# Alleviating Effects of Ethanol Extract from Acremonium terricola Culture on Patulin Toxicity

**Authors:** Haiyan Lin, Savindi Kaushalya Edirisinghe, Ijeoma Esther Okolo, Zhen Chen, Juan Sun, Wei Hong, Ruiyu Zhu

PMC · DOI: 10.3390/antiox14050509 · Antioxidants · 2025-04-24

## TL;DR

A fungal extract helps reduce the harmful effects of patulin, a toxic compound, by boosting antioxidants in worms.

## Contribution

The study reveals the molecular mechanism and effectiveness of Acremonium terricola extract in mitigating patulin toxicity.

## Key findings

- EEAT treatment improved locomotion and antioxidant enzyme activities in patulin-exposed C. elegans.
- Key compounds like coumarin and trigonelline showed strong binding to targets SIR-2.1 and DAF-2.
- EEAT extract effectively reduces oxidative damage caused by patulin exposure.

## Abstract

Exposure to patulin (PAT) poses a significant health risk to animals, emphasizing the need for natural, safe substances to mitigate toxicity. Acremonium terricola culture (ATC), a fungal fermentation-derived feed additive, is known for its antioxidant properties, yet its potential to alleviate mycotoxin-induced toxicity remains largely uninvestigated. In this study, the ethanol extracts from the ATC (EEAT) were prepared with a total phenolic content of 67.9 mg GAE/g and a total flavonoid content of 32.7 mg RE/g. Ultra-high performance liquid chromatography coupled with tandem mass spectrometry (UPLC-ESI-MS/MS) analysis was employed to investigate the bioactive components in EEAT. In PAT-exposed Caenorhabditis elegans models, EEAT treatment significantly enhanced locomotory capacity and elevated antioxidant enzyme activities by 63.1% (SOD) and 90.1% (GSH-ST), respectively. Molecular docking analysis revealed that key active compounds in EEAT, such as coumarin, succinic acid, and trigonelline, exhibited effective binding affinities to potential targets SIR-2.1 and DAF-2. Notably, coumarin and trigonelline were most effective in alleviating PAT toxicity, as evidenced by rescued locomotor rates and oxidative impairment in C. elegans. Our findings not only elucidate the molecular basis of EEAT-mediated PAT mitigation but also establish A. terricola culture as a sustainable antioxidant.

## Linked entities

- **Chemicals:** patulin (PubChem CID 4696), coumarin (PubChem CID 323), succinic acid (PubChem CID 1110), trigonelline (PubChem CID 5570)
- **Species:** Caenorhabditis elegans (taxon 6239)

## Full-text entities

- **Genes:** daf-2 (Insulin-like receptor subunit beta;Protein kinase domain-containing protein;receptor protein-tyrosine kinase) [NCBI Gene 175410], sir-2.1 (NAD-dependent protein deacetylase sir-2.1) [NCBI Gene 177924]
- **Diseases:** Toxicity (MESH:D064420)
- **Chemicals:** Ethanol (MESH:D000431), GAE (-), PAT (MESH:D010365), trigonelline (MESH:C009560), succinic acid (MESH:D019802), flavonoid (MESH:D005419), coumarin (MESH:C030123)
- **Species:** Sarocladium terricola (species) [taxon 1610694], Caenorhabditis elegans (species) [taxon 6239], A. terricola [taxon 181075], C. elegans [taxon 328850]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12108246/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12108246/full.md

## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12108246/full.md

---
Source: https://tomesphere.com/paper/PMC12108246