RAPID CHANGES IN PROTEIN-SYNTHESIS AND CELL-SIZE IN THE COCHLEAR NUCLEUS FOLLOWING 8TH NERVE ACTIVITY BLOCKADE OR COCHLEA ABLATION

被引:108
作者
SIE, KCY
RUBEL, EW
机构
[1] Hearing Development Laboratory, Department of Otolaryngology-Head and Neck Surgery, University of Washington, Seattle, Washington
关键词
DEAFFERENTATION; TRANSSYNAPTIC REGULATION; TETRODOTOXIN; GERBIL;
D O I
10.1002/cne.903200407
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Destruction of the cochlea causes secondary changes in the central auditory pathway through transynaptic regulation. These changes appear to be mediated by an activity-dependent process and can be detected in the avian auditory system as early as 30 minutes after deafferentation. We compared the early changes in cochlear nucleus neurons following deafferentation by cochlea ablation with those seen following activity deprivation by perilymphatic tetrodotoxin (TTX) exposure. Protein synthesis and size of large spherical cells in the anteroventral cochlear nucleus (AVCN) of 14-day-old gerbils were measured during the first 48 hours after the manipulations. Both cochlea ablation and TTX produced a reliable decrease in protein synthesis by AVCN neurons (30-40%) by 1 hour. The magnitude of change in tritiated leucine incorporation was similar at all survival times, in both experimental groups. In contrast to the rapid changes in protein synthesis, the decrease in cell size was first evident 18 hours after TTX exposure and 48 hours after cochlea ablation. There was no significant change in protein synthesis or cell size in control groups at any of the survival times. These findings are consistent with changes in the avian auditory system in response to deafferentation and TTX exposure. Cochlea ablation and TTX exposure induced similar transneuronal changes, supporting the hypotheses that activity of auditory afferents in young mammals plays a regulatory role in the metabolism and morphology of their target neurons in the central auditory pathway, and that early changes following destruction of the peripheral receptor are due to reduction of activity-dependent interactions of presynaptic and postsynaptic cells.
引用
收藏
页码:501 / 508
页数:8
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