Chen Guang-Di, Tanaka Chiemi, Henderson Donald
Center for Hearing and Deafness, SUNY at Buffalo, Buffalo, NY 14214, USA.
Hear Res. 2008 Sep;243(1-2):28-34. doi: 10.1016/j.heares.2008.05.008. Epub 2008 May 28.
The relationship between outer hair cell (OHC) loss and cochlear sensitivity is still unclear, because in many animal models there exist surviving but dysfunctional OHCs and also injured/dead inner hair cells (IHC). Styrene is an ototoxic agent, which targets and destroys OHCs starting from the third row to the second and first rows depending on the exposure level. The remaining cells may be less affected. In this experiment, rats were exposed to styrene by gavage at different doses (200-800 mg/kg/day) for varying periods (5 days/week for 3-12 weeks). An interesting finding was that the cochlear sensitivity was not affected in a few rats with all OHCs in the third row being destroyed by styrene. A further loss of OHCs was usually accompanied with a linear input/output (I/O) function of cochlear compound action potentials (CAP), indicating the loss of cochlear amplification. However, normal CAP amplitudes at the highest stimulation level of 90 dB SPL were often observed when all OHCs were destroyed, indicating normal function of the remaining IHCs. The OHC-loss/hearing-loss relation appeared to be a sigmoid-type function. Initially, styrene-induced OHC losses (<33%) did not result in a significant threshold shift. Then CAP threshold shift increased dramatically with OHC loss from 33% to 66%. Then, CAP threshold changed less with OHC loss. The data suggest a tri-modal relationship between OHC loss and cochlear amplification. That is, under the condition that all surviving OHCs are ideally functioning, the cochlear amplifier is not affected until 33% of OHCs are absent, then the gain of the amplifier decreases proportionally with the OHC loss, and at last the amplifier may fail completely when more than 67% of OHCs are lost.
外毛细胞(OHC)损失与耳蜗敏感性之间的关系仍不清楚,因为在许多动物模型中,存在存活但功能失调的OHC,以及受损/死亡的内毛细胞(IHC)。苯乙烯是一种耳毒性剂,根据暴露水平,它会从第三排开始,依次靶向并破坏OHC,直至第二排和第一排。其余细胞可能受影响较小。在本实验中,大鼠通过灌胃接受不同剂量(200 - 800毫克/千克/天)的苯乙烯暴露,持续不同时间(每周5天,共3 - 12周)。一个有趣的发现是,在一些第三排所有OHC都被苯乙烯破坏的大鼠中,耳蜗敏感性并未受到影响。OHC的进一步损失通常伴随着耳蜗复合动作电位(CAP)的线性输入/输出(I/O)功能变化,这表明耳蜗放大功能丧失。然而,当所有OHC都被破坏时,在90分贝声压级的最高刺激水平下,常常能观察到正常的CAP振幅,这表明剩余IHC功能正常。OHC损失与听力损失的关系似乎呈S形函数。最初,苯乙烯诱导的OHC损失(<33%)并未导致明显的阈值变化。然后,随着OHC损失从33%增加到66%,CAP阈值变化急剧增加。之后,随着OHC损失,CAP阈值变化较小。数据表明OHC损失与耳蜗放大之间存在三模态关系。也就是说,在所有存活的OHC都理想运作的情况下,直到33%的OHC缺失,耳蜗放大器才会受到影响,然后放大器的增益会随着OHC损失成比例下降,最后当超过67%的OHC丢失时,放大器可能会完全失效。