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Resistance of skin fibroblasts to peroxide and UV damage predicts hearing loss in aging mice.皮肤成纤维细胞对过氧化物和紫外线损伤的抵抗力预测衰老小鼠的听力损失。
Aging Cell. 2011 Apr;10(2):362-3. doi: 10.1111/j.1474-9726.2010.00668.x. Epub 2011 Feb 1.
2
Phenotype and genetics of progressive sensorineural hearing loss (Snhl1) in the LXS set of recombinant inbred strains of mice.LXS 系重组近交系小鼠进行性感觉神经性听力损失 (Snhl1) 的表型和遗传学研究。
PLoS One. 2010 Jul 7;5(7):e11459. doi: 10.1371/journal.pone.0011459.
3
Prevalence of noise-induced hearing loss in student musicians.学生音乐家噪声性听力损失的患病率。
Int J Audiol. 2010 Apr;49(4):309-16. doi: 10.3109/14992020903470809.
4
Epidemiology of hearing impairment and noise-induced hearing injury among U.S. military personnel, 2003-2005.美国军人听力损伤和噪声性听力损伤的流行病学,2003-2005 年。
Am J Prev Med. 2010 Jan;38(1 Suppl):S71-7. doi: 10.1016/j.amepre.2009.10.025.
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Age-related hearing loss: ear and brain mechanisms.年龄相关性听力损失:耳朵与大脑机制
Ann N Y Acad Sci. 2009 Jul;1170:708-17. doi: 10.1111/j.1749-6632.2009.03931.x.
6
Rapamycin fed late in life extends lifespan in genetically heterogeneous mice.在生命后期喂食雷帕霉素可延长基因异质小鼠的寿命。
Nature. 2009 Jul 16;460(7253):392-5. doi: 10.1038/nature08221. Epub 2009 Jul 8.
7
Genome-wide screening for genetic loci associated with noise-induced hearing loss.全基因组筛查与噪声性听力损失相关的基因位点。
Mamm Genome. 2009 Apr;20(4):207-13. doi: 10.1007/s00335-009-9178-5. Epub 2009 Apr 1.
8
Mechanisms and genes in human strial presbycusis from animal models.基于动物模型的人类耳蜗衰老性聋的机制与基因
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9
Inheritance patterns of progressive hearing loss in laboratory strains of mice.小鼠实验室品系中进行性听力损失的遗传模式。
Brain Res. 2009 Jun 24;1277:42-51. doi: 10.1016/j.brainres.2009.02.012. Epub 2009 Feb 21.
10
Aging outer hair cells (OHCs) in the Fischer 344 rat cochlea: function and morphology.费希尔344大鼠耳蜗中衰老的外毛细胞:功能与形态
Hear Res. 2009 Feb;248(1-2):39-47. doi: 10.1016/j.heares.2008.11.010. Epub 2008 Dec 10.

调节遗传异质性小鼠老年听力的等位基因。

Alleles that modulate late life hearing in genetically heterogeneous mice.

机构信息

Kresge Hearing Research Institute, Department of Otolaryngology, University of Michigan Medical School, Ann Arbor, MI, USA.

出版信息

Neurobiol Aging. 2012 Aug;33(8):1842.e15-29. doi: 10.1016/j.neurobiolaging.2011.12.034. Epub 2012 Feb 2.

DOI:10.1016/j.neurobiolaging.2011.12.034
PMID:22305187
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3346888/
Abstract

A genetically heterogeneous population of mice was tested for hearing at 8, 18, and 22 months by auditory brainstem response (ABR), and genotyped at 128 markers to identify loci that modulate late life hearing loss. Half of the test mice were exposed to noise for 2 hours at age 20 months. Polymorphisms affecting hearing at 18 months were noted on chromosomes 2, 3, 7, 10, and 15. Most of these loci had effects only on responses to 48 kHz stimuli, but a subset also influenced the auditory brainstem response at lower frequencies. Loci on chromosomes 4, 10, 12, and 14 had significant effects on hearing at 22 months in noise-exposed mice, and loci on chromosomes 10 and 11 had effects on mice not exposed to noise. Outer hair cell loss was modulated by polymorphisms on chromosomes 10, 11, 12, 17, and 19. Resistance to age-related hearing loss is thus modulated by a set of genetic effects, some age-specific, some frequency specific, some dependent on prior exposure to noise, and some of which compromise survival of cochlear hair cells.

摘要

一组遗传异质性的小鼠群体在 8、18 和 22 个月时通过听觉脑干反应(ABR)进行听力测试,并在 128 个标记处进行基因分型,以确定调节晚年听力损失的基因座。一半的测试小鼠在 20 个月大时暴露于 2 小时的噪声中。在 18 个月时影响听力的多态性出现在染色体 2、3、7、10 和 15 上。这些基因座中的大多数仅对 48 kHz 刺激的反应有影响,但一部分也影响低频的听觉脑干反应。在暴露于噪声的小鼠中,染色体 4、10、12 和 14 上的基因座对 22 个月时的听力有显著影响,而染色体 10 和 11 上的基因座对未暴露于噪声的小鼠有影响。外毛细胞的丧失受染色体 10、11、12、17 和 19 上的多态性调节。因此,年龄相关性听力损失的抗性受一组遗传效应调节,一些是年龄特异性的,一些是频率特异性的,一些取决于先前暴露于噪声,一些则影响耳蜗毛细胞的存活。