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Winklhofer-Roob, BM; Shmerling, DH; Schimek, MG; Tuchschmid, PE.
Short-term changes in erythrocyte alpha-tocopherol content of vitamin E-deficient patients with cystic fibrosis.
AMER J CLIN NUTR. 1992; 55(1): 100-103. Doi: 10.1093/ajcn/55.1.100 [OPEN ACCESS]
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Schimek Michael
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Abstract:
Polyunsaturated fatty acids of biomembranes are a major target of lipid peroxidation. In vitamin E deficiency an efficient delivery of a high oral loading dose of all-rac-alpha-tocopheryl acetate to erythrocyte membranes could provide an early onset antioxidative effect. We investigated short-term changes in erythrocyte alpha-tocopherol after a single oral dose of 100 mg all-rac-alpha-tocopheryl acetate/kg in 10 vitamin E-deficient cystic fibrosis (CF) patients. Over 24 h, erythrocyte alpha-tocopherol increased 68% to 420% of preloading concentrations. With two exceptions, peak values were achieved 12 or 24 h after administration, which was 3-18 h later than peak plasma concentrations. Separate median-based curve estimates for the changes in erythrocyte alpha-tocopherol for five patients with and five without associated cholestatic liver disease were obtained. Cross-sectional test results revealed significantly lower erythrocyte alpha-tocopherol for the 9- and 24-h observations for patients with cholestatic liver disease compared with those without. Oral all-rac-alpha-tocopheryl acetate can be rapidly incorporated into erythrocyte membranes in vitamin E-deficient CF patients.
Find related publications in this database (using NLM MeSH Indexing)
Adolescent -
Adult -
Child -
Child, Preschool -
Cholestasis, Intrahepatic - blood
Cross-Sectional Studies - blood
Cystic Fibrosis - blood
Erythrocytes - chemistry
Follow-Up Studies - chemistry
Humans - chemistry
Infant - chemistry
Random Allocation - chemistry
Vitamin E - blood
Vitamin E Deficiency - blood

Find related publications in this database (Keywords)
Erythrocyte Alpha-Tocopherol
Vitamin-E Deficiency
Cystic Fibrosis
Cholestatic Liver Disease
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