Zenner H P, Ernst A
Department of Otolaryngology, University of Tübingen, Germany.
Prog Brain Res. 1993;97:21-30. doi: 10.1016/s0079-6123(08)62259-1.
In inner and outer hair cells, a sound event results mechano-electrically in a receptor potential from the hair cells by the functioning of apical and lateral K(+)-channels. However, after this point, the signal transfer is divided. Inner hair cells (IHC) release an unknown afferent transmitter. By contrast, outer hair cells (OHC) are proposed to produce mechanical ac and dc responses. In our model, the ac components of the sound signal, the carrier frequencies, determine the response of the OHC. Usually, they respond by ac and dc movements. The rapid ac movements of OHC, for which the underlying mechanism is unknown, may respond cycle-by-cycle to and interfere with the carrier frequency of the traveling wave. Near hearing threshold, they could drastically amplify the traveling wave thus contributing to the postulated cochlear amplifier. Active dc movements of the cytoskeleton of the cell body, as well as of the cuticular plate with the sensory hairs, are proposed to respond to millisecond changes of the sound stimulus over time. Such changes could be a modulation of the amplitude (AM), i.e., an increase or decrease of the sound pressure level (SPL), which is reflected in the envelope of the traveling wave. The active mechanical dc response of OHC to the amplitude (AM) and frequency modulation (FM) pattern is then expected to result in dc position changes of the reticular lamina (RL). These should control the operation point of the stereocilia, thus influencing their transfer function and sensitivity. In addition, experimental data suggest that there are modulations of the compliance of the organ of Corti (OC) and changes of its geometry. This dc modulation of micromechanical properties and geometry of the OC by active force generation of OHCs might contribute to automatic gain control, adaptation, TTS, as well as to the homeostasis of the basilar membrane location. In particular, the motile mechanism may protect the vulnerable cochlear partition against high sound pressure levels. Moreover, according to this model, changes of the sound signal with time are expected to be encoded in the actively produced dc movements of the RL. As the signal changes may carry important information (e.g., complex sound signal modulations such as formant transitions in speech), this is extracted and mechanically encoded by the proposed active dc mechanism. It cannot be excluded that the information-carrying dc signal is transferred to inner hair cells contributing to their adequate stimulus.(ABSTRACT TRUNCATED AT 400 WORDS)
在内外毛细胞中,声音事件通过顶端和侧向钾离子通道的作用,以机械电方式使毛细胞产生感受器电位。然而,在此之后,信号传递出现分化。内毛细胞(IHC)释放一种未知的传入递质。相比之下,外毛细胞(OHC)被认为会产生机械性交流和直流反应。在我们的模型中,声音信号的交流成分,即载波频率,决定了外毛细胞的反应。通常,它们通过交流和直流运动做出反应。外毛细胞快速的交流运动,其潜在机制尚不清楚,可能逐周期地对行波的载波频率做出反应并产生干扰。在接近听力阈值时,它们可能会大幅放大行波,从而对假定的耳蜗放大器做出贡献。细胞体以及带有感觉毛的角质板的细胞骨架的主动直流运动,被认为是对声音刺激随时间变化毫秒级的反应。这种变化可能是幅度调制(AM),即声压级(SPL)的增加或降低,这在行波的包络中有所体现。然后预计外毛细胞对幅度(AM)和频率调制(FM)模式的主动机械直流反应会导致网状板(RL)的直流位置变化。这些变化应该控制静纤毛的工作点,从而影响它们的传递函数和灵敏度。此外,实验数据表明,柯蒂氏器(OC)的顺应性存在调制以及其几何形状发生变化。外毛细胞通过主动产生力对OC的微机械特性和几何形状进行这种直流调制,可能有助于自动增益控制、适应、暂时性阈移(TTS)以及基底膜位置的稳态。特别是,运动机制可能保护脆弱的耳蜗隔板免受高声压级的影响。此外,根据这个模型,声音信号随时间的变化预计会被编码在RL主动产生的直流运动中。由于信号变化可能携带重要信息(例如,复杂的声音信号调制,如语音中的共振峰转换),这些信息会被所提出的主动直流机制提取并进行机械编码。不能排除携带信息的直流信号会传递到内毛细胞并对其适当刺激做出贡献的可能性。(摘要截断于400字)