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ToxSci Advance Access published online on May 21, 2007

Toxicological Sciences, doi:10.1093/toxsci/kfm109
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Published by Oxford University Press 2007.

Promotion of Noise-Induced Cochlear Injury by Toluene and Ethylbenzene in the Rat

Laurence D. Fechter1, Caroline Gearhart1, Sherry Fulton1, Jerry Campbell2, Jeffrey Fisher2, Kwangsam Na3, David Cocker3, Alisa Nelson-Miller1, Patrick Moon4 and Benoit Pouyatos1

1 Loma Linda VA Medical Center, Loma Linda CA 92357 2 The University of Georgia 3 CE-CERT, University of California, Riverside 4 Loma Linda University School of Medicine

Corresponding author: Laurence Fechter, Research Service (151), Loma Linda VA Medical Center, 11201 Benton Street, Loma Linda, CA 92357, Larry.fechter{at}med.va.gov

Received March 15, 2007; revision received April 27, 2007; accepted April 28, 2007


   Abstract

Ethylbenzene + toluene are known individually to have ototoxic potential at high exposure levels and with prolonged exposure times generally of 4-16 weeks. Both ethylbenzene + toluene are minor constituents of JP-8 jet fuel; this fuel has recently been determined to promote susceptibility to noise-induced hearing loss. Therefore, the current study evaluates the ototoxic potential of combined exposure to ethylbenzene + toluene exposure in a ratio calculated from the average found in three laboratories . Rats received ethylbenzene + toluene by inhalation and half of them were subjected simultaneously to an octave band of noise (OBN) of 93-95 dB. Another group received only the noise exposure which was designed to produce a small, but permanent auditory impairment while an unexposed control group was also included. In two separate experiments, exposures occurred either repeatedly on 5 successive days for one week or for 5 days on two successive weeks to 4000mg/m3 total hydrocarbons for 6 h based upon initial pilot studies. The concentration of toluene was 400 ppm and the concentration of ethylbenzene was 660 ppm. Impairments in auditory function were assessed using distortion product otoacoustic emissions (DPOAE) and compound action potential (CAP) testing. Following completion of these tests, the organs of Corti were dissected to permit evaluation of hair cell loss. The uptake and elimination of the solvents was assessed by harvesting key organs at two time points following ethylbenzene + toluene exposure from additional rats not used for auditory testing. Similarly, glutathione levels were measured in light of suggestions that oxidative stress might result from solvent-noise exposures. Ethylbenzene + toluene exposure by itself at 4000 mg/m3 for 6 h did not impair cochlear function or yield a loss of hair cells. However, when combined with a 93 dB OBNexposure combined solvent + noise did yield a loss in auditory function and a clear potentiation of outer hair cell (OHC) death that exceeded the loss produced by noise alone. No evidence was found for a loss in total glutathione in lung, liver or brain as a consequence of ethylbenzene + toluene exposure.

Key Words: ethylbenzene + toluene; jet fuel; auditory function; ototoxicity.


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