Elevated glutathione in researchers exposed to engineered nanoparticles due to potential adaptation to oxidative stress

Nanomedicine (Lond). 2024 Feb;19(3):185-198. doi: 10.2217/nnm-2023-0207. Epub 2024 Jan 26.

Abstract

Aim: To find a practical biomonitoring method for researchers exposed to nanoparticles causing oxidative stress. Methods: In a continuation of a study in 2016-2018, biological samples (plasma, urine and exhaled breath condensate [EBC]) were collected in 2019-2020 from 43 researchers (13.8 ± 3.0 years of exposure) and 45 controls. Antioxidant status was assessed using glutathione (GSH) and ferric-reducing antioxidant power, while oxidative stress was measured as thiobarbituric acid reactive substances, all using spectrophotometric methods. Researchers' personal nanoparticle exposure was monitored. Results: Plasma GSH was elevated in researchers both before and after exposure (p < 0.01); postexposure plasma GSH correlated with nanoparticle exposure, and GSH in EBC increased. Conclusion: The results suggest adaptation to chronic exposure to nanoparticles, as monitored by plasma and EBC GSH.

Keywords: adaptation; antioxidant status; inhalation; nanoparticles; occupational; oxidative stress.

Plain language summary

What is this study about? Identifying markers of oxidative stress and/or adaptation to oxidation stress could offer tools for monitoring exposure to nanoparticles in exposed researchers. In this study, we question whether these markers correlate with their personal exposure during the shift. What were the results? We found that exposure to nanoparticles correlated with the antioxidant marker glutathione, which is higher in workers who are already pre-exposed. What do the results mean? This study suggests that the researchers have adapted to nanoparticle exposure and are ready to combat oxidative stress. However, the similarity with increased markers of oxidative stress from asbestos and silica exposure, including nucleic acid oxidation, previously found in these researchers highlights the need for further research in this area to better understand and prevent potential future effects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antioxidants*
  • Biomarkers / metabolism
  • Breath Tests / methods
  • Glutathione
  • Nanoparticles*
  • Oxidative Stress
  • Thiobarbituric Acid Reactive Substances

Substances

  • Antioxidants
  • Glutathione
  • Thiobarbituric Acid Reactive Substances
  • Biomarkers