Abstract
Inbred strains of mice have several advantages as models for human noise-induced hearing loss. However, the isogenic nature of inbred lines is very unlike the human condition, and may make this species less valuable as an auditory model. The present experiments start with two mouse genotypes having lifelong normal cochlear functions: The CBA/CaJ and the AUS/sJ inbred strains. These strains and their F, hybrid offspring were examined for noise-induced elevation of the auditory brainstem response (ABR) threshold. The F, line had an intermediate degree of loss and the most uniform high frequency cochlear loss. Methylprednisolone was found to protect the F] from noise-induced losses, whereas naloxone did not.