Vitamin E: Not only a single stereoisomer

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • M. Eggersdorfer
  • K. Schmidt
  • S. Péter
  • J. Richards
  • B. Winklhofer-Roob
  • A. Hahn
  • U. Obermüller-Jevic

Externe Organisationen

  • Reichsuniversität Groningen
  • Eberhard Karls Universität Tübingen
  • Universität Graz
  • BASF SE
  • dsm-firmenich
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Seiten (von - bis)106-111
Seitenumfang6
FachzeitschriftFree Radical Biology and Medicine
Jahrgang215
Frühes Online-Datum23 Feb. 2024
PublikationsstatusVeröffentlicht - März 2024

Abstract

The recent publication by Azzi and colleagues puts forth the argument that only RRR-α-tocopherol should be considered as vitamin E from a physiological point of view. They base their argument primarily on the assertion that only this form has been used to treat stark vitamin E deficiency in humans (known as AVED, or Ataxia with Vitamin E Deficiency). Azzi et al. also argue that other chemically similar molecules, such as tocopherols other than α-tocopherol and tocotrienols do not provide vitamin E activity. Azzi and colleagues are correct on this second point. An investigation into the biological activities of vitamin E, and the mechanisms behind these activities, confirms that physiological vitamin E activity is limited to certain α-tocopherol forms. However, it is also clear that these activities are not restricted only to the RRR-form but include other 2R-forms as well. Indeed, the α-tocopherol transfer protein (α-TTP), which is critical to mediate vitamin E trafficking and biological activity, and genetic defects of which lead to vitamin E deficiency, binds well to all 2R-forms of α-tocopherol. Furthermore, both RRR-α-tocopherol and the other 2R-forms are maintained in human plasma and distributed to tissues and organs, whereas the 2S-stereoisomers are excreted quickly. As such, in recent years the definition of vitamin E including both 2R- and RRR-α-tocopherol has gained both broad scientific and regulatory acceptance. Consistent with this understanding, we provide evidence that AVED has indeed been treated successfully with forms in addition to RRR-α-tocopherol, again arguing against the restriction of the definition to RRR-α-tocopherol only. Finally, we provide evidence against any safety concerns utilizing the currently accepted definition of vitamin E.

ASJC Scopus Sachgebiete

Zitieren

Vitamin E: Not only a single stereoisomer. / Eggersdorfer, M.; Schmidt, K.; Péter, S. et al.
in: Free Radical Biology and Medicine, Jahrgang 215, 03.2024, S. 106-111.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Eggersdorfer, M, Schmidt, K, Péter, S, Richards, J, Winklhofer-Roob, B, Hahn, A & Obermüller-Jevic, U 2024, 'Vitamin E: Not only a single stereoisomer', Free Radical Biology and Medicine, Jg. 215, S. 106-111. https://doi.org/10.1016/j.freeradbiomed.2024.02.013
Eggersdorfer, M., Schmidt, K., Péter, S., Richards, J., Winklhofer-Roob, B., Hahn, A., & Obermüller-Jevic, U. (2024). Vitamin E: Not only a single stereoisomer. Free Radical Biology and Medicine, 215, 106-111. https://doi.org/10.1016/j.freeradbiomed.2024.02.013
Eggersdorfer M, Schmidt K, Péter S, Richards J, Winklhofer-Roob B, Hahn A et al. Vitamin E: Not only a single stereoisomer. Free Radical Biology and Medicine. 2024 Mär;215:106-111. Epub 2024 Feb 23. doi: 10.1016/j.freeradbiomed.2024.02.013
Eggersdorfer, M. ; Schmidt, K. ; Péter, S. et al. / Vitamin E : Not only a single stereoisomer. in: Free Radical Biology and Medicine. 2024 ; Jahrgang 215. S. 106-111.
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AU - Eggersdorfer, M.

AU - Schmidt, K.

AU - Péter, S.

AU - Richards, J.

AU - Winklhofer-Roob, B.

AU - Hahn, A.

AU - Obermüller-Jevic, U.

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