# Naturido alleviates amyloid β1–42-induced adverse effects in a transgenic Caenorhabditis elegans model of Alzheimer’s disease

**Authors:** Piyamas Sillapakong, Tokumitsu Wakabayashi, Koichi Suzuki, David M. Ojcius, David M. Ojcius, David M. Ojcius

PMC · DOI: 10.1371/journal.pone.0320636 · PLOS One · 2025-03-26

## TL;DR

Naturido, a cyclic peptide from a medicinal fungus, reduces Alzheimer’s-related toxicity in a worm model by improving learning, movement, and other Aβ1-42-induced issues.

## Contribution

Demonstrates Naturido’s ability to alleviate Aβ1-42-induced adverse effects in a transgenic C. elegans model of Alzheimer’s disease.

## Key findings

- Naturido improved associative learning impaired by Aβ1-42 in transgenic C. elegans.
- Naturido reduced serotonin hypersensitivity and locomotion deficits caused by Aβ1-42 overexpression.
- The findings suggest Naturido may be a candidate for Alzheimer’s prevention or treatment.

## Abstract

Alzheimer’s disease (AD) is a progressive neurodegenerative disorder primarily associated with aging. While the amyloid hypothesis is not the only explanation for AD pathogenesis, it is widely recognized that the accumulation of amyloid β (Aβ) protein triggers pathological changes in the brains of patients. In a previous study, we showed that Naturido, a cyclic peptide derived from the medicinal fungus (Isaria japonica) grown on domestic silkworms (Bombyx mori), could reverse several age-related deficits in senescence-accelerated mice. In this study, we explored the potential of Naturido to reduce Aβ-related toxicity in transgenic Caenorhabditis elegans models of AD, where human Aβ1-42 protein is overexpressed in neurons. Our results demonstrated that Naturido administration alleviated various phenotypes, including Aβ-induced impairment in associative learning, serotonin hypersensitivity, and locomotion in the transgenic C. elegans. These findings suggest the potential of Naturido as a candidate molecule for the prevention and/or treatment of AD.

## Linked entities

- **Proteins:** FDI57_gp42 (endonuclease)
- **Diseases:** Alzheimer’s disease (MONDO:0004975)
- **Species:** Caenorhabditis elegans (taxon 6239), Bombyx mori (taxon 7091), Isaria japonica (taxon 72233)

## Full-text entities

- **Diseases:** amyloid (MESH:C000718787), neurodegenerative disorder (MESH:D019636), AD (MESH:D000544), toxicity (MESH:D064420)
- **Chemicals:** serotonin (MESH:D012701), Naturido (-)
- **Species:** Caenorhabditis elegans (species) [taxon 6239], Mus musculus (house mouse, species) [taxon 10090], C. elegans [taxon 328850], Bombyx mori (domestic silkworm, species) [taxon 7091], Homo sapiens (human, species) [taxon 9606], Isaria japonica (species) [taxon 72233]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC11940425/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11940425/full.md

## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC11940425/full.md

---
Source: https://tomesphere.com/paper/PMC11940425