# Tetraselmis chuii Supplementation Increases Skeletal Muscle Nuclear Factor Erythroid 2-Related Factor 2 and Antioxidant Enzyme Gene Expression, and Peak Oxygen Uptake in Healthy Adults: A Randomised Crossover Trial

**Authors:** Stuart P. Cocksedge, Carlos Infante, Sonia Torres, Carmen Lama, Lalia Mantecón, Manuel Manchado, Jarred P. Acton, Nehal S. Alsharif, Tom Clifford, Alex J. Wadley, Richard A. Ferguson, Nicolette C. Bishop, Neil R. W. Martin, Stephen J. Bailey

PMC · DOI: 10.3390/antiox14040435 · Antioxidants · 2025-04-03

## TL;DR

A study found that supplementing with Tetraselmis chuii, a marine microalgae, increased oxygen uptake and antioxidant gene expression in healthy adults.

## Contribution

This is the first study to show that Tetraselmis chuii supplementation improves endurance and activates antioxidant genes in humans.

## Key findings

- Tetraselmis chuii supplementation increased peak oxygen uptake (V̇O2peak) in healthy adults.
- Supplementation led to higher gene expression of antioxidant enzymes and stress-related proteins in skeletal muscle.
- The effects were specific to Tetraselmis chuii and not observed with a placebo.

## Abstract

Superoxide dismutase-rich Tetraselmis chuii (T. chuii) is derived from marine microalgae and has been reported to increase gene expression of nuclear factor erythroid 2-related factor 2 (NRF2) and related antioxidant enzymes in myoblast tissue culture models. Human research has indicated that T. chuii supplementation can improve recovery from exercise-induced muscle damage, but its effects on endurance exercise performance and the molecular bases that may underlie any ergogenic effects are unclear. Healthy participants underwent 14 days of supplementation with 25 mg·day−1
T. chuii and placebo in a randomized, double-blind, crossover experimental design. Prior to and following each supplementation period, participants completed a high-intensity cycling test to assess time to exhaustion and peak oxygen uptake (V˙O2peak). A resting skeletal muscle biopsy was collected after both supplementation periods to assess gene expression changes. Compared to pre-supplementation values, V˙O2peak was increased following T. chuii (p = 0.013) but not placebo (p = 0.66). Fold-change in glutathione peroxidase 7 [(GPX7) 1.26 ± 1.37], glutathione-disulfide reductase [(GSR) 1.22 ± 1.41], glutathione S-transferase Mu 3 [(GSTM3) 1.34 ± 1.49], peroxiredoxin 6 [(PRDX6) 1.36 ± 1.57], extracellular signal-regulated kinase 3 [(ERK3) 1.92 ± 2.42], NRF2 (1.62 ± 2.16), p38 alpha [(p38a) 1.33 ± 1.58] and sirtuin 1 [(SIRT1) 1.73 ± 2.25] gene expression were higher after T. chuii compared to placebo supplementation (p < 0.05). Short-term T. chuii supplementation increased V˙O2peak and skeletal muscle gene expression of key enzymatic antioxidants (GPX7, GSR, GSTM3, and PRDX6), signalling kinases (ERK3 and p38a), post-translational regulators (SIRT1), and transcription factors (NRF2) that may protect against cellular stress insults.

## Linked entities

- **Genes:** GABPA (GA binding protein transcription factor subunit alpha) [NCBI Gene 2551], GPX7 (glutathione peroxidase 7) [NCBI Gene 2882], GSR (glutathione-disulfide reductase) [NCBI Gene 2936], GSTM3 (glutathione S-transferase mu 3) [NCBI Gene 2947], PRDX6 (peroxiredoxin 6) [NCBI Gene 9588], MAPK6 (mitogen-activated protein kinase 6) [NCBI Gene 5597], p38a (p38a MAP kinase) [NCBI Gene 42866], SIRT1 (sirtuin 1) [NCBI Gene 23411]

## Full-text entities

- **Genes:** GPX7 (glutathione peroxidase 7) [NCBI Gene 2882] {aka CL683, GPX6, GPx-7, GSHPx-7, NPGPx}, MAPK14 (mitogen-activated protein kinase 14) [NCBI Gene 1432] {aka CSBP, CSBP1, CSBP2, CSPB1, EXIP, Mxi2}, GSTM3 (glutathione S-transferase mu 3) [NCBI Gene 2947] {aka GST5, GSTB, GSTM3-3, GSTM3TV2, GTM3, hGSTM3-3}, SIRT1 (sirtuin 1) [NCBI Gene 23411] {aka SIR2, SIR2L1, SIR2alpha}, MAPK6 (mitogen-activated protein kinase 6) [NCBI Gene 5597] {aka ERK3, HsT17250, PRKM6, p97MAPK}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, PRDX6 (peroxiredoxin 6) [NCBI Gene 9588] {aka 1-Cys, AOP2, HEL-S-128m, LPCAT-5, NSGPx, PRX}, GSR (glutathione-disulfide reductase) [NCBI Gene 2936] {aka CNSHA10, GR, GSRD, HEL-75, HEL-S-122m}
- **Diseases:** muscle damage (MESH:D009133)
- **Species:** Tetraselmis chui (species) [taxon 63592], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12024062/full.md

## References

58 references — full list in the complete paper: https://tomesphere.com/paper/PMC12024062/full.md

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Source: https://tomesphere.com/paper/PMC12024062