Tocotrienols: Vitamin E beyond tocopherols

被引:426
作者
Sen, CK [1 ]
Khanna, S [1 ]
Roy, S [1 ]
机构
[1] Ohio State Univ, Med Ctr, Davis Heart & Lung Res Inst 512, Lab Mol Med,Dept Surg, Columbus, OH 43210 USA
关键词
antioxidant; redox; nutrient; supplement; neuroprotection;
D O I
10.1016/j.lfs.2005.12.001
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
In nature, eight substances have been found to have vitamin E activity: alpha-, beta-, gamma- and delta-tocopherol; and alpha-, beta-, gamma- and delta-tocotrienol. Yet, of all papers on vitamin E listed in PubMed less than 1% relate to tocotrienols. The abundance of alpha-tocopherol in the human body and the comparable efficiency of all vitamin E molecules as antioxidants, led biologists to neglect the non-tocopherol vitamin E molecules as topics for basic and clinical research. Recent developments warrant a serious reconsideration of this conventional wisdom. Tocotrienols possess powerful neuroprotective, anti-cancer and cholesterol lowering properties that are often not exhibited by tocopherols. Current developments in vitamin E research clearly indicate that members of the vitamin E family are not redundant with respect to their biological functions. alpha-Tocotrienol, gamma-tocopherol, and delta-tocotrienol have emerged as vitamin E molecules with functions in health and disease that are clearly distinct from that of alpha-tocopherol. At nanomolar concentration, alpha-tocotrienol, not alpha-tocopherol, prevents neurodegeneration. On a concentration basis, this finding represents the most potent of all biological functions exhibited by any natural vitamin E molecule. An expanding body of evidence support that members of the vitamin E family are functionally unique. In recognition of this fact, title claims in manuscripts should be limited to the specific form of vitamin E studied. For example, evidence for toxicity of a specific form of tocopherol in excess may not be used to conclude that high dosage "vitamin E" supplementation may increase all-cause mortality. Such conclusion incorrectly implies that tocotrienols are toxic as well under conditions where tocotrienols were not even considered. The current state of knowledge warrants strategic investment into the lesser known forms of vitamin E. This will enable prudent selection of the appropriate vitamin E molecule for studies addressing a specific need. (c) 2006 Published by Elsevier Inc.
引用
收藏
页码:2088 / 2098
页数:11
相关论文
共 147 条
[51]  
Liebecq C, 1992, IUPAC IUBMB JOINT CO
[52]  
Liede K, 1998, Oral Dis, V4, P78
[53]   α- and γ-tocotrienols are metabolized to carboxyethyl-hydroxychroman derivatives and excreted in human urine [J].
Lodge, JK ;
Ridlington, J ;
Leonard, S ;
Vaule, H ;
Traber, MG .
LIPIDS, 2001, 36 (01) :43-48
[54]   Antiproliferative and apoptotic effects of tocopherols and tocotrienols on preneoplastic and neoplastic mouse mammary epithelial cells [J].
McIntyre, BS ;
Briski, KP ;
Gapor, A ;
Sylvester, PW .
PROCEEDINGS OF THE SOCIETY FOR EXPERIMENTAL BIOLOGY AND MEDICINE, 2000, 224 (04) :292-301
[55]   Antiproliferative and apoptotic effects of tocopherols and tocotrienols on normal mouse mammary epithelial cells [J].
McIntyre, BS ;
Briski, KP ;
Tirmenstein, MA ;
Fariss, MW ;
Gapor, A ;
Sylvester, PW .
LIPIDS, 2000, 35 (02) :171-180
[56]  
MCKEOWNEYSSEN G, 1988, CANCER RES, V48, P4701
[57]  
Mensink RP, 1999, AM J CLIN NUTR, V69, P213
[58]   Meta-analysis: High-dosage vitamin E supplementation may increase all-cause mortality [J].
Miller, ER ;
Pastor-Barriuso, R ;
Dalal, D ;
Riemersma, RA ;
Appel, LJ ;
Guallar, E .
ANNALS OF INTERNAL MEDICINE, 2005, 142 (01) :37-46
[59]   UVB photoprotection with antioxidants:: Effects of oral therapy with d-α-tocopherol and ascorbic acid on the minimal erythema dose [J].
Mireles-Rocha, H ;
Galindo, I ;
Huerta, M ;
Trujillo-Hernández, B ;
Elizalde, A ;
Cortés-Franco, R .
ACTA DERMATO-VENEREOLOGICA, 2002, 82 (01) :21-24
[60]   Vitamin E isoforms α-tocotrienol and γ-tocopherol prevent cerebral infarction in mice [J].
Mishima, K ;
Tanaka, T ;
Pu, FL ;
Egashira, N ;
Iwasaki, K ;
Hidaka, R ;
Matsunaga, K ;
Takata, J ;
Karube, Y ;
Fujiwara, M .
NEUROSCIENCE LETTERS, 2003, 337 (01) :56-60