Department of Otolaryngology, Northwestern University Feinberg School of Medicine, Chicago, United States of America.
Department of Biomedical Engineering, Northwestern University, Evanston, United States of America.
Sci Rep. 2018 Feb 14;8(1):3033. doi: 10.1038/s41598-018-21336-7.
Exposure to noise and ototoxic drugs are responsible for much of the debilitating hearing loss experienced by about 350 million people worldwide. Beyond hearing aids and cochlear implants, there have been no other FDA approved drug interventions established in the clinic that would either protect or reverse the effects of hearing loss. Using Auditory Brainstem Responses (ABR) in a guinea pig model, we demonstrate that fluvastatin, an inhibitor of HMG-CoA reductase, the rate-limiting enzyme of the mevalonate pathway, protects against loss of cochlear function initiated by high intensity noise. A novel synchrotron radiation based X-ray tomographic method that imaged soft tissues at micrometer resolution in unsectioned cochleae, allowed an efficient, qualitative evaluation of the three-dimensional internal structure of the intact organ. For quantitative measures, plastic embedded cochleae were sectioned followed by hair cell counting. Protection in noise-exposed cochleae is associated with retention of inner and outer hair cells. This study demonstrates the potential of HMG-CoA reductase inhibitors, already vetted in human medicine for other purposes, to protect against noise induced hearing loss.
暴露于噪声和耳毒性药物是导致全球约 3.5 亿人出现听力损伤的主要原因。除了助听器和人工耳蜗植入物外,临床上还没有其他经 FDA 批准的药物干预措施来保护或逆转听力损失的影响。我们使用豚鼠模型中的听觉脑干反应(ABR)证明,氟伐他汀是 HMG-CoA 还原酶的抑制剂,即甲羟戊酸途径的限速酶,可预防高强度噪声引发的耳蜗功能丧失。一种新的基于同步辐射的 X 射线断层摄影方法可以以微米分辨率对未经切片的耳蜗中的软组织进行成像,从而可以高效、定性地评估完整器官的三维内部结构。对于定量测量,将塑料包埋的耳蜗进行切片,然后进行毛细胞计数。在噪声暴露的耳蜗中观察到的保护作用与内毛细胞和外毛细胞的保留有关。这项研究表明,HMG-CoA 还原酶抑制剂具有潜力,这些抑制剂已经在人类医学中用于其他目的,可预防噪声引起的听力损失。