Review
Copyright ©The Author(s) 2016. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Biol Chem. Feb 26, 2016; 7(1): 14-43
Published online Feb 26, 2016. doi: 10.4331/wjbc.v7.i1.14
Complexity of vitamin E metabolism
Lisa Schmölz, Marc Birringer, Stefan Lorkowski, Maria Wallert
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
Marc Birringer, Department of Nutritional, Food and Consumer Studies, University of Applied Sciences, 36037 Fulda, Germany
Author contributions: Schmölz L, Birringer M, Lorkowski S and Wallert M drafted parts of the manuscript; Birringer M and Lorkowski S revised it critically; Lorkowski S and Wallert M contributed equally.
Supported by Grants from “Forschung für die Praxis “of the Hessisches Ministerium für Wissenschaft und Kunst to Birringer M; and grants from the Federal Ministry of Education and Research and the Deutsche Forschungsgemeinschaft to Lorkowski S as an acknowledgement to the national institutions that currently support our research in the field of vitamin E and its long-chain metabolites.
Conflict-of-interest statement: Authors declare no conflict of interests for this article.
Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Correspondence to: Stefan Lorkowski, PhD, 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, Dornburger Straße 25, 07743 Jena, Germany. stefan.lorkowski@uni-jena.de
Telephone: +49-3641-949710 Fax: +49-3641-949712
Received: August 24, 2015
Peer-review started: August 27, 2015
First decision: October 27, 2015
Revised: November 25, 2015
Accepted: January 16, 2016
Article in press: January 19, 2016
Published online: February 26, 2016
Abstract

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.

Keywords: Vitamin E metabolism, Long-chain metabolites of vitamin E, Vitamin E bioavailability, Vitamin E transport

Core tip: Several factors influence vitamin E bioavailability. Gender, age and genetic constitution cannot be modified but life-style and vitamin E intake can be. Physiological handling of vitamin E involves intestinal absorption, vascular transport, hepatic sorting by intracellular binding proteins, and hepatic metabolism. These processes involve kinetics which vary between the different vitamin E forms. The coordinated metabolism of vitamin E is an effective physiological pathway to prevent excessive accumulation of non-α-tocopherol forms. Interactions with other nutrients or pharmaceutics occur. To evaluate vitamin E status, analytical procedures to detect and quantify vitamin E and metabolites are crucial. Current state-of-the-art analytics are presented.