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本文引用的文献

1
Systematic variation of potassium current amplitudes across the tonotopic axis of the rat medial nucleus of the trapezoid body.大鼠梯形体内侧核音频拓扑轴上钾电流幅度的系统性变化。
Hear Res. 2005 Aug;206(1-2):116-32. doi: 10.1016/j.heares.2004.12.012.
2
Hyperpolarization-activated (I) currents in auditory brainstem neurons of normal and congenitally deaf mice.正常和先天性耳聋小鼠听觉脑干神经元中的超极化激活(I)电流
Eur J Neurosci. 2005 Jul;22(1):147-57. doi: 10.1111/j.1460-9568.2005.04185.x.
3
Development of a robust central auditory synapse in congenital deafness.先天性耳聋中强大的中枢听觉突触的发育。
J Neurophysiol. 2005 Nov;94(5):3168-80. doi: 10.1152/jn.00342.2005. Epub 2005 Jul 6.
4
Developmental refinement of inhibitory sound-localization circuits.抑制性声音定位回路的发育完善
Trends Neurosci. 2005 Jun;28(6):290-6. doi: 10.1016/j.tins.2005.04.007.
5
Long-term sensorineural hearing loss induces functional changes in the rat auditory nerve.长期感音神经性听力损失会导致大鼠听觉神经发生功能变化。
Eur J Neurosci. 2004 Dec;20(11):3131-40. doi: 10.1111/j.1460-9568.2004.03809.x.
6
Response properties of single auditory nerve fibers in the mouse.小鼠单根听神经纤维的反应特性
J Neurophysiol. 2005 Jan;93(1):557-69. doi: 10.1152/jn.00574.2004. Epub 2004 Sep 29.
7
Tone frequency maps and receptive fields in the developing chinchilla auditory cortex.发育中的灰鼠听觉皮层中的音调频率图和感受野
J Neurophysiol. 2005 Jan;93(1):454-66. doi: 10.1152/jn.00569.2004. Epub 2004 Sep 1.
8
Presynaptic plasticity at two giant auditory synapses in normal and deaf mice.正常和耳聋小鼠两个巨大听觉突触处的突触前可塑性。
J Physiol. 2004 Nov 1;560(Pt 3):709-19. doi: 10.1113/jphysiol.2004.066662. Epub 2004 Aug 26.
9
Reduced low-voltage activated K+ conductances and enhanced central excitability in a congenitally deaf (dn/dn) mouse.先天性耳聋(dn/dn)小鼠中低电压激活的钾离子电导降低及中枢兴奋性增强
J Physiol. 2004 Aug 15;559(Pt 1):25-33. doi: 10.1113/jphysiol.2004.067421. Epub 2004 Jul 2.
10
The neural basis of temporal processing.时间处理的神经基础。
Annu Rev Neurosci. 2004;27:307-40. doi: 10.1146/annurev.neuro.27.070203.144247.

先天性耳聋会破坏幼年小鼠听觉脑干中的拓扑组织。

Topographic organization in the auditory brainstem of juvenile mice is disrupted in congenital deafness.

作者信息

Leao Richardson N, Sun Hong, Svahn Katarina, Berntson Amy, Youssoufian Monique, Paolini Antonio G, Fyffe Robert E W, Walmsley Bruce

机构信息

Synapse and Hearing Laboratory, Division of Neuroscience, The John Curtin School of Medical Research, The Australian National University, PO Box 334, Canberra, ACT 0200, Australia.

出版信息

J Physiol. 2006 Mar 15;571(Pt 3):563-78. doi: 10.1113/jphysiol.2005.098780. Epub 2005 Dec 22.

DOI:10.1113/jphysiol.2005.098780
PMID:16373385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1805808/
Abstract

There is an orderly topographic arrangement of neurones within auditory brainstem nuclei based on sound frequency. Previous immunolabelling studies in the medial nucleus of the trapezoid body (MNTB) have suggested that there may be gradients of voltage-gated currents underlying this tonotopic arrangement. Here, our electrophysiological and immunolabelling results demonstrate that underlying the tonotopic organization of the MNTB is a combination of medio-lateral gradients of low-and high-threshold potassium currents and hyperpolarization-activated cation currents. Our results also show that the intrinsic membrane properties of MNTB neurones produce a topographic gradient of time delays, which may be relevant to sound localization, following previous demonstrations of the importance of the timing of inhibitory input from the MNTB to the medial superior olive (MSO). Most importantly, we demonstrate that, in the MNTB of congenitally deaf mice, which exhibit no spontaneous auditory nerve activity, the normal tonotopic gradients of neuronal properties are absent. Our results suggest an underlying mechanism for the observed topographic gradient of neuronal firing properties in the MNTB, show that an intrinsic neuronal mechanism is responsible for generating a topographic gradient of time-delays, and provide direct evidence that these gradients rely on spontaneous auditory nerve activity during development.

摘要

基于声音频率,听觉脑干核内的神经元存在有序的拓扑排列。先前在梯形体内侧核(MNTB)进行的免疫标记研究表明,这种音调拓扑排列可能存在电压门控电流梯度。在这里,我们的电生理和免疫标记结果表明,MNTB音调组织的基础是低阈值和高阈值钾电流以及超极化激活阳离子电流的中外侧梯度的组合。我们的结果还表明,MNTB神经元的内在膜特性产生了时间延迟的拓扑梯度,这可能与声音定位有关,此前已有研究表明MNTB向内侧上橄榄核(MSO)的抑制性输入时间很重要。最重要的是,我们证明,在先天性失聪小鼠的MNTB中,由于没有自发的听神经活动,神经元特性的正常音调梯度不存在。我们的结果揭示了MNTB中观察到的神经元放电特性拓扑梯度的潜在机制,表明内在神经元机制负责产生时间延迟的拓扑梯度,并提供了直接证据表明这些梯度在发育过程中依赖于自发的听神经活动。