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老年普通狨猴和恒河猴的超高频率神经性 presbycusis。

Neural presbycusis at ultra-high frequency in aged common marmosets and rhesus monkeys.

机构信息

Department of Otolaryngology-Head and Neck Surgery, Shanghai Ninth People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200011, P.R. China.

Ear Institute, Shanghai Jiaotong University School of Medicine, Shanghai 200011, P.R. China.

出版信息

Aging (Albany NY). 2021 Apr 27;13(9):12587-12606. doi: 10.18632/aging.202936.

DOI:10.18632/aging.202936
PMID:33909598
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8148503/
Abstract

The aging of the population and environmental noise have contributed to high rates of presbycusis, also known as age-related hearing loss (ARHL). Because mice have a relatively short life span, murine models have not been suitable for determining the mechanism of presbycusis development and methods of diagnosis. Although the common marmoset, a non-human primate (NHP), is an ideal animal model for studying age-related diseases, its auditory spectrum has not been systematically studied. Auditory brainstem responses (ABRs) from 38 marmosets of different ages demonstrated that auditory function correlated with age. Hearing loss in geriatric common marmosets started at ultra-high frequency (>16 kHz), then extended to lower frequencies. Despite age-related deterioration of ABR threshold and amplitude in marmosets, outer hair cell (OHC) function remained stable at all ages. Spiral ganglion neurons (SGNs), which are the first auditory neurons in the auditory system, were found to degenerate distinctly in aged common marmosets, indicating that neural degeneration caused presbycusis in these animals. Similarly, age-associated ABR deterioration without loss of OHC function was observed in another NHP, rhesus monkeys. Audiometry results from these two species of NHP suggested that NHPs were ideal for studying ARHL and that neural presbycusis at high frequency may be prevalent in primates.

摘要

人口老龄化和环境噪声导致了较高的老年性聋(presbycusis)发病率,又称与年龄相关的听力损失(ARHL)。由于小鼠的寿命相对较短,因此它们并不是研究老年性聋发病机制和诊断方法的理想模型。尽管作为非人类灵长类动物(NHP)的普通狨猴是研究与年龄相关疾病的理想动物模型,但它们的听觉频谱尚未得到系统研究。对不同年龄普通狨猴的听觉脑干反应(ABR)进行分析表明,听觉功能与年龄相关。老年普通狨猴的听力损失始于超高频(>16 kHz),然后扩展到较低频率。尽管普通狨猴的 ABR 阈值和振幅随年龄增长而逐渐恶化,但外毛细胞(OHC)功能在所有年龄段均保持稳定。作为听觉系统中的第一级听觉神经元,螺旋神经节神经元(SGN)在老年普通狨猴中明显退化,这表明在这些动物中,神经退化导致了老年性聋。同样,在另一种 NHP——恒河猴中也观察到了与 OHC 功能丧失无关的年龄相关性 ABR 恶化。这两种 NHP 的听力测试结果表明,NHP 非常适合研究 ARHL,高频的神经性老年性聋可能在灵长类动物中较为普遍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a168/8148503/8cf413c67783/aging-13-202936-g006.jpg
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Hear Res. 2020 Sep 1;394:107999. doi: 10.1016/j.heares.2020.107999. Epub 2020 Jun 18.
2
The common marmoset as suitable nonhuman alternative for the analysis of primate cochlear development.普通狨猴可作为分析灵长类耳蜗发育的合适非人类替代品。
FEBS J. 2021 Jan;288(1):325-353. doi: 10.1111/febs.15341. Epub 2020 May 15.
3
Adeno-associated virus vector enables safe and efficient Cas9 activation in neonatal and adult Cas9 knockin murine cochleae.
普通狨猴耳蜗中钠钾ATP酶的细胞特异性α和β亚基表达模式。
Sci Rep. 2025 Jul 23;15(1):26814. doi: 10.1038/s41598-025-12239-5.
4
Single-cell profiling identifies hair cell SLC35F1 deficiency as a signature of primate cochlear aging.单细胞分析确定毛细胞SLC35F1缺陷是灵长类动物耳蜗衰老的一个特征。
Nat Aging. 2025 Jun 20. doi: 10.1038/s43587-025-00896-0.
5
Conditional Overexpression of Neuritin in Supporting Cell Protects Cochlear Hair Cell and Delays Age-Related Hearing Loss by Enhancing Autophagy.支持细胞中神经突蛋白的条件性过表达通过增强自噬保护耳蜗毛细胞并延缓年龄相关性听力损失。
Int J Mol Sci. 2025 Apr 14;26(8):3709. doi: 10.3390/ijms26083709.
6
Age-related hearing loss in older adults: etiology and rehabilitation strategies.老年人与年龄相关的听力损失:病因及康复策略
Front Neurosci. 2024 Oct 1;18:1428564. doi: 10.3389/fnins.2024.1428564. eCollection 2024.
7
Sheep as a large animal model for hearing research: comparison to common laboratory animals and humans.绵羊作为听力研究的大型动物模型:与常见实验动物及人类的比较。
Lab Anim Res. 2023 Nov 27;39(1):31. doi: 10.1186/s42826-023-00182-3.
8
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Sci Rep. 2022 Nov 17;12(1):19811. doi: 10.1038/s41598-022-24380-6.
腺相关病毒载体可在新生和成年 Cas9 基因敲入小鼠耳蜗中实现安全有效的 Cas9 激活。
Gene Ther. 2020 Aug;27(7-8):392-405. doi: 10.1038/s41434-020-0124-1. Epub 2020 Jan 31.
4
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Stem Cell Res Ther. 2019 Dec 2;10(1):365. doi: 10.1186/s13287-019-1437-0.
5
The nuclear transcription factor FoxG1 affects the sensitivity of mimetic aging hair cells to inflammation by regulating autophagy pathways.核转录因子 FoxG1 通过调节自噬途径影响模拟衰老毛细胞对炎症的敏感性。
Redox Biol. 2020 Jan;28:101364. doi: 10.1016/j.redox.2019.101364. Epub 2019 Oct 29.
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7
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9
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10
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Clin Geriatr Med. 2018 May;34(2):163-174. doi: 10.1016/j.cger.2018.01.001. Epub 2018 Feb 14.