# Neuroproteomic Profiling of the Anxiolytic Potential of Stypopodium zonale in Drosophila

**Authors:** Lymelsie Aponte Ramos, Xandra Pena Díaz, Ricardo M. Cruz Sánchez, Ana E. Rodríguez De Jesús, Yadira M. Cantres Rosario, Eduardo L. Tosado Rodríguez, Abiel Roche Lima, Loyda M. Meléndez, Ricardo Chiesa

PMC · DOI: 10.3390/ijms27052240 · International Journal of Molecular Sciences · 2026-02-27

## TL;DR

This study explores the anxiety-reducing effects of a tropical marine algae in fruit flies using a neuroproteomics approach.

## Contribution

It integrates natural product drug discovery with neuroproteomics in an invertebrate model system.

## Key findings

- 66 significantly differentially abundant proteins were identified in Drosophila after treatment with Stypopodium zonale extract.
- IPA analysis suggested inhibition of the Protein Kinase A (PKA) signaling pathway and interaction with Dop1R2 (DAMB).
- The study provides a foundation for isolating bioactive compounds from S. zonale for further behavioral validation.

## Abstract

Anxiety disorders are the most prevalent mental health conditions worldwide, yet current treatments remain suboptimal, with benzodiazepines carrying risks of tolerance and dependence. These limitations motivate the search for novel anxiolytics. Tropical marine macroalgae represent a promising source of neuroactive metabolites. Here, we investigate the anxiolytic potential of Stypopodium zonale using a neuroproteomics-based approach in Drosophila melanogaster. Crude organic extracts were prepared via ultrasonic-assisted extraction and administered acutely to adult flies for six hours. Proteins from fly heads were quantified and analyzed using liquid chromatography-tandem mass spectrometry (LC-MS/MS), revealing 66 significantly differentially abundant proteins (fold change ≥ |1.5|, p ≤ 0.05), 72.7% of which were less abundant in the extract-treated group. Principal component analysis demonstrated clear separation between control and experimental samples. Ingenuity Pathway Analysis (IPA) mapped 33 of the differentially abundant proteins to human orthologs and identified significant predicted inhibition of the Protein Kinase A (PKA) signaling pathway. An IPA Interaction Network enabled the construction of a preliminary working model, suggesting that the extract may antagonize Drosophila’s Dop1R2 (DAMB). Overall, this study integrates natural product drug discovery with neuroproteomics in an invertebrate model system, providing a foundation for future behavioral validation and isolation of bioactive compounds from S. zonale.

## Linked entities

- **Proteins:** Dop1R2 (Dopamine 1-like receptor 2), Dop1R2 (Dopamine 1-like receptor 2)
- **Species:** Drosophila melanogaster (taxon 7227)

## Full-text entities

- **Genes:** Dop1R2 (Dopamine 1-like receptor 2) [NCBI Gene 43484] {aka CG18741, CG7569, D1R2, D2R, DAMB, DDR2}, Pka-R1 (Protein kinase, cAMP-dependent, regulatory subunit type 1) [NCBI Gene 40305] {aka 18304, CG12452, CG18677, CG3263, CG42341, CdkR}
- **Diseases:** Anxiety disorders (MESH:D001008)
- **Chemicals:** benzodiazepines (MESH:D001569)
- **Species:** Drosophila melanogaster (fruit fly, species) [taxon 7227], Homo sapiens (human, species) [taxon 9606], Stypopodium zonale (species) [taxon 200428]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12984897/full.md

## References

56 references — full list in the complete paper: https://tomesphere.com/paper/PMC12984897/full.md

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Source: https://tomesphere.com/paper/PMC12984897