Recent advances in vitamin E metabolism and deficiency

被引:38
作者
Eggermont, Ephrem [1 ]
机构
[1] Univ Hosp Gasthuisberg, Dept Pediat, B-3000 Louvain, Belgium
关键词
alpha-tocopherol transfer protein; AVED; selective vitamin E deficiency; tocopherol; vitamin E;
D O I
10.1007/s00431-006-0084-5
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Alpha-, beta-, gamma- and delta-tocopherol are present in many foods and are, in the absence of fat malabsorption, well absorbed from the gut. Their anti-oxidant property is well known and protects arteries and capillaries as well as blood lipids and nervous tissue against oxidative stress. In contrast to beta-, gamma- and delta-tocopherol, alpha-tocopherol is preferentially conserved by the discriminating action of the liver alpha-tocopherol transfer protein, which also maintains plasma alpha-tocopherol concentration within a range of 20 to 40 mu M. In the circulation, alpha-tocopherol, in association with the transfer-protein, is assembled into the very low-density lipoprotein and low-density liprotein particles and released for use by the peripheral tissues. Recent data suggest that alpha-tocopherol is not only an anti-oxidant but also a regulator of gene expression through its binding to nuclear receptors. The precise mechanism of regulating gene expression, however, is still unknown. The four tocopherols are ultimately degraded by omega-oxidation and subsequent beta-oxidations followed by the elimination of the metabolites in the bile and in the urine. Patients with a defect of the alpha-tocopherol transfer protein are unable to maintain their alpha-tocopherol reserves and progressively lose tendon reflexes and have signs and symptoms of spinocerebellar ataxia while plasma vitamin E level drops below 2 mu g/ml.
引用
收藏
页码:429 / 434
页数:6
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