Le Calvez S, Guilhaume A, Romand R, Aran J M, Avan P
Laboratory of Neurobiology, University Blaise-Pascal, Ensemble Universitaire des Cézeaux, Aubière, France.
Hear Res. 1998 Jun;120(1-2):51-61. doi: 10.1016/s0378-5955(98)00051-3.
In our companion paper (Le Calvez et al., 1998), the levels of distortion product otoacoustic emissions (DPOAE) were collected in the ears of CD1 mice with progressive degeneration of cochlear outer hair cells (OHC). Their comparison to standard functional measurements such as auditory-evoked brainstem responses (ABR) showed that CD1 ears could be classified as normal or impaired in a frequency-specific manner using DPOAE levels. The present work reports how DPOAE phases and levels of young CD1 mice were affected by varying the frequency ratio of eliciting stimuli at frequencies f1 and f2. Normally hearing CBA/J mice served as controls. The rate of phase change of DPOAE when f1 was varied and f2 was fixed allowed the group delay of DPOAE to be derived. The changes of DPOAE levels during this procedure disclosed bandpass characteristics that several reports (Fahey and Allen, 1986; Brown and Gaskill, 1990) assumed to be the reflection of important features of cochlear micromechanics, possibly in relation to the coupling of OHCs to the tectorial membrane. Group delays became significantly shorter when ABR thresholds exceeded 40 dB elevation. The bandpass filter characteristics strikingly depended on auditory function so that the optimal ratio f2/f1 progressively shifted from 1.24 to 1.50 or more when hearing loss increased. A difference was also noted between CD1 ears whose ABR thresholds were not yet increased and control CBA/J (optimal ratio 1.20). Scanning electron microscopy disclosed a variety of often minor OHC lesions that were only roughly correlated with cochlear function. However, the presence of abnormalities in the reticular lamina associated with early changes of DPOAE fine structure as a function of f2/f1 supported the hypothesis of some involvement of micromechanical features in the bandpass filter characteristics of DPOAE. The sensitivity of their measurement in pathological situations is potentially interesting.
在我们的姊妹论文(勒卡尔韦兹等人,1998年)中,收集了耳蜗外毛细胞(OHC)进行性退化的CD1小鼠耳朵中的畸变产物耳声发射(DPOAE)水平。将其与标准功能测量(如听性脑干反应,ABR)进行比较表明,使用DPOAE水平可以按频率特异性方式将CD1小鼠的耳朵分类为正常或受损。本研究报告了通过改变频率f1和f2处诱发刺激的频率比,年轻CD1小鼠的DPOAE相位和水平如何受到影响。听力正常的CBA/J小鼠作为对照。当f1变化而f2固定时,DPOAE的相位变化率可用于推导DPOAE的群延迟。在此过程中DPOAE水平的变化揭示了带通特性,几份报告(费伊和艾伦,1986年;布朗和加斯基尔,1990年)认为这反映了耳蜗微机械的重要特征,可能与OHC与盖膜的耦合有关。当ABR阈值超过40 dB升高时,群延迟显著缩短。带通滤波器特性明显取决于听觉功能,因此当听力损失增加时,最佳频率比f2/f1逐渐从1.24变为1.50或更高。在ABR阈值尚未升高的CD1小鼠耳朵和对照CBA/J小鼠(最佳比率1.20)之间也发现了差异。扫描电子显微镜揭示了各种通常较小的OHC病变,这些病变仅与耳蜗功能大致相关。然而,与DPOAE精细结构随f2/f1的早期变化相关的网状板异常的存在支持了微机械特征在DPOAE带通滤波器特性中有所参与的假设。它们在病理情况下测量的敏感性可能很有趣。