Gap detection ability declines with central auditory neurodegeneration following age-related cochlear synaptopathy

IF 2.7 4区 医学 Q3 NEUROSCIENCES European Journal of Neuroscience Pub Date : 2024-09-05 DOI:10.1111/ejn.16534
Takaomi Kurioka, Kunio Mizutari
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Abstract

Age-related hearing impairment (ARHI) is commonly associated with decreased auditory temporal resolution caused by auditory neurodegeneration. Age-related deterioration in gap detection ability, resulting in poor temporal auditory processing, is often attributed to pathophysiological changes in both the peripheral and central auditory systems. This study aimed to investigate whether the gap detection ability declines in the early stages of ageing and to determine its usefulness in detecting peripheral and central auditory degeneration. The study used 1-month-old (1 M), 6-month-old (6 M) and 12-month-old (12 M) mice to examine changes in gap detection ability and associated auditory pathophysiology. Although hearing thresholds did not significantly differ between the groups, the amplitude of auditory brainstem response (ABR) wave I decreased significantly in an age-dependent manner, consistent with age-related cochlear synaptopathy. The relative ABR amplitude ratio of waves 2 and 5 to wave 1 was significantly increased in 12 M mice, indicating that the central auditory system had increased in relative neuroactivity. A significant increase in gap detection thresholds was observed in 12 M mice compared to 1 M mice. Although cochlear synaptopathy and central hyperactivity were positively correlated with gap detection thresholds, central hyperactivity strongly influenced gap detection ability. In the cochlear nucleus and auditory cortex, the inhibitory synaptic expression of GAD65 and the expression of parvalbumin were significantly decreased in 12 M mice, consistent with central hyperactivity. Evaluating gap detection performance may allow the identification of decreased auditory temporal resolution in the early stages of ARHI, which is strongly associated with auditory neurodegeneration.

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与年龄相关的耳蜗突触病变后,间隙检测能力会随着中枢听觉神经变性而下降。
老年性听力损伤(ARHI)通常与听觉神经变性导致的听觉时间分辨率下降有关。与年龄相关的间隙检测能力下降导致听觉处理的时间性变差,通常归因于外周和中枢听觉系统的病理生理变化。本研究旨在调查间隙检测能力是否会在衰老的早期阶段下降,并确定其在检测外周和中枢听觉退化方面的作用。研究使用 1 个月大(1 M)、6 个月大(6 M)和 12 个月大(12 M)的小鼠来检测间隙检测能力的变化以及相关的听觉病理生理学。虽然各组之间的听阈没有明显差异,但听性脑干反应(ABR)波 I 的振幅却以年龄依赖性的方式显著下降,这与年龄相关的耳蜗突触病是一致的。在 12 M 小鼠中,第 2 波和第 5 波与第 1 波的相对 ABR 振幅比明显增加,这表明中枢听觉系统的神经活性相对增加。与 1 M 小鼠相比,12 M 小鼠的间隙检测阈值明显增加。虽然耳蜗突触病变和中枢亢进与间隙检测阈值呈正相关,但中枢亢进对间隙检测能力有很大影响。在 12 M 小鼠的耳蜗核和听觉皮层中,GAD65 的抑制性突触表达和副发光素的表达均显著下降,这与中枢亢进一致。通过评估间隙检测性能,可以识别ARHI早期阶段听觉时间分辨率的降低,这与听觉神经变性密切相关。
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来源期刊
European Journal of Neuroscience
European Journal of Neuroscience 医学-神经科学
CiteScore
7.10
自引率
5.90%
发文量
305
审稿时长
3.5 months
期刊介绍: EJN is the journal of FENS and supports the international neuroscientific community by publishing original high quality research articles and reviews in all fields of neuroscience. In addition, to engage with issues that are of interest to the science community, we also publish Editorials, Meetings Reports and Neuro-Opinions on topics that are of current interest in the fields of neuroscience research and training in science. We have recently established a series of ‘Profiles of Women in Neuroscience’. Our goal is to provide a vehicle for publications that further the understanding of the structure and function of the nervous system in both health and disease and to provide a vehicle to engage the neuroscience community. As the official journal of FENS, profits from the journal are re-invested in the neuroscientific community through the activities of FENS.
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