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α-生育酚不会加速大鼠体内γ-生育酚和生育三烯酚的消耗,也不会加速它们代谢物的排泄。

α-Tocopherol does not accelerate depletion of γ-tocopherol and tocotrienol or excretion of their metabolites in rats.

作者信息

Uchida Tomono, Nomura Saki, Sakuma Eri, Hanzawa Fumiaki, Ikeda Saiko

机构信息

Department of Home Economics, Aichi Gakusen University, Okazaki, Japan.

出版信息

Lipids. 2013 Jul;48(7):687-95. doi: 10.1007/s11745-013-3796-0. Epub 2013 May 23.

DOI:10.1007/s11745-013-3796-0
PMID:23700248
Abstract

From an enzyme kinetic study using rat liver microsomes, α-tocopherol has been suggested to accelerate the other vitamin E catabolism by stimulating vitamin E ω-hydroxylation, the late limiting reaction of the vitamin E catabolic pathway. To test the effect of α-tocopherol on catabolism of the other vitamin E isoforms in vivo, we determined whether α-tocopherol accelerates depletion of γ-tocopherol and tocotrienol and excretion of their metabolites in rats. Male Wistar rats were fed a γ-tocopherol-rich diet for 6 weeks followed by a γ-tocopherol-free diet with or without α-tocopherol for 7 days. Intake of γ-tocopherol-free diets lowered γ-tocopherol concentrations in serum, liver, adrenal gland, small intestine, and heart, but there was no effect of dietary α-tocopherol on γ-tocopherol concentrations. The level of urinary excretion of γ-tocopherol metabolite was not affected by dietary α-tocopherol. Next, the effect of α-tocopherol on tocotrienol depletion was examined using rats fed a tocotrienol-rich diet for 6 weeks. Subsequent intake of a tocotrienol-free diet with or without α-tocopherol for 7 days depleted concentrations of α- and γ-tocotrienol in serum and tissues, which was accompanied by a decrease in the excretion of γ-tocotrienol metabolite. However, neither the tocotrienol concentration nor γ-tocotrienol metabolite excretion was affected by dietary α-tocopherol. These data showed that dietary α-tocopherol did not accelerate the depletion of γ-tocopherol and tocotrienol and their metabolite excretions, suggesting that the positive effect of α-tocopherol on vitamin E ω-hydroxylase is not sufficient to affect the other isoform concentrations in tissues.

摘要

通过使用大鼠肝脏微粒体进行的酶动力学研究表明,α-生育酚可通过刺激维生素E ω-羟化作用来加速其他维生素E的分解代谢,维生素E ω-羟化作用是维生素E分解代谢途径中的晚期限速反应。为了测试α-生育酚在体内对其他维生素E异构体分解代谢的影响,我们确定了α-生育酚是否会加速大鼠体内γ-生育酚和生育三烯酚的消耗及其代谢产物的排泄。雄性Wistar大鼠先喂食富含γ-生育酚的饮食6周,然后喂食不含γ-生育酚的饮食7天,该饮食中添加或不添加α-生育酚。摄入不含γ-生育酚的饮食会降低血清、肝脏、肾上腺、小肠和心脏中的γ-生育酚浓度,但饮食中的α-生育酚对γ-生育酚浓度没有影响。γ-生育酚代谢产物的尿排泄水平不受饮食中α-生育酚的影响。接下来,使用喂食富含生育三烯酚饮食6周的大鼠研究了α-生育酚对生育三烯酚消耗的影响。随后摄入不含生育三烯酚的饮食7天,无论是否添加α-生育酚,都会使血清和组织中α-和γ-生育三烯酚的浓度降低,同时γ-生育三烯酚代谢产物的排泄也会减少。然而,饮食中的α-生育酚对生育三烯酚浓度和γ-生育三烯酚代谢产物排泄均无影响。这些数据表明,饮食中的α-生育酚不会加速γ-生育酚和生育三烯酚的消耗及其代谢产物的排泄,这表明α-生育酚对维生素E ω-羟化酶的积极作用不足以影响组织中其他异构体的浓度。

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Disruption of mouse cytochrome p450 4f14 (Cyp4f14 gene) causes severe perturbations in vitamin E metabolism.敲除小鼠细胞色素 P450 4f14(Cyp4f14 基因)导致维生素 E 代谢严重紊乱。
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γ-和δ-生育三烯酚对肥胖及代谢并发症的调控作用
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