Sun Yu, Yu Jintao, Lin Xi, Tang Wenxue
Department of Otolaryngology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, PR China.
Department of Otolaryngology, Emory University School of Medicine, 615 Michael Street, Atlanta, GA 30322-3030, USA.
Sci Rep. 2016 Mar 3;6:22573. doi: 10.1038/srep22573.
Noise-induced hearing loss (NIHL) is an important occupational disorder. However, the molecular mechanisms underlying NIHL have not been fully clarified; therefore, the condition lacks effective therapeutic methods. Cyclooxygenase-2 (Cox-2) is an inducible enzyme involved in the synthesis of prostaglandins, and has been implicated in many pathophysiological events, such as oxidative stress and inflammation. In this study, we investigated the possible role of Cox-2 in the mechanisms of NIHL and the therapeutic effect of the Cox-2 inhibitor NS398 on NIHL using a mouse model. We demonstrated that Cox-2 is constitutively expressed in the mouse cochlea, and its expression could be dramatically up-regulated by high levels of noise exposure. Furthermore, we demonstrated that pre-treatment with the Cox-2 inhibitor NS398 could inhibit Cox-2 expression during noise overstimulation; and could attenuate noise-induced hearing loss and hair cell damage. Our results suggest that Cox-2 is involved in the pathogenesis of NIHL; and pharmacological inhibition of Cox-2 has considerable therapeutic potential in NIHL.
噪声性听力损失(NIHL)是一种重要的职业性疾病。然而,NIHL潜在的分子机制尚未完全阐明;因此,这种疾病缺乏有效的治疗方法。环氧化酶-2(Cox-2)是一种参与前列腺素合成的诱导酶,并且与许多病理生理事件有关,如氧化应激和炎症。在本研究中,我们使用小鼠模型研究了Cox-2在NIHL机制中的可能作用以及Cox-2抑制剂NS398对NIHL的治疗效果。我们证明Cox-2在小鼠耳蜗中组成性表达,并且其表达可被高强度噪声暴露显著上调。此外,我们证明用Cox-2抑制剂NS398预处理可在噪声过度刺激期间抑制Cox-2表达;并且可减轻噪声性听力损失和毛细胞损伤。我们的结果表明Cox-2参与NIHL的发病机制;并且对Cox-2的药理学抑制在NIHL中具有相当大的治疗潜力。