Feature extraction of auditory information
听觉信息的特征提取
基本信息
- 批准号:10480231
- 负责人:
- 金额:$ 7.62万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Scientific Research (B).
- 财政年份:1998
- 资助国家:日本
- 起止时间:1998 至 2000
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Sound frequency is coded along the tonotopy in the cochlea, and each ANF has the characteristic frequency. Sound intensity and timing information are coded as a sequence of action potentials. In the avian cochlear nucleus the pathway to extract temporal information starts at Ncl. Magnocellularis (NM) and intensity information at Ncl.Angularis (NA). We have compared the nature of synaptic transmission and postsynaptic membrane excitability in these two nuclei and found target specific differentiation. The membrane excitability of NM is characterized by the presence of both the low threshold voltage activated K+ conductance (LT) and high threshold voltage activated K+ conductance (HT). NM neuron generates a single action potential at the onset of a burst of synaptic inputs or at the beginning of current injection. The neuron in NA is characterized by a regular spike generation in response to current injection or to the burst of synaptic inputs. These neurons do not have LT.K+ currents bu … More t have large quantity of HT K+ currents and Ca2+ activated K+ currents . The frequency of burst firing was reduced by the activity of Ca2+ activated K+ currents. When a train of synaptic inputs were made, the EPSC size depressed drastic in NM neuron while the depression was moderate in NA neuron. By applying a pair of stimulus at various intervals, the NM EPSC depressed in two phases. The first phase is CTZ sensitive, therefore due to desensitization of postsynaptic AMPA receptors, and the 2nd slower phase was CTZ resistive. In NA, EPSC was not affected by CTZ at normal 2mM Ca2+ concentration, however at 5 mM Ca2+ CTZ increased the EPSC size and prolonged decay kinetics as in NM.This might indicate larger quantity of transmitter released from the presynaptic terminals to NM due to larger Ca2+ influx there than to NA.In NM only a few presynaptic terminals are made and they are known as end bulbs of Held, while in NA a large number of small bouton type terminals are formed. Therefore, presynapitc terminals and postsynaptic neurons are likely differentiated target specifically both in morphology and in function. Less
声音频率在耳蜗中沿着音调谱沿着编码,并且每个ANF具有特征频率。声音强度和时间信息被编码为动作电位序列。在鸟类耳蜗核中,提取时间信息的通路始于Ncl。大细胞(NM)和角神经(NA)的强度信息。我们比较了这两个核团的突触传递和突触后膜兴奋性的性质,发现了靶点特异性分化。NM的膜兴奋性表现为同时存在低阈值电压激活的K+电导(LT)和高阈值电压激活的K+电导(HT)。NM神经元在突触输入突发的开始或电流注入开始时产生单个动作电位。NA中的神经元的特征在于响应于电流注入或突触输入的突发而产生规则的尖峰。这些神经元没有LT.K+电流, ...更多信息 HT K+电流和Ca ~(2+)激活的K+电流均不明显。钙激活钾电流的活动降低了爆发放电的频率。当一系列突触输入时,NM神经元EPSC的大小显著降低,NA神经元EPSC的大小则中度降低。在不同的时间间隔内施加一对刺激,可使NM EPSC出现两个时相的抑制。第一个阶段是CTZ敏感的,因此是由于突触后AMPA受体的脱敏,而第二个较慢的阶段是CTZ抵抗的。在正常的2 mM Ca ~(2+)浓度下,CTZ对NA的EPSC无影响,而在5 mM Ca ~(2+)浓度下,CTZ使EPSC增大,衰减动力学延长,这可能表明突触前终末释放到NM的递质比NA的多,这是由于NM的Ca ~(2+)内流比NA的大。而在NA中,形成了大量的小的钮扣型端子。因此,突触前终末和突触后神经元在形态和功能上可能是特异性分化的靶点。少
项目成果
期刊论文数量(44)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Chuhma,N.& Ohmori,H.: "Postmntal development of phase-locked high-fidelity sympaptic coznsmission in the medial nucleus of the trxproid body of the rat" J.Neutoscience. 18・1. 512-520 (1998)
Chuhma, N. 和 Ohmori, H.:“大鼠 trxproid 体内侧核中锁相高保真交感神经的后期发育”J.Neutoscience 18・1 (1998)。
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Chuhma X. & Ohmori H.: "Postnatal Development of phase-locked high-fidelity synaptic transmission in the medial nucleus of the trapezoid body of the rat"J. Neuroscience. 18・1. 512-520 (1998)
Chuhma X. & Ohmori H.:“大鼠梯形体内侧核中相锁高保真突触传递的产后发育”J. Neuroscience 18・1(1998)。
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Funabiki K.,Koyano K.& Ohmori H.: "The role of GABA ergic inputs for coincidence detection in neuvones of nucleus lominaris of the chick"J. Physiology. 508・3. 851-869 (1998)
Funabiki K.、Koyano K. 和 Ohmori H.:“GABA 能输入在雏鸡脑波核神经元中的一致性检测的作用”J. 生理学 508・3(1998)。
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Nao Chuhma,Konomi Koyano and Harunori Ohmori: "Synchronisation of Neurotransmitter Release during Postnatal Development in a Calyceal Presynaptic Terminal."Journal of Physiology. 530.1. 93-104 (2001)
Nao Chuhma、Konomi Koyano 和 Harunori Ohmori:“肾盏突触前末梢产后发育期间神经递质释放的同步”。生理学杂志。
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Ishii MT.,Takano M.,Xie LH.,Noma A. & Ohmori H.: "Moleculor characterization of the hyperpolarization-activated cation channel in rabbit heart sinoatrial node"J. Biol. Chem.. 274. 12835-12839 (1999)
石井 MT.,高野 M.,谢 LH.,野间 A.
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OHMORI Harunori其他文献
OHMORI Harunori的其他文献
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{{ truncateString('OHMORI Harunori', 18)}}的其他基金
Simultaneous recording of electrical activity and fluorescence signal from deep brain tissues by the photometric patch electrode
通过光度贴片电极同时记录深部脑组织的电活动和荧光信号
- 批准号:
26560464 - 财政年份:2014
- 资助金额:
$ 7.62万 - 项目类别:
Grant-in-Aid for Challenging Exploratory Research
Identification of neurons by fluorescence spectrogram through a patch electrode, and the application to auditory neural circuits in vivo
贴片电极荧光光谱识别神经元及其在体内听觉神经回路中的应用
- 批准号:
20220008 - 财政年份:2008
- 资助金额:
$ 7.62万 - 项目类别:
Grant-in-Aid for Scientific Research (S)
Auditory Feature Extraction and Processing
听觉特征提取和处理
- 批准号:
17023027 - 财政年份:2005
- 资助金额:
$ 7.62万 - 项目类别:
Grant-in-Aid for Scientific Research on Priority Areas
A method of introducing large molecules into neurons.
一种将大分子引入神经元的方法。
- 批准号:
09558103 - 财政年份:1997
- 资助金额:
$ 7.62万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Regulatory mechonisms for pxocytosis
胞吐作用的调节机制
- 批准号:
08457011 - 财政年份:1996
- 资助金额:
$ 7.62万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Identification of Neurotransmitter released from hair cells
鉴定毛细胞释放的神经递质
- 批准号:
06454713 - 财政年份:1994
- 资助金额:
$ 7.62万 - 项目类别:
Grant-in-Aid for General Scientific Research (B)
Application of a UV-laser to a confocal microscope and the observation of intracellular Ca2+dynamics.
紫外激光在共焦显微镜上的应用和细胞内 Ca2 动力学的观察。
- 批准号:
04507001 - 财政年份:1992
- 资助金额:
$ 7.62万 - 项目类别:
Grant-in-Aid for Developmental Scientific Research (A)
Study for the dynamics of the intracellular Ca concentration changes with high spatial and temporal resolution.
研究具有高空间和时间分辨率的细胞内 Ca 浓度变化的动态。
- 批准号:
02557007 - 财政年份:1990
- 资助金额:
$ 7.62万 - 项目类别:
Grant-in-Aid for Developmental Scientific Research (B)
Study of synaptic transmissions on hair cells
毛细胞突触传递的研究
- 批准号:
01440021 - 财政年份:1989
- 资助金额:
$ 7.62万 - 项目类别:
Grant-in-Aid for General Scientific Research (A)
Development of fluorometric microscope system and its application to intracellular Ca^<2+> measurements in neurons
荧光显微镜系统的研制及其在神经元细胞内Ca^2测量中的应用
- 批准号:
62870005 - 财政年份:1987
- 资助金额:
$ 7.62万 - 项目类别:
Grant-in-Aid for Developmental Scientific Research
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