Willott J F
Department of Psychology, Northern Illinois University, DeKalb 60115, USA.
J Am Acad Audiol. 1996 Jun;7(3):141-51.
Because hearing is accomplished by the brain (with neural input from the cochlea), presbyacusis can be ultimately accounted for by changes in brain activity that accompany aging. The anatomic and physiologic changes that accompany aging are of two basic types: the central effects of biological aging (CEBA) and the central effects of peripheral pathology (CEPP). Research using inbred mice and other animal models has provided insights into both CEPP and CEBA, and some implications of this research are reviewed, including the following. Age-related cochlear pathology results in changes in how frequency is "mapped" in the central auditory system (CAS), especially at higher anatomic levels, and this has potentially negative consequences for hearing. Aging and/or age-related hearing loss may impair neural inhibition in the CAS. CEPP may result in abnormalities in neural responses involved in binaural hearing and cause exaggerated "masking" of neural responses by noise. The extent of age-related anatomic change (CEBA and CEPP) varies among CAS subdivisions and accelerates during the terminal phase of life. Genes have been found to influence the time course and severity of presbyacusis as well as the role dietary restriction plays in ameliorating age-related hearing loss in mice.
由于听力是由大脑完成的(来自耳蜗的神经输入),老年性耳聋最终可归因于伴随衰老而来的大脑活动变化。伴随衰老出现的解剖学和生理学变化有两种基本类型:生物衰老的中枢效应(CEBA)和外周病理的中枢效应(CEPP)。使用近交系小鼠和其他动物模型的研究为CEPP和CEBA都提供了见解,本文将对该研究的一些启示进行综述,内容如下。与年龄相关的耳蜗病理会导致频率在中枢听觉系统(CAS)中“映射”方式的变化,尤其是在较高的解剖学水平,这对听力可能产生负面影响。衰老和/或与年龄相关的听力损失可能会损害CAS中的神经抑制。CEPP可能导致双耳听力中神经反应异常,并导致噪声对神经反应的过度“掩蔽”。与年龄相关的解剖学变化(CEBA和CEPP)程度在CAS各亚区有所不同,并在生命末期加速。已发现基因会影响老年性耳聋的时间进程和严重程度,以及饮食限制在改善小鼠与年龄相关听力损失中所起的作用。