpha-tocopherol is a fat-soluble antioxidant vitamin generally ingested with other dietary antioxidants. The objective of this study was to assess whether the main dietary antioxidant classes, that is carotenoids, polyphenols, vitamin C and gamma-tocopherol, affect the intestinal absorption of alpha-tocopherol. METHODS, DESIGN AND SUBJECTS: We evaluated first the effect of different combinations of antioxidants on (R,R,R)-alpha-tocopherol absorption by a human intestinal cell line (Caco-2 clone TC7). Then we compared the effect of two doses of a dietary antioxidant (lutein) on the postprandial chylomicron alpha-tocopherol responses to an alpha-tocopherol-rich meal. Eight healthy men ate two similar meals in a random order at a 1 month interval. The meals contained 24 mg alpha-tocopherol in sunflower oil plus either 18 or 36 mg lutein. Blood samples were collected during the postprandial periods to compare chylomicron alpha-tocopherol responses.
A mixture of polyphenols (gallic acid, caffeic acid, (+)-catechin and naringenin) and a mixture of carotenoids (lycopene, beta-carotene and lutein) significantly impaired alpha-tocopherol absorption in Caco-2 cells (P<0.001 and P<0.0001, respectively). The inhibitory effect of gamma-tocopherol was close to significance (P=0.055). In contrast, vitamin C had no significant effect (P=0.158). Naringenin was the only polyphenol that significantly impaired alpha-tocopherol absorption. Postprandial alpha-tocopherol response was weakest at the highest dose of lutein (616+/-280 nmol/l h vs 1001+/-287 nmol/l h). The observed extent of reduction (-38%, P=0.069) supported the inhibitory effect of carotenoids observed in the Caco-2 experiments.
Naringenin, carotenoids and probably gamma-tocopherol can impair alpha-tocopherol absorption whereas vitamin C and phenolic acids have no effect.
(R,R,R)-α-生育酚是一种脂溶性抗氧化维生素,通常与其他膳食抗氧化剂一起摄入。本研究的目的是评估主要的膳食抗氧化剂类别,即类胡萝卜素、多酚、维生素C和γ-生育酚,是否会影响α-生育酚的肠道吸收。
方法、设计与研究对象:我们首先通过人肠细胞系(Caco-2克隆TC7)评估了不同抗氧化剂组合对(R,R,R)-α-生育酚吸收的影响。然后我们比较了两种剂量的膳食抗氧化剂(叶黄素)对富含α-生育酚餐食的餐后乳糜微粒α-生育酚反应的影响。八名健康男性以随机顺序在1个月的间隔内食用两顿相似的餐食。餐食包含24毫克葵花籽油中的α-生育酚,外加18毫克或36毫克叶黄素。在餐后期间采集血样以比较乳糜微粒α-生育酚反应。
多酚混合物(没食子酸、咖啡酸、(+)-儿茶素和柚皮素)和类胡萝卜素混合物(番茄红素、β-胡萝卜素和叶黄素)显著损害了Caco-2细胞中α-生育酚的吸收(分别为P<0.001和P<0.0001)。γ-生育酚的抑制作用接近显著水平(P=0.055)。相比之下,维生素C没有显著影响(P=0.158)。柚皮素是唯一显著损害α-生育酚吸收的多酚。餐后α-生育酚反应在叶黄素最高剂量时最弱(616±280纳摩尔/升·小时对1001±287纳摩尔/升·小时)。观察到的降低程度(-38%,P=0.069)支持了在Caco-2实验中观察到的类胡萝卜素的抑制作用。
柚皮素、类胡萝卜素以及可能的γ-生育酚会损害α-生育酚的吸收,而维生素C和酚酸则没有影响。