Circadian rhythm disruptions exacerbate inner ear damage in a murine endolymphatic hydrops model

昼夜节律 每2 内淋巴水肿 内耳 毛细胞 耳蜗 内科学 内分泌学 生物 神经科学 医学 时钟 生物钟 梅尼埃病 疾病
作者
B. Y. Pang,Yijiang Bai,Yongjia Chen,Shuai Zhang,Zhenhang Xu,Chenglong Li,Ze-Qun Nie,Heng Liu,Zihang Guo,Jie Ling,Lingyun Mei
出处
期刊:The FASEB Journal [Wiley]
卷期号:39 (1): e70310-e70310
标识
DOI:10.1096/fj.202402445r
摘要

Abstract Meniere's disease (MD) is an inner ear disease characterized by endolymphatic hydrops (EH). Maintaining a regular daily routine is crucial for MD patients. However, the relationship between circadian rhythms and MD remains unclear. Therefore, we investigated the effect of circadian rhythm on endolymphatic hydrops and its underlying mechanisms. Mice with endolymphatic hydrops were subjected to chronic jet lag (CJL) conditions to simulate the MD patients under circadian rhythm disruptions. We assessed whether this disruption would exacerbate inner ear damage with endolymphatic hydrops. RNA‐seq of the inner ear and bioinformatic analysis were performed. Then, the expression of PER2, AQP2, AQP4, AQP5, and BDNF were assessed, and the morphological changes were evaluated in the inner ear. Our findings showed circadian rhythm disruption affected the cochlear internal clock genes in the inner ear, particularly in mice with EH. EH mice under CJL conditions exhibited exacerbated hearing impairment and an increased severity of EH. GO enrichment analysis revealed that the regulation of fluid homeostasis and neurotransmitter release at synapses were significantly enriched. Disruption of circadian rhythms disturbed the expression pattern of PER2, reduced BDNF levels, and affected the expression of aquaporins in the cochlea. Moreover, the disruption of circadian rhythm compromised inner hair cell synapses and auditory nerve fibers. This study indicated that disruption of circadian rhythms may exacerbate inner ear damage in endolymphatic hydrops mice by affecting the aquaporins and compromising synapses and auditory nerves in the inner ear. BDNF and PER2 may play a central role in these pathophysiological processes.
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