Kohlschütter A, Mayatepek E, Finckh B, Hübner C
University Children's Hospital, Hamburg, Germany.
J Inherit Metab Dis. 1997 Aug;20(4):581-6. doi: 10.1023/a:1005311227094.
Studying the biological effects of vitamin e in humans is difficult because conditions involving vitamin E deficiency are usually associated with chronic multiple pathology. Genetic vitamin E deficiency caused by a deficient alpha-tocopherol transport protein offers unique possibilities for study of vitamin E effects since the patients can be studied in good general health. In such a patient we manipulated plasma alpha-tocopherol levels in a wide range by varying oral alpha-tocopherol supplements and measured urinary leukotriene E4 (LTE4) concentrations. LTE4 excretion proved inversely correlated to plasma alpha-tocopherol levels. This strongly suggests that in genetic vitamin E deficiency, alpha-tocopherol influences formation of leukotrienes in vivo.
研究维生素E对人体的生物学效应颇具难度,因为与维生素E缺乏相关的情况通常伴有慢性多种病理状况。由α-生育酚转运蛋白缺乏引起的遗传性维生素E缺乏为研究维生素E的效应提供了独特的研究机会,因为这些患者总体健康状况良好,便于进行研究。在这样一名患者中,我们通过改变口服α-生育酚补充剂的剂量,在较大范围内调节血浆α-生育酚水平,并测定尿白三烯E4(LTE4)浓度。结果证明,LTE4排泄与血浆α-生育酚水平呈负相关。这有力地表明,在遗传性维生素E缺乏症中,α-生育酚在体内影响白三烯的形成。