Morest D K, Kim J, Bohne B A
Department of Anatomy, School of Medicine, University of Connecticut Health Center, Farmington, USA.
Hear Res. 1997 Jan;103(1-2):151-68. doi: 10.1016/s0378-5955(96)00172-4.
Terminal axonal degeneration in the brain following cochlear lesions was studied with the Nauta-Rasmussen method. Losses of hair cells and myelinated cochlear fibers were assessed. The cochleotopic map projected, from apex to base, on the ventral-to-dorsal axes of the cochlear nuclei. The cochleotopic correspondence was better for loss of cochlear nerve fibers and inner hair cells, than for outer hair cells. Cochlear fibers were traced to all parts of the cochlear nucleus, including the small-cell shell, also to cell-group Y and the flocculus. Terminal axonal degeneration in nuclei of the superior olivary complex, lateral lemniscus, and inferior colliculus was interpreted as transynaptic, since degenerated axons could not be traced to these locations from the cochlear nerve or trapezoid body. Moreover, biotinylated dextran amine injection in the basal turn of scala media of a normal cochlea labeled cochlear nerve fibers projecting to the high-frequency regions of the cochlear nuclei and to the flocculus, but not to more central auditory nuclei. This is the first detailed account of transynaptic degeneration in the ascending auditory pathway resulting from cochlear damage in an adult mammal. These findings are consistent with a dystrophic process depending on hair-cell loss and/or direct damage to cochlear nerve fibers.
采用瑙塔-拉斯穆森法研究了耳蜗损伤后大脑中终末轴突变性。评估了毛细胞和有髓耳蜗纤维的损失情况。耳蜗拓扑图从蜗顶到蜗底投射在耳蜗核的腹侧到背侧轴上。耳蜗神经纤维和内毛细胞损失的耳蜗拓扑对应性比外毛细胞更好。耳蜗纤维可追踪至耳蜗核的所有部分,包括小细胞层,也可追踪至Y细胞群和绒球。上橄榄复合体、外侧丘系和下丘核中的终末轴突变性被解释为跨突触性的,因为无法从耳蜗神经或斜方体追踪到退变的轴突至这些部位。此外,在正常耳蜗中阶基底转注射生物素化葡聚糖胺标记了投射至耳蜗核高频区域和绒球的耳蜗神经纤维,但未标记至更中枢的听觉核团。这是关于成年哺乳动物耳蜗损伤导致的听觉上行通路跨突触变性的首次详细描述。这些发现与一种依赖于毛细胞损失和/或耳蜗神经纤维直接损伤的营养不良过程一致。