Acute toluene exposure and rat visual function in proportion to momentary brain concentration
William K Boyes1, Mark Bercegeay, Quentin Todd Krantz
1Neurotoxicology Division, U.S. Environmental Protection Agency, Research Triangle Park, North Carolina 27711, USA. boyes.william@epa.gov
Summary
Acute toluene exposure significantly impacts neurophysiological function, specifically visual evoked potentials (VEP). Brain toluene concentration directly correlates with VEP amplitude deficits, indicating a clear dose-response relationship.
Area of Science:
- Neuroscience
- Toxicology
- Pharmacokinetics
Background:
- Toluene is an industrial solvent with known neurotoxic effects.
- Understanding the relationship between toluene exposure and neurophysiological changes is crucial for occupational safety.
Purpose of the Study:
- To determine the relationship between brain toluene concentration and neurophysiological function after acute exposure.
- To assess the dose-response relationship between toluene and visual evoked potentials (VEP).
Main Methods:
- Two experiments involving adult male Long-Evans rats exposed to varying concentrations of toluene (1000-4000 ppm).
- Physiologically based pharmacokinetic modeling to estimate brain toluene concentration.
- Measurement of neurophysiological function using pattern-elicited visual evoked potentials (VEP).
Main Results:
- Toluene exposure reduced the response amplitude of the major spectral component of the VEP (F2).
- A significant relationship was found between estimated brain toluene concentration and VEP amplitude deficits.
- 3000 ppm toluene caused similar VEP deficits during and after exposure, while 4000 ppm showed partial adaptation post-exposure.
Conclusions:
- Acute toluene exposure causes neurophysiological deficits that are directly related to the estimated concentration of toluene in the brain.
- VEP amplitude reduction serves as a sensitive indicator of acute toluene neurotoxicity.
- The findings highlight the importance of monitoring brain toluene levels to understand neurotoxic effects.


