Archie's Cochlear Implant Laboratory, The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario, Canada.
Brain Topogr. 2011 Oct;24(3-4):204-19. doi: 10.1007/s10548-011-0181-2. Epub 2011 Apr 11.
In the present paper, we review what is currently known about the effects of deafness on the developing human auditory system and ask: Without use, does the immature auditory system lose the ability to normally function and mature? Any change to the structure or function of the auditory pathways resulting from a lack of activity will have important implications for future use through an auditory prosthesis such as a cochlear implant. Data to date show that deafness in children arrests and disrupts normal auditory development. Multiple changes to the auditory pathways occur during the period of deafness with the extent and type of change being dependent upon the age and stage of auditory development at onset of deafness, the cause or type of deafness, and the length of time the immature auditory pathways are left without significant input. Structural changes to the auditory nerve, brainstem, and cortex have been described in animal models of deafness as well in humans who are deaf. Functional changes in deaf auditory pathways have been evaluated by using a cochlear implant to stimulate the auditory nerve with electrical pulses. Studies of electrically evoked activity in the immature deaf auditory system have demonstrated that auditory brainstem development is arrested and that thalamo-cortical areas are vulnerable to being taken over by other competitive inputs (cross-modal plasticity). Indeed, enhanced peripheral sight and detection of visual movement in congenitally deaf cats and adults have been linked to activity in specific areas of what would normally be auditory cortex. Cochlear implants can stimulate developmental plasticity in the auditory brainstem even after many years of deafness in childhood but changes in the auditory cortex are limited, at least in part, by the degree of reorganization which occurred during the period of deafness. Consequently, we must identify hearing loss rapidly (i.e., at birth for congenital deficits) and provide cochlear implants to appropriate candidates as soon as possible. Doing so has facilitated auditory development in the thalamo-cortex and allowed children who are deaf to perceive and use spoken language.
在本文中,我们回顾了目前已知的耳聋对人类听觉系统发育的影响,并提出以下问题:在没有使用的情况下,未成熟的听觉系统是否会失去正常运作和成熟的能力?由于缺乏活动而导致听觉通路的结构或功能发生任何变化,都将对未来通过听觉假体(如人工耳蜗)的使用产生重要影响。迄今为止的数据表明,儿童耳聋会阻止并扰乱正常的听觉发育。在耳聋期间,听觉通路会发生多种变化,其变化的程度和类型取决于耳聋发生时的听觉发育年龄和阶段、耳聋的原因或类型以及未成熟听觉通路没有得到显著输入的时间长短。在耳聋的动物模型以及耳聋的人类中,已经描述了听觉神经、脑干和皮质的结构变化。通过使用人工耳蜗用电脉冲刺激听觉神经,评估了耳聋听觉通路的功能变化。对未成熟耳聋听觉系统的电诱发活动的研究表明,听觉脑干发育受阻,丘脑-皮质区容易被其他竞争输入(交叉模态可塑性)接管。事实上,在先天性耳聋的猫和成年人中,增强的外围视力和对视觉运动的检测与正常听觉皮层的特定区域的活动有关。即使在儿童期多年耳聋后,人工耳蜗也可以刺激听觉脑干的发育可塑性,但听觉皮层的变化是有限的,至少部分原因是耳聋期间发生的重组程度。因此,我们必须尽快(例如,对于先天性听力损失,应在出生时)识别出听力损失,并尽快为合适的候选人提供人工耳蜗。这样做促进了丘脑-皮质的听觉发育,并使耳聋的儿童能够感知和使用口语。