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线粒体DNA 4834缺失对听力的影响。

The effect of the mtDNA4834 deletion on hearing.

作者信息

Kong Wei-Jia, Hu Yu-Juan, Wang Qiong, Wang Ying, Han Yue-Chen, Cheng Hua-Mao, Kong Wen, Guan Min-Xin

机构信息

Department of Otorhinolaryngology, Union Hospital of Tongji Medical College, Huazhong Science and Technology University, Jiefang Avenue 1277, Wuhan, China.

出版信息

Biochem Biophys Res Commun. 2006 May 26;344(1):425-30. doi: 10.1016/j.bbrc.2006.03.060. Epub 2006 Mar 24.

Abstract

Mutations in mitochondrial DNA (mtDNA) are associated with diverse pathological states in humans, notably sensorineural deafness. In humans, mtDNA4977 deletion, known as common deletion, is thought to play a critical role in presbyacusis. A similar mtDNA deletion occurs in the naturally aging rats is mtDNA4834 deletion. Today, it is still obscure about the effect of common mtDNA deletion on the presbyacusis and hearing loss. We establish a model of rat associated with mtDNA4834 deletion in inner ear by d-galactose. It was found that the malondialdehyde (MDA) increased with superoxide dismutase (SOD) decreasing in the inner ear of the rat treated with d-galactose than of the control. However, there was no significant difference in elevation of ABR threshold between the rat with mtDNA4834 deletion induced by d-galactose and control. After aminoglycoside antibiotic injected, the hearing threshold of the rats carrying mtDNA4834 deletion increased significantly compared with the rats without mtDNA4834 deletion. The results show that resembled accelerated aging in the inner ear of the rat could be induced by injecting d-galactose. Moreover, those suggest that mtDNA4834 deletion can not directly induce the hearing loss, but acting as a predisposing factor which can greatly enhance the sensitivity of the inner ear to the aminoglycoside antibiotic.

摘要

线粒体DNA(mtDNA)突变与人类多种病理状态相关,尤其是感音神经性耳聋。在人类中,mtDNA4977缺失,即所谓的常见缺失,被认为在老年性耳聋中起关键作用。在自然衰老的大鼠中发生的类似mtDNA缺失是mtDNA4834缺失。如今,常见mtDNA缺失对老年性耳聋和听力损失的影响仍不清楚。我们通过d-半乳糖建立了一种内耳与mtDNA4834缺失相关的大鼠模型。结果发现,与对照组相比,用d-半乳糖处理的大鼠内耳中丙二醛(MDA)增加,超氧化物歧化酶(SOD)减少。然而,d-半乳糖诱导的mtDNA4834缺失大鼠与对照组之间的听性脑干反应(ABR)阈值升高没有显著差异。注射氨基糖苷类抗生素后,携带mtDNA4834缺失的大鼠的听力阈值与未携带mtDNA4834缺失的大鼠相比显著升高。结果表明,注射d-半乳糖可诱导大鼠内耳出现类似加速衰老的现象。此外,这些结果表明,mtDNA4834缺失不能直接诱导听力损失,但作为一个易感因素,可大大增强内耳对氨基糖苷类抗生素的敏感性。

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