CHAPTER 16. Essentiality, Bioavailability, and Health Benefits of α-Tocopherol Stereoisomers

R. Bruno
{"title":"CHAPTER 16. Essentiality, Bioavailability, and Health Benefits of α-Tocopherol Stereoisomers","authors":"R. Bruno","doi":"10.1039/9781788016216-00228","DOIUrl":null,"url":null,"abstract":"Vitamin E is the term that describes eight structurally-related vitamers, specifically four tocopherols (α-, β-, γ-, and δ-) and four tocotrienols (α-, β-, γ-, and δ-). Although each vitamer has antioxidant activity that prevents the cyclic progression of lipid peroxidation, α-tocopherol is the only form that is essential for humans because it prevents and reverses clinical deficiency of vitamin E. These vitamers also differ substantially in their bioavailability, which results in α-tocopherol accumulating to the greatest extent in the circulation and tissues in humans. In nature, α-tocopherol exists as a single stereoisomer (2R, 4′R, 8′R- or RRR-α-tocopherol) whereas most dietary supplements and fortified foods contain an all racemic mixture of eight α-tocopherol stereoisomers. Importantly, only 50% of these stereoisomers are appreciably bioavailable, and therefore capable of contributing to dietary α-tocopherol requirements in humans. This chapter will therefore focus on the bioavailability, metabolism, and trafficking of vitamin E forms along the gut–liver axis. It will also discuss their structure–function aspects concerning their ability to contribute to dietary vitamin E requirements and associated health benefits.","PeriodicalId":23674,"journal":{"name":"Vitamin E","volume":"21 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-02-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Vitamin E","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/9781788016216-00228","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

Abstract

Vitamin E is the term that describes eight structurally-related vitamers, specifically four tocopherols (α-, β-, γ-, and δ-) and four tocotrienols (α-, β-, γ-, and δ-). Although each vitamer has antioxidant activity that prevents the cyclic progression of lipid peroxidation, α-tocopherol is the only form that is essential for humans because it prevents and reverses clinical deficiency of vitamin E. These vitamers also differ substantially in their bioavailability, which results in α-tocopherol accumulating to the greatest extent in the circulation and tissues in humans. In nature, α-tocopherol exists as a single stereoisomer (2R, 4′R, 8′R- or RRR-α-tocopherol) whereas most dietary supplements and fortified foods contain an all racemic mixture of eight α-tocopherol stereoisomers. Importantly, only 50% of these stereoisomers are appreciably bioavailable, and therefore capable of contributing to dietary α-tocopherol requirements in humans. This chapter will therefore focus on the bioavailability, metabolism, and trafficking of vitamin E forms along the gut–liver axis. It will also discuss their structure–function aspects concerning their ability to contribute to dietary vitamin E requirements and associated health benefits.
第十六章。α-生育酚立体异构体的必要性、生物利用度和健康益处
维生素E是描述八种结构相关的维生素的术语,特别是四种生育酚(α-, β-, γ-和δ-)和四种生育三烯醇(α-, β-, γ-和δ-)。尽管每种维生素都具有抗氧化活性,可以防止脂质过氧化循环的进行,但α-生育酚是人类唯一必需的维生素,因为它可以预防和逆转维生素e的临床缺乏症。这些维生素在生物利用度上也存在很大差异,这导致α-生育酚在人体循环和组织中最大程度地积累。在自然界中,α-生育酚以单一的立体异构体存在(2R, 4'R, 8'R -或RRR-α-生育酚),而大多数膳食补充剂和强化食品都含有八种α-生育酚立体异构体的外消旋混合物。重要的是,这些立体异构体中只有50%具有明显的生物利用度,因此能够满足人类饮食中α-生育酚的需求。因此,本章将着重于生物利用度、代谢和维生素E形式沿肠-肝轴的运输。它还将讨论它们的结构-功能方面,涉及它们对膳食维生素E需求的贡献以及相关的健康益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信