Schmölz Lisa, Birringer Marc, Lorkowski Stefan, Wallert Maria
Lisa Schmölz, Stefan Lorkowski, Maria Wallert, Department of Nutritional Biochemistry and Physiology, Institute of Nutrition, Friedrich Schiller University Jena, Germany and Competence Center for Nutrition and Cardiovascular Health, Halle-Jena-Leipzig, 07743 Jena, Germany.
World J Biol Chem. 2016 Feb 26;7(1):14-43. doi: 10.4331/wjbc.v7.i1.14.
Bioavailability of vitamin E is influenced by several factors, most are highlighted in this review. While gender, age and genetic constitution influence vitamin E bioavailability but cannot be modified, life-style and intake of vitamin E can be. Numerous factors must be taken into account however, i.e., when vitamin E is orally administrated, the food matrix may contain competing nutrients. The complex metabolic processes comprise intestinal absorption, vascular transport, hepatic sorting by intracellular binding proteins, such as the significant α-tocopherol-transfer protein, and hepatic metabolism. The coordinated changes involved in the hepatic metabolism of vitamin E provide an effective physiological pathway to protect tissues against the excessive accumulation of, in particular, non-α-tocopherol forms. Metabolism of vitamin E begins with one cycle of CYP4F2/CYP3A4-dependent ω-hydroxylation followed by five cycles of subsequent β-oxidation, and forms the water-soluble end-product carboxyethylhydroxychroman. All known hepatic metabolites can be conjugated and are excreted, depending on the length of their side-chain, either via urine or feces. The physiological handling of vitamin E underlies kinetics which vary between the different vitamin E forms. Here, saturation of the side-chain and also substitution of the chromanol ring system are important. Most of the metabolic reactions and processes that are involved with vitamin E are also shared by other fat soluble vitamins. Influencing interactions with other nutrients such as vitamin K or pharmaceuticals are also covered by this review. All these processes modulate the formation of vitamin E metabolites and their concentrations in tissues and body fluids. Differences in metabolism might be responsible for the discrepancies that have been observed in studies performed in vivo and in vitro using vitamin E as a supplement or nutrient. To evaluate individual vitamin E status, the analytical procedures used for detecting and quantifying vitamin E and its metabolites are crucial. The latest methods in analytics are presented.
维生素E的生物利用度受多种因素影响,本综述重点介绍了其中的大部分因素。虽然性别、年龄和基因构成会影响维生素E的生物利用度,但无法改变,而生活方式和维生素E的摄入量则可以改变。然而,必须考虑众多因素,例如,口服维生素E时,食物基质可能含有竞争性营养素。复杂的代谢过程包括肠道吸收、血管运输、肝脏通过细胞内结合蛋白(如重要的α-生育酚转运蛋白)进行分类以及肝脏代谢。维生素E肝脏代谢中涉及的协同变化提供了一条有效的生理途径,以保护组织免受特别是非α-生育酚形式的过度积累。维生素E的代谢始于一个由CYP4F2/CYP3A4依赖性ω-羟基化的循环,随后是五个后续β-氧化的循环,并形成水溶性终产物羧乙基羟基色满。所有已知的肝脏代谢产物都可以结合,并根据其侧链长度通过尿液或粪便排出。维生素E的生理处理是动力学的基础,不同维生素E形式之间的动力学有所不同。在此,侧链的饱和度以及色满环系统的取代也很重要。与维生素E相关的大多数代谢反应和过程也与其他脂溶性维生素共享。本综述还涵盖了与其他营养素(如维生素K)或药物的相互作用影响。所有这些过程调节维生素E代谢产物的形成及其在组织和体液中的浓度。代谢差异可能是体内和体外使用维生素E作为补充剂或营养素的研究中观察到差异的原因。为了评估个体维生素E状态,用于检测和定量维生素E及其代谢产物的分析程序至关重要。本文介绍了最新的分析方法。