Voltage-gated sodium channel expression in rat spiral ganglion neurons

被引:30
作者
Fryatt, A. G. [1 ]
Vial, C. [1 ]
Mulheran, M. [1 ]
Gunthorpe, M. J. [2 ]
Grubb, B. D. [1 ]
机构
[1] Univ Leicester, Dept Cell Physiol & Pharmacol, Leicester LE1 9HN, Leics, England
[2] GlaxoSmithKline Res & Dev Ltd, Neurosci Ctr Excellence Drug Discovery, Harlow CM19 5AW, Essex, England
基金
英国生物技术与生命科学研究理事会;
关键词
Cochlea; Immunohistochemistry; Peripherin; RT-PCR; Spiral ganglion neurons; Voltage-gated sodium channels; DORSAL-ROOT GANGLIA; PERIPHERAL NERVOUS-SYSTEM; SENSORY NEURONS; MESSENGER-RNAS; ALPHA-SUBUNIT; UP-REGULATION; HEARING-LOSS; INNER-EAR; PAIN; TINNITUS;
D O I
10.1016/j.mcn.2009.09.001
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
The spiral ganglion neurons (SGN) provide the afferent innervation of the hair cells in the organ of Corti and relay auditory information from the inner ear to the brain. Voltage-gated sodium channels (Na-V) initiate and propagate action potentials that encode this sensory information but little is known regarding the subtypes expressed in these cells. We have used RT-PCR and immunohistochemistry to study the compliment and anatomical distribution of Na-V channels in rodent SGN. Na(V)1.1, Na(V)1.6 and Na(V)1.7 were all detected at the mRNA level. Fluorescence or streptavidin-horseradish peroxidase immunohistochemistry extended these findings, demonstrating predominant localisation of Na(V)1.6 and Na(V)1.7 on SCN cell bodies and Na(V)1.1 on axonal processes. Dual labelling with peripherin demonstrated higher Na(V)1.6 and Na(V)1.7 expression on Type I rather than Type II neurons. These results provide evidence for selective expression and variations in the distribution of VGSC in the rodent SGN, which may guide further studies into afferent function in the auditory pathway and therapeutic approaches for diseases such as hearing loss and tinnitus. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:399 / 407
页数:9
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