Integrative multiomics analysis of metabolic dysregulation induced by occupational benzene exposure in mice
Sydney ScofieldiD, Lisa KoshkoiD, Lukas StilgenbaueriD, Alix BoomsiD, Roxanne BérubéiD, Christopher Dennis KassotisiD, Chung-Ho LiniD, Hyejeong JangiD, Seongho KimiD, Paul M. StemmeriD, Adelheid M. LempradliD, Marianna SadagurskiiD
Abstract
Background: Type 2 Diabetes Mellitus (T2DM) is a significant public health burden. Emerging evidence links volatile organic compounds (VOCs), such as benzene to endocrine disruption and metabolic dysfunction. However, the effects of chronic environmentally relevant VOC exposures on metabolic health are still emerging. Objective: Building on our previous findings that benzene exposure at smoking levels (50 ppm) induces metabolic impairments in male mice, we investigated the effects of occupationally relevant, below OSHA approved, benzene exposure on metabolic health. Methods: Adult male C57BL/6 mice were exposed to 0.9ppm benzene 8 hours a day for 9 weeks. We assessed measures of metabolic homeostasis and conducted RNA and proteome sequencing on insulin-sensitive organs (liver, skeletal muscle, adipose tissue). Results: This low-dose exposure caused significant metabolic disruptions, including hyperglycemia, hyperinsulinemia, and insulin resistance. Transcriptomic analysis of liver, skeletal muscle, and adipose tissue identified key changes in metabolic and immune pathways especially in liver. Proteomic analysis of the liver revealed mitochondrial dysfunction as a shared feature, with disruptions in oxidative phosphorylation, mitophagy, and immune activation. Comparative analysis with high-dose (50 ppm) exposure showed both conserved and dose-specific transcriptomic changes in liver, particularly in metabolic and immune responses. Conclusions: Our study is the first to comprehensively assess the impacts of occupational benzene exposure on metabolic health, highlighting mitochondrial dysfunction as a central mechanism and the dose-dependent molecular pathways in insulin-sensitive organs driving benzene-induced metabolic imbalance. Our data indicate that current OSHA occupational exposure limits for benzene are insufficient, as they could result in adverse metabolic health in exposed workers, particularly men, following chronic exposure.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 14
- FWCI
- 2.30
- Field percentile
- top 12%
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Microglial NF-κB Signaling Deficiency Protects Against Metabolic Disruptions Caused by Volatile Organic Compound via Modulating the Hypothalamic Transcriptome
Lucas Kniess Debarba, Hashan S. M. Jayarathne, … Marianna Sadagurski·bioRxiv·Nov 8, 2023
- Metabolic Reprogramming by In Utero Maternal Benzene Exposure
L. Koshko, L. K. Debarba, … M. Sadagurski·bioRxiv·Oct 12, 2020
- Acarbose Protects From Central and Peripheral Metabolic Imbalance Induced by Benzene Exposure
L. K. Debarba, A. Mulka, … M. Sadagurski·bioRxiv·Mar 19, 2020
- Prenatal benzene exposure alters offspring hypothalamic development predisposing to metabolic disease in later life
Lisa Koshko, Sydney Scofield, … Marianna Sadagurski·bioRxiv·Jan 5, 2023
- Long-term metabolic consequences of acute dioxin exposure differ between male and female mice
M. P. Hoyeck, H. Blair, … J. E. Bruin·bioRxiv·Sep 9, 2019
- Female mice exposed to low-doses of dioxin during pregnancy and lactation have increased susceptibility to diet-induced obesity and diabetes
M. P. Hoyeck, R. C. Merhi, … J. E. Bruin·bioRxiv·Jul 9, 2020