# Dose-Related Structural and Functional Modifications of Mitochondria Are Induced In Vitro by Low Ozone Concentrations

**Authors:** Chiara Rita Inguscio, Elisa Dalla Pozza, Ilaria Dando, Gabriele Tabaracci, Osvaldo Angelini, Pietro Maria Picotti, Manuela Malatesta, Barbara Cisterna

PMC · DOI: 10.3390/ijms27052267 · 2026-02-28

## TL;DR

Low ozone doses cause temporary changes in mitochondria structure and function, which may support their use in medical treatments.

## Contribution

The study reveals the dose-dependent effects of low ozone on mitochondrial structure and function in muscle cells.

## Key findings

- Low ozone doses increased mitochondrial area and cristae extension.
- Ozone enhanced electron transport chain complexes and antioxidant enzymes.
- Mitochondrial changes were temporary, disappearing after 48 hours.

## Abstract

In the last decades, ozone (O3)-based medical treatments have become a widely applied complementary therapy for several pathological conditions. O3 is administered at low dosages since the induction of a mild oxidative stress does not cause damage but stimulates the antioxidant cell response through the nuclear factor erythroid 2-related factor 2 (Nrf2). Mitochondria are sensitive to even mild oxidative stress, thus being a responsive target for O3. This study aimed to evaluate the mitochondrial response to low O3 doses used for medical treatments. As the skeletal muscle represents a primary target in local O3 treatments, a murine non-tumoral muscle cell line was selected as an appropriate in vitro model. Transmission electron microscopy, biochemistry, and flow cytometry provided original information on the O3 dose-dependent modifications of mitochondrial structural and molecular features. Low O3 doses promoted an increase in mitochondrial area and in cristae extension, as well as an enhancement of the electron transport chain complexes and of antioxidant catalase and manganese-dependent superoxide dismutase. Nrf2 maintained its association with the outer mitochondrial membrane, thus exerting its protective role. All mitochondrial modifications were observed 24 h after treatment and disappeared after 48 h, demonstrating that cells promptly respond to the O3-driven oxidative stress, effectively restoring homeostasis.

## Linked entities

- **Genes:** GABPA (GA binding protein transcription factor subunit alpha) [NCBI Gene 2551]
- **Proteins:** Cat (Catalase)
- **Chemicals:** ozone (PubChem CID 24823), O3 (PubChem CID 24823)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Nfe2l2 (nuclear factor, erythroid derived 2, like 2) [NCBI Gene 18024] {aka Nrf2}, Cat (catalase) [NCBI Gene 12359] {aka 2210418N07, Cas-1, Cas1, Cs-1}
- **Chemicals:** O3 (MESH:D010126)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12986512/full.md

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Source: https://tomesphere.com/paper/PMC12986512