Coppens A G, Kiss R, Heizmann C W, Deltenre P, Poncelet L
Department of Anatomy and Embryology, Laboratory of Veterinary Anatomy, Free University of Brussels, Faculty of Medicine, Belgium.
Hear Res. 2001 Nov;161(1-2):65-71. doi: 10.1016/s0378-5955(01)00354-9.
Histopathological investigation was conducted on both inner ears from a 4.5-month-old Rottweiler puppy with electrophysiologically confirmed bilateral deafness. The lesions were restricted to the organ of Corti and spiral ganglion that both displayed severe degenerative changes. The outer hair cells were less affected than the inner hair cells. The number of spiral ganglion neurons was reduced, and remaining neurons were altered. The basal and middle cochlear turns were more affected than the apical one. The vestibules were normal. Immunostaining with calbindin, calretinin, S100A1 and S100A6 polyclonal antisera was helpful in identifying different cell-types in the degenerated cochlea. The early and severe spiral ganglion cell degeneration is an uncommon finding no matter the species. Such lesions bear significance within the frame of cochlear implants technology for deaf infants.
对一只4.5个月大、经电生理证实为双侧耳聋的罗威纳幼犬的双耳进行了组织病理学研究。病变局限于柯蒂氏器和螺旋神经节,二者均表现出严重的退行性变化。外毛细胞比内毛细胞受影响较小。螺旋神经节神经元数量减少,剩余神经元发生改变。耳蜗基部和中部比顶部受影响更严重。前庭正常。用钙结合蛋白、钙视网膜蛋白、S100A1和S100A6多克隆抗血清进行免疫染色有助于识别退化耳蜗中的不同细胞类型。无论物种如何,早期和严重的螺旋神经节细胞变性都是不常见的发现。此类病变在聋儿人工耳蜗植入技术框架内具有重要意义。