Henry K R
Department of Psychology, University of California, Davis.
Acta Otolaryngol. 1992;112(4):599-603. doi: 10.3109/00016489209137447.
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 F1 hybrid offspring were examined for noise-induced elevation of the auditory brainstem response (ABR) threshold. The F1 line had an intermediate degree of loss and the most uniform high frequency cochlear loss. Methylprednisolone was found to protect the F1 from noise-induced losses, whereas naloxone did not.
近交系小鼠作为人类噪声性听力损失的模型有几个优点。然而,近交系的同基因性质与人类情况非常不同,这可能使该物种作为听觉模型的价值降低。本实验从两种具有终生正常耳蜗功能的小鼠基因型开始:CBA/CaJ和AUS/sJ近交系。检测了这些品系及其F1杂交后代噪声诱发的听觉脑干反应(ABR)阈值升高情况。F1代有中度听力损失,且高频耳蜗损失最为一致。发现甲基强的松龙可保护F1代免受噪声诱发的听力损失,而纳洛酮则不能。