# Tocotrienols exhibit superior ferroptosis inhibition over tocopherols

**Authors:** Hao Yang, Junya Ito, Taiki Maejima, Shinnosuke Kimura, Hikaru Ino, Yusuke Hirata, Atsushi Matsuzawa, Sho Kobayashi, Eikan Mishima, Kiyotaka Nakagawa

PMC · DOI: 10.1038/s41598-025-34673-1 · Scientific Reports · 2026-01-07

## TL;DR

Tocotrienols are more effective than tocopherols at preventing ferroptosis, a type of cell death involving iron and lipid peroxidation.

## Contribution

This study reveals that tocotrienols inhibit ferroptosis more effectively than tocopherols, even at lower concentrations.

## Key findings

- Tocotrienols prevent ferroptosis at significantly lower concentrations than tocopherols.
- Tocotrienols show greater antioxidant activity in suppressing lipid peroxidation.
- Tocotrienols inhibit ferroptosis in both pharmacological and genetic models.

## Abstract

Ferroptosis is a regulated form of cell death characterized by iron-dependent phospholipid peroxidation. Micronutrients play a critical role in modulating cellular sensitivity to ferroptosis, with vitamin E being a well-known ferroptosis inhibitor through its lipophilic antioxidant property. While vitamin E naturally exists in two forms of tocochromanols, namely tocopherols and tocotrienols, each comprising α, β, γ, and δ analogs with distinct antioxidant capacities and metabolic profiles, only α-tocopherol has been the focus of most ferroptosis studies. Here, we compared the efficacy of all vitamin E analogs, including tocopherols, tocotrienols and Trolox, in terms of their ability to prevent ferroptosis and their antioxidant activities linked to suppressing lipid peroxidation. We demonstrate that tocotrienols exhibit superior ferroptosis inhibition over tocopherols. Tocotrienols prevented ferroptosis induced by both pharmacological models (inhibition of GPX4, xCT or glutathione synthesis) and a genetic model of inducible Gpx4 knockout at significantly lower concentrations than tocopherols (e.g., EC50 of 0.12 μM for α-tocotrienol and 2.0 μM for α-tocopherol in Gpx4 knockout cells). Consistent with this, tocotrienols exhibited greater antioxidant activities in suppressing lipid peroxidation. These findings highlight the distinct properties of vitamin E analogs in regulating ferroptosis and underscore the superior potential of tocotrienols as potent ferroptosis suppressors.

The online version contains supplementary material available at 10.1038/s41598-025-34673-1.

## Linked entities

- **Genes:** GPX4 (glutathione peroxidase 4) [NCBI Gene 2879], GPX4 (glutathione peroxidase 4) [NCBI Gene 2879], SLC7A11 (solute carrier family 7 member 11) [NCBI Gene 23657]
- **Chemicals:** tocotrienols (PubChem CID 9929901), tocopherols (PubChem CID 14986), Trolox (PubChem CID 40634)

## Full-text entities

- **Chemicals:** tocopherols (MESH:D024505), Tocotrienols (MESH:D024508)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12864781/full.md

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Source: https://tomesphere.com/paper/PMC12864781