4.5 Article

Metabolomics of Lung Microdissections Reveals Region- and Sex-Specific Metabolic Effects of Acute Naphthalene Exposure in Mice

Journal

TOXICOLOGICAL SCIENCES
Volume 184, Issue 2, Pages 214-222

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/toxsci/kfab110

Keywords

metabolomics; lung; microdissection; polycyclic aromatic hydrocarbons

Categories

Funding

  1. National Institutes of Health [R01 ES020867, P30 ES023513, U2C ES030158, T32 ES007059]

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The study found that naphthalene has region-specific toxic effects on the lungs of mice, causing cytotoxicity through cytochrome P450-mediated bioactivation. There are differences in metabolic responses and clearance rates of naphthalene between male and female mice, with females showing higher susceptibility. This research provides insights into potential mechanisms contributing to naphthalene toxicity and presents a novel approach for lung metabolomic analysis.
Naphthalene is a ubiquitous environmental contaminant produced by combustion of fossil fuels and is a primary constituent of both mainstream and side stream tobacco smoke. Naphthalene elicits region-specific toxicity in airway club cells through cytochrome P450 (P450)-mediated bioactivation, resulting in depletion of glutathione and subsequent cytotoxicity. Although effects of naphthalene in mice have been extensively studied, few experiments have characterized global metabolomic changes in the lung. In individual lung regions, we found metabolomic changes in microdissected mouse lung conducting airways and parenchyma obtained from animals sacrificed at 3 timepoints following naphthalene treatment. Data on 577 unique identified metabolites were acquired by accurate mass spectrometry-based assays focusing on lipidomics and nontargeted metabolomics of hydrophilic compounds. Statistical analyses revealed distinct metabolite profiles between the 2 lung regions. Additionally, the number and magnitude of statistically significant exposure-induced changes in metabolite abundance were different between airways and parenchyma for unsaturated lysophosphatidylcholines, dipeptides, purines, pyrimidines, and amino acids. Importantly, temporal changes were found to be highly distinct for male and female mice with males exhibiting predominant treatment-specific changes only at 2 h postexposure. In females, metabolomic changes persisted until 6 h postnaphthalene treatment, which may explain the previously characterized higher susceptibility of female mice to naphthalene toxicity. In both males and females, treatment-specific changes corresponding to lung remodeling, oxidative stress response, and DNA damage were observed. Overall, this study provides insights into potential mechanisms contributing to naphthalene toxicity and presents a novel approach for lung metabolomic analysis that distinguishes responses of major lung regions.

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