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长期短时长噪声刺激会加剧耳蜗中与年龄相关的炎症和氧化应激。

Age-Related Inflammation and Oxidative Stress in the Cochlea Are Exacerbated by Long-Term, Short-Duration Noise Stimulation.

作者信息

Fuentes-Santamaría Verónica, Alvarado Juan Carlos, Mellado Susana, Melgar-Rojas Pedro, Gabaldón-Ull María Cruz, Cabanes-Sanchis José J, Juiz José M

机构信息

Instituto de Investigación en Discapacidades Neurológicas (IDINE), Albacete, Spain.

Facultad de Medicina, Universidad de Castilla-La Mancha, Albacete, Spain.

出版信息

Front Aging Neurosci. 2022 Apr 5;14:853320. doi: 10.3389/fnagi.2022.853320. eCollection 2022.

Abstract

We have previously reported that young adult rats exposed to daily, short-duration noise for extended time periods, develop accelerated presbycusis starting at 6 months of age. Auditory aging is associated with progressive hearing loss, cell deterioration, dysregulation of the antioxidant defense system, and chronic inflammation, among others. To further characterize cellular and molecular mechanisms at the crossroads between noise and age-related hearing loss (ARHL), 3-month-old rats were exposed to a noise-accelerated presbycusis (NAP) protocol and tested at 6 and 16 months of age, using auditory brainstem responses, Real-Time Reverse Transcription-Quantitative PCR (RT-qPCR) and immunocytochemistry. Chronic noise-exposure leading to permanent auditory threshold shifts in 6-month-old rats, resulted in impaired sodium/potassium activity, degenerative changes in the lateral wall and spiral ganglion, increased lipid peroxidation, and sustained cochlear inflammation with advancing age. Additionally, at 6 months, noise-exposed rats showed significant increases in the gene expression of antioxidant enzymes (superoxide dismutase 1/2, glutathione peroxidase 1, and catalase) and inflammation-associated molecules [ionized calcium binding adaptor molecule 1, interleukin-1 beta (IL-1β), and tumor necrosis factor-alpha]. The levels of IL-1β were upregulated in the spiral ganglion and spiral ligament, particularly in type IV fibrocytes; these cells showed decreased levels of connective tissue growth factor and increased levels of 4-hydroxynonenal. These data provide functional, structural and molecular evidence that age-noise interaction contributes to exacerbating presbycusis in young rats by leading to progressive dysfunction and early degeneration of cochlear cells and structures. These findings contribute to a better understanding of NAP etiopathogenesis, which is essential as it affects the life quality of young adults worldwide.

摘要

我们之前曾报道,成年幼鼠若长时间每日暴露于短时长噪声环境中,会在6个月大时开始出现加速的老年性聋。听觉衰老与渐进性听力损失、细胞退化、抗氧化防御系统失调以及慢性炎症等有关。为了进一步阐明噪声与年龄相关性听力损失(ARHL)之间交叉点的细胞和分子机制,对3个月大的大鼠采用噪声加速老年性聋(NAP)方案进行处理,并在6个月和16个月大时使用听觉脑干反应、实时逆转录定量PCR(RT-qPCR)和免疫细胞化学进行检测。慢性噪声暴露导致6个月大的大鼠出现永久性听觉阈值偏移,致使钠/钾活性受损、外侧壁和螺旋神经节发生退行性变化、脂质过氧化增加以及随着年龄增长耳蜗炎症持续存在。此外,在6个月时,噪声暴露大鼠的抗氧化酶(超氧化物歧化酶1/2、谷胱甘肽过氧化物酶1和过氧化氢酶)和炎症相关分子[离子化钙结合衔接分子1、白细胞介素-1β(IL-1β)和肿瘤坏死因子-α]的基因表达显著增加。IL-1β水平在螺旋神经节和螺旋韧带中上调,尤其是在IV型纤维细胞中;这些细胞的结缔组织生长因子水平降低,4-羟基壬烯醛水平升高。这些数据提供了功能、结构和分子证据,表明年龄与噪声的相互作用通过导致耳蜗细胞和结构的渐进性功能障碍和早期退化,促使幼鼠的老年性聋加剧。这些发现有助于更好地理解NAP的发病机制,这至关重要,因为它影响着全球年轻人的生活质量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31e9/9016828/be7791b0e8cc/fnagi-14-853320-g001.jpg

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