Department of Otolaryngology, University of Ulsan College of Medicine, Asan Medical Center, Seoul 138-736, Republic of Korea.
Department of Otolaryngology (Head and Neck Surgery), Konkuk University Hospital, Seoul 143-729, Republic of Korea.
Environ Toxicol Pharmacol. 2013 Sep;36(2):463-471. doi: 10.1016/j.etap.2013.05.012. Epub 2013 Jun 3.
All-trans retinoic acid (ATRA) is reported to reduce hair cell loss and hearing deterioration caused by noise-induced hearing loss (NIHL). The present study investigates the involvement of peroxiredoxin 6 (Prdx 6) in ATRA-mediated protection of temporary threshold shift of hearing. Mice fed with ATRA before or after exposure to white noise showed a faster recovery than untreated controls within 1 week, with a concomitant increase of cochlear Prdx 6 expression. Treatment of mouse auditory cells with ATRA induced Prdx 6 expression. A putative retinoic acid (RA)-response element (RARE) was identified in a murine Prdx 6 promoter region. Prdx 6 promoter activities were elevated in wild-type reporter plasmid-transfected cells, whereas no significant change in activity was in those with RARE-disrupted mutant reporter. RA receptor α (RARα) functions as a transactivator of Prdx 6 gene expression. These findings suggest that ATRA-induced Prdx 6 expression may be associated with rapid recovery from temporary NIHL.
全反式视黄酸(ATRA)可减少噪声性听力损失(NIHL)引起的毛细胞损失和听力恶化。本研究探讨了过氧化物酶 6(Prdx 6)在 ATRA 介导的听力暂时阈移保护中的作用。在暴露于白噪声之前或之后用 ATRA 喂养的小鼠在 1 周内比未处理的对照组恢复得更快,同时耳蜗 Prdx 6 表达增加。用 ATRA 处理小鼠听觉细胞诱导 Prdx 6 表达。在鼠 Prdx 6 启动子区域中鉴定出一个假定的视黄酸(RA)反应元件(RARE)。野生型报告质粒转染细胞中的 Prdx 6 启动子活性升高,而 RARE 破坏突变报告中的活性没有明显变化。RA 受体 α(RARα)作为 Prdx 6 基因表达的转录激活因子。这些发现表明,ATRA 诱导的 Prdx 6 表达可能与暂时性 NIHL 的快速恢复有关。