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线粒体功能障碍和氧化应激在感音神经性听力损失中的作用。

Role of mitochondrial dysfunction and oxidative stress in sensorineural hearing loss.

机构信息

Department of Surgery (Otolaryngology), Yale University School of Medicine, New Haven, CT, 06510, USA; Department of Physiology, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, 1023, New Zealand.

Department of Surgery (Otolaryngology), Yale University School of Medicine, New Haven, CT, 06510, USA; Department of Otolaryngology - Head and Neck Surgery, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200125, China; Ear Institute, Shanghai Jiao Tong University School of Medicine, Shanghai, 200125, China.

出版信息

Hear Res. 2023 Jul;434:108783. doi: 10.1016/j.heares.2023.108783. Epub 2023 Apr 29.

Abstract

Sensorineural hearing loss (SNHL) can either be genetically inherited or acquired as a result of aging, noise exposure, or ototoxic drugs. Although the precise pathophysiological mechanisms underlying SNHL remain unclear, an overwhelming body of evidence implicates mitochondrial dysfunction and oxidative stress playing a central etiological role. With its high metabolic demands, the cochlea, particularly the sensory hair cells, stria vascularis, and spiral ganglion neurons, is vulnerable to the damaging effects of mitochondrial reactive oxygen species (ROS). Mitochondrial dysfunction and consequent oxidative stress in cochlear cells can be caused by inherited mitochondrial DNA (mtDNA) mutations (hereditary hearing loss and aminoglycoside-induced ototoxicity), accumulation of acquired mtDNA mutations with age (age-related hearing loss), mitochondrial overdrive and calcium dysregulation (noise-induced hearing loss and cisplatin-induced ototoxicity), or accumulation of ototoxic drugs within hair cell mitochondria (drug-induced hearing loss). In this review, we provide an overview of our current knowledge on the role of mitochondrial dysfunction and oxidative stress in the development of SNHL caused by genetic mutations, aging, exposure to excessive noise, and ototoxic drugs. We also explore the advancements in antioxidant therapies for the different forms of acquired SNHL that are being evaluated in preclinical and clinical studies.

摘要

感音神经性听力损失 (SNHL) 既可以是遗传的,也可以是由于衰老、噪声暴露或耳毒性药物引起的获得性的。尽管导致 SNHL 的精确病理生理机制尚不清楚,但大量证据表明线粒体功能障碍和氧化应激起着中心病因学作用。由于其高代谢需求,耳蜗,特别是感觉毛细胞、血管纹和螺旋神经节神经元,容易受到线粒体活性氧 (ROS) 的破坏性影响。耳蜗细胞中线粒体功能障碍和随之而来的氧化应激可能是由遗传性线粒体 DNA (mtDNA) 突变引起的(遗传性听力损失和氨基糖苷类诱导的耳毒性),随着年龄的增长积累获得性 mtDNA 突变(年龄相关性听力损失),线粒体过载和钙失调(噪声诱导的听力损失和顺铂诱导的耳毒性),或耳毒性药物在毛细胞线粒体中的积累(药物诱导的听力损失)。在这篇综述中,我们概述了我们目前对由遗传突变、衰老、过度暴露于噪声和耳毒性药物引起的 SNHL 中,线粒体功能障碍和氧化应激作用的了解。我们还探讨了不同形式的获得性 SNHL 的抗氧化治疗方法的进展,这些方法正在临床前和临床研究中进行评估。

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