Suppression of Amyloid-β Adsorption on Endoplasmic Reticulum Stress-Mimicking Membranes by α-Tocopherol and α-Tocotrienol

J Phys Chem Lett. 2022 Dec 29;13(51):11955-11960. doi: 10.1021/acs.jpclett.2c03098. Epub 2022 Dec 19.

Abstract

Two forms of hydrophobic vitamin E (VE), α-tocopherol (Toc) and α-tocotrienol (Toc3), have been proposed to be effective against Alzheimer's disease (AD), the etiology of which is thought to involve endoplasmic reticulum (ER) stress. However, previous studies reported conflicting effects of Toc and Toc3 on the risk of AD. We prepared liposomes mimicking the phase separation of the ER membrane (solid-ordered/liquid-disordered phase separation) and studied how VE can influence the interaction between amyloid-β (Aβ) and the ER membrane. We found that Toc could inhibit the formation of the solid-ordered phase more significantly than Toc3. Furthermore, Aβ protofibril adsorption on ER stress-mimicking membranes was more strongly suppressed by Toc compared with Toc3. Therefore, we concluded that VE can relieve ER stress by destabilizing the solid-ordered phase of the ER membrane and subsequently reducing the amount of Aβ adsorbed on the membrane. Moreover, Toc exerted a stronger effect than Toc3.

MeSH terms

  • Adsorption
  • Alzheimer Disease*
  • Amyloid beta-Peptides
  • Endoplasmic Reticulum Stress
  • Humans
  • Tocotrienols*
  • Vitamin E / pharmacology
  • alpha-Tocopherol / pharmacology

Substances

  • alpha-Tocopherol
  • tocotrienol, alpha
  • Tocotrienols
  • Vitamin E
  • Amyloid beta-Peptides