# Nutraceutical Effects of Gastrodiae elata and Coenzyme Q10 on Oxidative Stress and Inflammatory Pathways in an In Vitro Gut–Prostate Axis Model

**Authors:** Rebecca Galla, Simone Mulè, Francesca Parini, Francesca Uberti

PMC · DOI: 10.3390/nu18050804 · Nutrients · 2026-02-28

## TL;DR

This study explores how a nutraceutical mix of Gastrodiae elata and coenzyme Q10 may help prostate health by reducing oxidative stress and inflammation in a lab model.

## Contribution

The novel contribution is demonstrating the combined effects of Gastrodiae elata and coenzyme Q10 on oxidative stress and inflammatory pathways in a gut–prostate in vitro model.

## Key findings

- The nutraceutical combination showed no cytotoxicity and high intestinal permeability.
- The formulation reduced oxidative stress and inflammatory markers like NF-κB, TNF-α, and IL-1β in prostate cells.
- It modulated androgen pathways by lowering 5-α-reductase activity and DHT levels while supporting testosterone balance.

## Abstract

Background/Objectives: Benign prostatic hyperplasia (BPH) is a multifactorial condition associated with androgen imbalance, oxidative stress, and chronic inflammation, leading to growing interest in food-derived bioactive compounds with multitarget activity. This study aimed to investigate the biological effects of a nutraceutical combination of Gastrodiae elata Blume extract and coenzyme Q10 (Q10), focusing on mechanisms relevant to prostate physiological balance using food-relevant in vitro models. Methods: An intestinal epithelial barrier model (Caco-2) was employed to assess intestinal tolerance and permeability of the tested compounds. Subsequently, a prostate epithelial–stromal co-culture exposed to dihydrotestosterone (DHT) was used to reproduce BPH-like cellular conditions. Oxidative stress, inflammatory mediators, androgen-related pathways, and markers of proliferation and apoptosis were evaluated following simulated intestinal passage. Results: The combined formulation showed no cytotoxic effects and demonstrated efficient intestinal permeability. After intestinal passage, the combination significantly reduced oxidative stress and inflammatory responses in the prostate co-culture, decreasing reactive oxygen species and pro-inflammatory mediators, including NF-κB, TNF-α, and IL-1β. In parallel, the formulation modulated androgen-related pathways by reducing 5-α-reductase activity and DHT levels while supporting testosterone homeostasis. Across some of the evaluated endpoints, the combined formulation tended to show more pronounced protective effects compared with the individual components. Conclusions: These results suggest that a combination of Gastrodiae elata and coenzyme Q10 may have a positive effect on prostate health. In the nutraceutical field, this food-based formulation could help support prostate health, probably through antioxidant, anti-inflammatory, and hormonal control mechanisms. Further studies using advanced experimental models are warranted.

## Linked entities

- **Proteins:** NFKB1 (nuclear factor kappa B subunit 1)
- **Chemicals:** coenzyme Q10 (PubChem CID 5281915), dihydrotestosterone (PubChem CID 10635)
- **Diseases:** Benign prostatic hyperplasia (MONDO:0010811)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}
- **Diseases:** Inflammatory (MESH:D007249), cytotoxic (MESH:D064420), BPH (MESH:D011470)
- **Chemicals:** reactive oxygen species (MESH:D017382), testosterone (MESH:D013739), Coenzyme Q10 (MESH:C024989), DHT (MESH:D013196)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12987350/full.md

## References

81 references — full list in the complete paper: https://tomesphere.com/paper/PMC12987350/full.md

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Source: https://tomesphere.com/paper/PMC12987350