Staecker H, Kopke R, Malgrange B, Lefebvre P, Van de Water T R
Department of Otolaryngology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Neuroreport. 1996 Mar 22;7(4):889-94. doi: 10.1097/00001756-199603220-00011.
Destruction of auditory hair cells results in a subsequent loss of auditory neurons. In situ hybridization and neuronal cell culture studies as well as analyses of the inner ears of neurotrophin and neurotrophin receptor gene knockout mice have shown that NT-3 and BDNF mediate both the development and survival of auditory neurons. In this study guinea pigs were exposed to the ototoxic combination of an aminoglycoside antibiotic and a loop diuretic and then received 8 weeks of intracochlear infusion of either NT-3, BDNF or NT-3 + BDNF to determine whether site-specific application of these neurotrophins could prevent the loss of auditory neurons that follows a loss of auditory hair cells. Infusion of either NT-3 or NT-3 + BDNF into the scala tympani resulted in a > 90% survival of auditory neurons while BDNF infusion yielded a 78% survival rate, compared with a 14-24% neuronal survival rate in untreated ototoxin-exposed cochleae. These results show that loss of auditory neurons that occurs subsequent to a loss of auditory hair cells can be prevented by in vivo neurotrophin therapy with either NT-3 or BDNF.
听觉毛细胞的破坏会导致随后听觉神经元的丧失。原位杂交、神经元细胞培养研究以及对神经营养因子和神经营养因子受体基因敲除小鼠内耳的分析表明,NT-3和BDNF介导听觉神经元的发育和存活。在本研究中,豚鼠暴露于氨基糖苷类抗生素和袢利尿剂的耳毒性组合,然后接受8周的耳蜗内输注NT-3、BDNF或NT-3 + BDNF,以确定这些神经营养因子的位点特异性应用是否可以预防听觉毛细胞丧失后听觉神经元的丧失。与未治疗的暴露于耳毒素的耳蜗中14-24%的神经元存活率相比,向鼓阶内输注NT-3或NT-3 + BDNF可使听觉神经元的存活率>90%,而输注BDNF的存活率为78%。这些结果表明,听觉毛细胞丧失后发生的听觉神经元丧失可以通过用NT-3或BDNF进行体内神经营养因子治疗来预防。