# Volatile Organic Compounds in Cellular Headspace after Hyperbaric Oxygen Exposure: An In Vitro Pilot Study

**Authors:** Feiko J. M. de Jong, Thijs A. Lilien, Dominic W. Fenn, Thijs T. Wingelaar, Pieter-Jan A. M. van Ooij, Anke H. Maitland-van der Zee, Markus W. Hollmann, Rob A. van Hulst, Paul Brinkman

PMC · DOI: 10.3390/metabo14050281 · Metabolites · 2024-05-13

## TL;DR

This study explores how exposure to high oxygen levels affects volatile organic compounds in human lung cells, potentially linking them to oxygen toxicity.

## Contribution

The study introduces an in vitro model to investigate VOCs as potential biomarkers for pulmonary oxygen toxicity.

## Key findings

- Nonane, octanal, and decane showed significant differences between oxygen-exposed and control groups.
- VOC signal intensities were lower in the oxygen-exposed group despite increased cellular stress markers.
- The model shows promise for future research on POT biomarkers.

## Abstract

Volatile organic compounds (VOCs) might be associated with pulmonary oxygen toxicity (POT). This pilot study aims to identify VOCs linked to oxidative stress employing an in vitro model of alveolar basal epithelial cells exposed to hyperbaric and hyperoxic conditions. In addition, the feasibility of this in vitro model for POT biomarker research was evaluated. The hyperbaric exposure protocol, similar to the U.S. Navy Treatment Table 6, was conducted on human alveolar basal epithelial cells, and the headspace VOCs were analyzed using gas chromatography–mass spectrometry. Three compounds (nonane [p = 0.005], octanal [p = 0.009], and decane [p = 0.018]), of which nonane and decane were also identified in a previous in vivo study with similar hyperbaric exposure, varied significantly between the intervention group which was exposed to 100% oxygen and the control group which was exposed to compressed air. VOC signal intensities were lower in the intervention group, but cellular stress markers (IL8 and LDH) confirmed increased stress and injury in the intervention group. Despite the observed reductions in compound expression, the model holds promise for POT biomarker exploration, emphasizing the need for further investigation into the complex relationship between VOCs and oxidative stress.

## Linked entities

- **Chemicals:** nonane (PubChem CID 8141), octanal (PubChem CID 454), decane (PubChem CID 15600)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}
- **Diseases:** POT (MESH:D000860)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11123173/full.md

## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC11123173/full.md

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Source: https://tomesphere.com/paper/PMC11123173