Altschuler R A, Dolan D F, Halsey K, Kanicki A, Deng N, Martin C, Eberle J, Kohrman D C, Miller R A, Schacht J
Kresge Hearing Research Institute, Dept. of Otolaryngology, University of Michigan, Ann Arbor, MI, USA; Dept. of Cell and Developmental Biology, University of Michigan, Ann Arbor, MI, USA.
Kresge Hearing Research Institute, Dept. of Otolaryngology, University of Michigan, Ann Arbor, MI, USA.
Neuroscience. 2015 Apr 30;292:22-33. doi: 10.1016/j.neuroscience.2015.01.068. Epub 2015 Feb 7.
This study compared the timing of appearance of three components of age-related hearing loss that determine the pattern and severity of presbycusis: the functional and structural pathologies of sensory cells and neurons and changes in gap detection (GD), the latter as an indicator of auditory temporal processing. Using UM-HET4 mice, genetically heterogeneous mice derived from four inbred strains, we studied the integrity of inner and outer hair cells by position along the cochlear spiral, inner hair cell-auditory nerve connections, spiral ganglion neurons (SGN), and determined auditory thresholds, as well as pre-pulse and gap inhibition of the acoustic startle reflex (ASR). Comparisons were made between mice of 5-7, 22-24 and 27-29 months of age. There was individual variability among mice in the onset and extent of age-related auditory pathology. At 22-24 months of age a moderate to large loss of outer hair cells was restricted to the apical third of the cochlea and threshold shifts in the auditory brain stem response were minimal. There was also a large and significant loss of inner hair cell-auditory nerve connections and a significant reduction in GD. The expression of Ntf3 in the cochlea was significantly reduced. At 27-29 months of age there was no further change in the mean number of synaptic connections per inner hair cell or in GD, but a moderate to large loss of outer hair cells was found across all cochlear turns as well as significantly increased ABR threshold shifts at 4, 12, 24 and 48 kHz. A statistical analysis of correlations on an individual animal basis revealed that neither the hair cell loss nor the ABR threshold shifts correlated with loss of GD or with the loss of connections, consistent with independent pathological mechanisms.
本研究比较了与年龄相关的听力损失的三个组成部分出现的时间,这三个组成部分决定了老年性聋的模式和严重程度:感觉细胞和神经元的功能及结构病变,以及间隙检测(GD)的变化,后者作为听觉时间处理的一个指标。使用UM-HET4小鼠,即源自四个近交系的遗传异质性小鼠,我们通过沿耳蜗螺旋的位置研究了内、外毛细胞的完整性、内毛细胞-听神经连接、螺旋神经节神经元(SGN),并测定了听觉阈值,以及声惊吓反射(ASR)的预脉冲和间隙抑制。对5-7个月、22-24个月和27-29个月龄的小鼠进行了比较。小鼠在与年龄相关的听觉病理的发生和程度上存在个体差异。在22-24个月龄时,外毛细胞的中度至大量损失局限于耳蜗的顶部三分之一,听觉脑干反应中的阈值变化最小。内毛细胞-听神经连接也有大量且显著的损失,GD显著降低。耳蜗中Ntf3的表达显著降低。在27-29个月龄时,每个内毛细胞的突触连接平均数或GD没有进一步变化,但在所有耳蜗转弯处都发现外毛细胞有中度至大量损失,并且在4、12、24和48kHz时ABR阈值变化显著增加。基于个体动物的相关性统计分析表明,毛细胞损失和ABR阈值变化均与GD损失或连接损失无关,这与独立的病理机制一致。