Department of Otorhinolaryngology-Head & Neck Surgery, College of Medicine, CHA University, Seongnam 13496, Korea.
Cells. 2022 Jul 22;11(15):2266. doi: 10.3390/cells11152266.
Several recent preclinical studies have reported that dynamic changes in miRNA expression contribute to hearing function. This study aims to investigate miRNA expression changes in the cochlear nuclei (CN) of rats following chronic noise exposure. Eight-week-old rats ( = 14) were exposed to noise for 4 weeks. The control rats ( = 14) were raised under identical conditions without noise. Two months after noise exposure, the auditory brainstem response (ABR) was examined, and the cochlea and CN were harvested. In the CN, the expression levels of arc, neurocan, and brevican were measured ( = 6 per group). Furthermore, the expression levels of miRNAs and their predicted target genes were measured in the CN ( = 8 per group). ABR thresholds were elevated after 4 weeks of noise exposure, which were maintained for 3 months. In CN, the protein expression of arc and brevican was higher in the noise-exposed group than in the control group (0.95 [standard deviation (SD) = 0.53] vs. 3.19 [SD = 1.00], < 0.001 for arc and 1.02 [SD = 0.10] vs. 1.66 [SD = 0.24], < 0.001 for brevican). The noise-exposed rats exhibited lower expression levels of miR-758-5p, miR-15b-5p, miR-212-3p, miR-199a-5p, and miR-134-3p than the control rats (all < 0.001). The AMPK signaling pathway was predicted to be regulated by these miRNAs. The predicted target genes AKT3, SIRT1, and PRKAA1 were highly expressed in noise-exposed rats. In CN of noise-exposed rats, the miRNAs of miR-758-5p, miR-15b-5p, miR-212-3p, miR-199a-5p, and miR-134-3p were reduced and related to AMPK signaling including AKT3 and SIRT1 expression. These modulation of signaling pathways could mediate the increased expression of brevican in the CN of noise-exposed rats.
几项最近的临床前研究报告称,miRNA 表达的动态变化有助于听力功能。本研究旨在探讨慢性噪声暴露后耳蜗核(CN)中 miRNA 表达的变化。将 8 周龄大鼠(n = 14)暴露于噪声中 4 周。对照组大鼠(n = 14)在相同条件下饲养而不接触噪声。噪声暴露 2 个月后,检测听觉脑干反应(ABR),并采集耳蜗和 CN。在 CN 中,测量 arc、neurocan 和 brevican 的表达水平(每组 n = 6)。此外,还测量了 CN 中 miRNA 及其预测靶基因的表达水平(每组 n = 8)。噪声暴露 4 周后 ABR 阈值升高,并持续 3 个月。CN 中,暴露组的 arc 和 brevican 蛋白表达高于对照组(arc:0.95 [标准差(SD)= 0.53] 比 3.19 [SD = 1.00], < 0.001;brevican:1.02 [SD = 0.10] 比 1.66 [SD = 0.24], < 0.001)。与对照组相比,噪声暴露大鼠 miR-758-5p、miR-15b-5p、miR-212-3p、miR-199a-5p 和 miR-134-3p 的表达水平较低(均 < 0.001)。AMPK 信号通路被预测受这些 miRNA 调节。预测的靶基因 AKT3、SIRT1 和 PRKAA1 在噪声暴露大鼠中高表达。在噪声暴露大鼠的 CN 中,miR-758-5p、miR-15b-5p、miR-212-3p、miR-199a-5p 和 miR-134-3p 的 miRNA 减少,并与包括 AKT3 和 SIRT1 表达在内的 AMPK 信号相关。这些信号通路的调节可能介导了噪声暴露大鼠 CN 中 brevican 的表达增加。