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机构地区:[1]佳木斯医学院附属医院
出 处:《耳鼻喉学报》1999年第1期1-3,共3页
摘 要:定量观察了出生后13个月的先天缺失SOD1基因小鼠的耳蜗毛细胞以及螺旋神经节和疆孔内的神经纤维,并与同龄野生型和出生后2个月的野生型小鼠进行了比较。发现毛细胞和螺旋神经节的缺损约为50%,神经纤维的减少则超过50%。The hair cells,spiral ganglions and nerve fibers in the cochlea were observed in 13 months old knockout mice lacking SOD1gene,which were compared with the same aged wild type mice and 2 months old wild type mice.It was found that the hair cells and gaglion neurons were missing 50%,and the nerve fibers were missing more than 50%in lacking SOD1 gene mice. This suggests that the serious damage in both hair cells and nerve system in the cochlea caused by lacking superoxide dismutase combined by copper and zinc.
关 键 词:毛细胞 神经纤维 螺旋神经节 SOD基因 耳蜗损伤
分 类 号:R764.350.2[医药卫生—耳鼻咽喉科]
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