Model of the HVC neural network as a song motor in zebra finch.

IF 2.1 4区 医学 Q2 MATHEMATICAL & COMPUTATIONAL BIOLOGY
Frontiers in Computational Neuroscience Pub Date : 2024-11-20 eCollection Date: 2024-01-01 DOI:10.3389/fncom.2024.1417558
Pan Xia, Henry D I Abarbanel
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引用次数: 0

Abstract

The nucleus HVC within the avian song system produces crystalized instructions which lead to precise, learned vocalization in zebra finches (Taeniopygia guttata). This paper proposes a model of the HVC neural network based on the physiological properties of individual HVC neurons, their synaptic interactions calibrated by experimental measurements, as well as the synaptic signal into this region which triggers song production. This neural network model comprises of two major neural populations in this area: neurons projecting to the nucleus RA and interneurons. Each single neuron model of HVCRA is constructed with conductance-based ion currents of fast Na+ and K+ and a leak channel, while the interneuron model includes extra transient Ca2+ current and hyperpolarization-activated inward current. The synaptic dynamics is formed with simulated delivered neurotransmitter pulses from presynaptic cells and neurotransmitter receptor opening rates of postsynaptic neurons. We show that this network model qualitatively exhibits observed electrophysiological behaviors of neurons independent or in the network, as well as the importance of bidirectional interactions between the HVCRA neuron and the HVCI neuron. We also simulate the pulse input from A11 neuron group to HVC. This signal successfully suppresses the interneuron, which leads to sequential firing of projection neurons that matches measured burst onset, duration, and spike quantities during the zebra finch motif. The result provides a biophysically based model characterizing the dynamics and functions of the HVC neural network as a song motor, and offers a reference for synaptic coupling strength in the avian brain.

斑胸草雀HVC神经网络作为鸣叫运动的模型。
鸟类鸣叫系统中的核HVC产生结晶指令,导致斑马雀(Taeniopygia guttata)精确的、习得的发声。本文基于单个HVC神经元的生理特性、实验测量校准的突触相互作用以及进入该区域触发歌曲产生的突触信号,提出了一个HVC神经网络模型。该神经网络模型由两个主要的神经群组成:向RA核投射的神经元和中间神经元。HVCRA的单个神经元模型由基于电导的快速Na+和K+离子电流和泄漏通道构建,而中间神经元模型包括额外的瞬态Ca2+电流和超极化激活的内向电流。突触动力学是通过模拟突触前细胞传递的神经递质脉冲和突触后神经元的神经递质受体打开率形成的。我们表明,该网络模型定性地展示了观察到的神经元独立或在网络中的电生理行为,以及HVCRA神经元和HVCI神经元之间双向相互作用的重要性。我们还模拟了A11神经元组对HVC的脉冲输入。该信号成功地抑制了中间神经元,从而导致投射神经元的连续放电,这与在斑胸草雀motif期间测量到的突发发作、持续时间和峰值数量相匹配。该结果提供了一个基于生物物理的模型来表征HVC神经网络作为一种歌唱运动的动力学和功能,并为鸟类大脑突触耦合强度提供了参考。
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来源期刊
Frontiers in Computational Neuroscience
Frontiers in Computational Neuroscience MATHEMATICAL & COMPUTATIONAL BIOLOGY-NEUROSCIENCES
CiteScore
5.30
自引率
3.10%
发文量
166
审稿时长
6-12 weeks
期刊介绍: Frontiers in Computational Neuroscience is a first-tier electronic journal devoted to promoting theoretical modeling of brain function and fostering interdisciplinary interactions between theoretical and experimental neuroscience. Progress in understanding the amazing capabilities of the brain is still limited, and we believe that it will only come with deep theoretical thinking and mutually stimulating cooperation between different disciplines and approaches. We therefore invite original contributions on a wide range of topics that present the fruits of such cooperation, or provide stimuli for future alliances. We aim to provide an interactive forum for cutting-edge theoretical studies of the nervous system, and for promulgating the best theoretical research to the broader neuroscience community. Models of all styles and at all levels are welcome, from biophysically motivated realistic simulations of neurons and synapses to high-level abstract models of inference and decision making. While the journal is primarily focused on theoretically based and driven research, we welcome experimental studies that validate and test theoretical conclusions. Also: comp neuro
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