# Cutaneous effects of ovatoxin-a: an in vitro study on human skin keratinocytes

**Authors:** Alessandra D’Arelli, Michela Carlin, Silvio Sosa, Chiara Melchiorre, Fabio Varriale, Luciana Tartaglione, Michela Varra, David Kulis, Donald M. Anderson, Mark Poli, Aurelia Tubaro, Carmela Dell’Aversano, Marco Pelin

PMC · DOI: 10.1007/s00204-025-04229-3 · Archives of Toxicology · 2025-10-31

## TL;DR

This study examines how ovatoxin-a affects human skin cells, finding it less potent than palytoxin but sharing similar mechanisms of toxicity.

## Contribution

The study reveals that ovatoxin-a shares the same molecular target and ROS-dependent mechanism as palytoxin in skin cells.

## Key findings

- Ovatoxin-a reduced cell viability with lower potency than palytoxin in human keratinocytes.
- Ovatoxin-a and palytoxin share the same molecular target and ROS-dependent cytotoxicity mechanism.
- Exposure to ovatoxin-a caused similar ROS production as palytoxin after 1 hour.

## Abstract

Ovatoxin-a (OVTX-a) is the main palytoxin (PLTX) analogue produced by the marine benthic dinoflagellate Ostreopsis cf. ovata from the Mediterranean area, where it poses risks for human health mainly through inhalation of marine aerosols and/or skin contact with contaminated seawater. Herein, we highlight the effects of OVTX-a, in comparison to PLTX, at the skin level using human HaCaT keratinocytes, employing a sample containing OVTX-a at 86% purity. After 4 h exposure, OVTX-a reduced cell viability (EC50 = 8.3 × 10−9 M) with one order of magnitude lower potency than PLTX (EC50 = 3.7 × 10−10 M). Accordingly, OVTX-a induced lower levels of cell necrosis and mitochondrial depolarization than PLTX, but a 1-h-exposure to each toxin provoked similar increases in ROS production. Moreover, cells co-exposure to ouabain, an inhibitor of Na+/K+ ATPase, the molecular target of PLTX, or to diphenyliodonium chloride, a non-specific inhibitor of flavoprotein-based enzymes involved in PLTX-induced oxidative stress, suggested that OVTX-a and PLTX share not only the same molecular target, but also the same mechanism of ROS-dependent cytotoxicity. Overall, these results provide new evidence on OVTX-a hazard characterization at the skin level, clarifying its mechanism of action at the basis of cutaneous adverse effects experienced by bathers during O. cf. ovata blooms.

The online version contains supplementary material available at 10.1007/s00204-025-04229-3.

## Linked entities

- **Proteins:** nrv1 (nervana 1)
- **Chemicals:** ovatoxin-a (PubChem CID 90479618), palytoxin (PubChem CID 11105289), ouabain (PubChem CID 439501), diphenyliodonium chloride (PubChem CID 73870)
- **Species:** Ostreopsis cf. ovata (taxon 119758), Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** necrosis (MESH:D009336), cytotoxicity (MESH:D064420)
- **Chemicals:** PLTX (MESH:C010272), ROS (-), ouabain (MESH:D010042), diphenyliodonium chloride (MESH:C031291)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** HaCaT — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_0038)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12886334/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12886334/full.md

## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12886334/full.md

---
Source: https://tomesphere.com/paper/PMC12886334