Suppr超能文献

尿石素 A 通过诱导自噬来预防 C57BL/6J 小鼠的年龄相关性听力损失。

Urolithin A prevents age-related hearing loss in C57BL/6J mice likely by inducing mitophagy.

机构信息

Department of Otolaryngology-Head and Neck Surgery, Chosun University College of Medicine, Gwangju, Republic of Korea.

Department of Otolaryngology-Head and Neck Surgery, Chosun University College of Medicine, Gwangju, Republic of Korea; Department of Biomedical Sciences, Graduate School of Chosun University, Gwangju, Republic of Korea.

出版信息

Exp Gerontol. 2024 Nov;197:112589. doi: 10.1016/j.exger.2024.112589. Epub 2024 Sep 24.

Abstract

Mitochondrial dysfunction with aging is associated with the development of age-related hearing loss. Mitophagy is a cardinal mechanism to maintain a healthy mitochondrial population through the turnover of damaged mitochondria. Declining mitophagy with age causes a buildup of damaged mitochondria, leading to sensory organ dysfunction. The effect of Urolithin A (UA), a mitophagy inducer, was investigated on age-related hearing loss in a mouse model. C57BL/6J mice were treated with UA from 6 to 10 months of age. UA attenuated an auditory brainstem responses (ABR) threshold shift at 8, 16, and 32 kHz frequencies, and improved mitochondrial DNA integrity and ATP production in the cochlea and auditory cortex. The mRNA levels of mitophagy-related genes and protein levels of PINK1, Parkin, BNIP3, and LC3B increased in the cochlea and auditory cortex. The expression of mitophagosomes and mitophagolysosomes in the cochlea, spiral ganglion, auditory cortex, and inferior colliculus increased, together with the expression of Parkin and BNIP3 in the cochlea, spiral ganglion, auditory cortex, and inferior colliculus. These results indicate that UA counteracted mitophagy decline in the auditory system and prevented age-related hearing loss. UA can be used as a potential agent to prevent age-related hearing loss.

摘要

衰老导致的线粒体功能障碍与年龄相关性听力损失的发展有关。自噬是通过清除受损线粒体来维持健康线粒体群体的主要机制。随着年龄的增长,自噬的下降会导致受损线粒体的积累,从而导致感觉器官功能障碍。自噬诱导剂尿石素 A (UA) 对小鼠模型中年龄相关性听力损失的影响进行了研究。C57BL/6J 小鼠从 6 到 10 个月大时接受 UA 治疗。UA 可减轻 8、16 和 32 kHz 频率的听觉脑干反应 (ABR) 阈值变化,并改善耳蜗和听觉皮层中的线粒体 DNA 完整性和 ATP 产生。耳蜗和听觉皮层中与自噬相关的基因的 mRNA 水平和 PINK1、Parkin、BNIP3 和 LC3B 的蛋白水平增加。耳蜗、螺旋神经节、听觉皮层和下丘中的自噬体和自噬溶酶体表达增加,同时耳蜗、螺旋神经节、听觉皮层和下丘中的 Parkin 和 BNIP3 表达也增加。这些结果表明,UA 逆转了听觉系统中的自噬下降,并预防了年龄相关性听力损失。UA 可作为预防年龄相关性听力损失的潜在药物。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验