Motor, somatosensory, and executive cortical areas elicit monosynaptic and polysynaptic neuronal activity in the auditory midbrain

IF 2.5 2区 医学 Q1 AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY Hearing Research Pub Date : 2024-04-16 DOI:10.1016/j.heares.2024.109009
Sarah E Gartside, Bas MJ Olthof, Adrian Rees
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Abstract

We recently reported that the central nucleus of the inferior colliculus (the auditory midbrain) is innervated by glutamatergic pyramidal cells originating not only in auditory cortex (AC), but also in multiple ‘non-auditory’ regions of the cerebral cortex. Here, in anaesthetised rats, we used optogenetics and electrical stimulation, combined with recording in the inferior colliculus to determine the functional influence of these descending connections. Specifically, we determined the extent of monosynaptic excitation and the influence of these descending connections on spontaneous activity in the inferior colliculus.

A retrograde virus encoding both green fluorescent protein (GFP) and channelrhodopsin (ChR2) injected into the central nucleus of the inferior colliculus (ICc) resulted in GFP expression in discrete groups of cells in multiple areas of the cerebral cortex. Light stimulation of AC and primary motor cortex (M1) caused local activation of cortical neurones and increased the firing rate of neurones in ICc indicating a direct excitatory input from AC and M1 to ICc with a restricted distribution. In naïve animals, electrical stimulation at multiple different sites within M1, secondary motor, somatosensory, and prefrontal cortices increased firing rate in ICc. However, it was notable that stimulation at some adjacent sites failed to influence firing at the recording site in ICc. Responses in ICc comprised singular spikes of constant shape and size which occurred with a short, and fixed latency (∼ 5 ms) consistent with monosynaptic excitation of individual ICc units. Increasing the stimulus current decreased the latency of these spikes, suggesting more rapid depolarization of cortical neurones, and increased the number of (usually adjacent) channels on which a monosynaptic spike was seen, suggesting recruitment of increasing numbers of cortical neurons. Electrical stimulation of cortical regions also evoked longer latency, longer duration increases in firing activity, comprising multiple units with spikes occurring with significant temporal jitter, consistent with polysynaptic excitation. Increasing the stimulus current increased the number of spikes in these polysynaptic responses and increased the number of channels on which the responses were observed, although the magnitude of the responses always diminished away from the most activated channels. Together our findings indicate descending connections from motor, somatosensory and executive cortical regions directly activate small numbers of ICc neurones and that this in turn leads to extensive polysynaptic activation of local circuits within the ICc.

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运动、体感和执行皮层区域引发听觉中脑的单突触和多突触神经元活动
我们最近报告说,下丘(听觉中脑)中央核受谷氨酸能锥体细胞支配,这些细胞不仅来自听觉皮层(AC),还来自大脑皮层的多个 "非听觉 "区域。在这里,我们在麻醉大鼠身上使用了光遗传学和电刺激,并结合下丘记录来确定这些降序连接的功能影响。将编码绿色荧光蛋白(GFP)和通道荧光素(ChR2)的逆行病毒注入下丘中央核(ICc)后,GFP在大脑皮层多个区域的离散细胞群中表达。对 AC 和初级运动皮层(M1)的光刺激会引起皮层神经元的局部激活,并提高 ICc 中神经元的发射率,这表明 AC 和 M1 对 ICc 的直接兴奋性输入分布有限。在天真的动物中,对 M1、次级运动、躯体感觉和前额叶皮质中多个不同部位的电刺激会增加 ICc 的发射率。然而,值得注意的是,对一些相邻部位的刺激并不能影响 ICc 中记录部位的发射。ICc 中的反应由形状和大小不变的单个尖峰组成,这些尖峰出现的时间短且潜伏期固定(∼ 5 ms),与单个 ICc 单元的单突触兴奋一致。增加刺激电流会降低这些尖峰的潜伏期,这表明皮质神经元的去极化速度更快,同时会增加出现单突触尖峰的(通常是相邻的)通道数量,这表明皮质神经元的招募数量在增加。对大脑皮层区域的电刺激也会诱发潜伏期更长、持续时间更长的发射活动增加,其中包括多个单位,这些单位的尖峰出现明显的时间抖动,这与多突触兴奋一致。增加刺激电流会增加这些多突触反应中的尖峰数量,并增加可观察到反应的通道数量,尽管反应的幅度总是在远离最活跃通道的地方减弱。我们的研究结果表明,来自运动、躯体感觉和执行皮层区域的降序连接直接激活了少量 ICc 神经元,这反过来又导致了 ICc 内部局部回路的广泛多突触激活。
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来源期刊
Hearing Research
Hearing Research 医学-耳鼻喉科学
CiteScore
5.30
自引率
14.30%
发文量
163
审稿时长
75 days
期刊介绍: The aim of the journal is to provide a forum for papers concerned with basic peripheral and central auditory mechanisms. Emphasis is on experimental and clinical studies, but theoretical and methodological papers will also be considered. The journal publishes original research papers, review and mini- review articles, rapid communications, method/protocol and perspective articles. Papers submitted should deal with auditory anatomy, physiology, psychophysics, imaging, modeling and behavioural studies in animals and humans, as well as hearing aids and cochlear implants. Papers dealing with the vestibular system are also considered for publication. Papers on comparative aspects of hearing and on effects of drugs and environmental contaminants on hearing function will also be considered. Clinical papers will be accepted when they contribute to the understanding of normal and pathological hearing functions.
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