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本文引用的文献

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Activation of Distinct Channelrhodopsin Variants Engages Different Patterns of Network Activity.不同通道型视紫红质变体的激活会引发不同的网络活动模式。
eNeuro. 2020 Jan 3;7(1). doi: 10.1523/ENEURO.0222-18.2019. Print 2020 Jan/Feb.
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Neural Recording and Modulation Technologies.神经记录与调制技术
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Dual color optogenetic control of neural populations using low-noise, multishank optoelectrodes.使用低噪声多通道光电极对神经群体进行双色光遗传学控制。
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An Upconversion Nanoparticle Enables Near Infrared-Optogenetic Manipulation of the Caenorhabditis elegans Motor Circuit.上转换纳米粒子实现了利用近红外光遗传操控秀丽隐杆线虫的运动回路。
ACS Nano. 2019 Mar 26;13(3):3373-3386. doi: 10.1021/acsnano.8b09270. Epub 2019 Jan 29.
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Molecular tools for imaging and recording neuronal activity.用于成像和记录神经元活动的分子工具。
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Ultrafast optogenetic stimulation of the auditory pathway by targeting-optimized Chronos.靶向优化 Chronos 实现听觉通路的超快光遗传学刺激。
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Crystal structure of the red light-activated channelrhodopsin Chrimson.红光激活通道蛋白 Chrimson 的晶体结构。
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8
Specificity, Versatility, and Continual Development: The Power of Optogenetics for Epilepsy Research.特异性、多功能性与持续发展:光遗传学在癫痫研究中的力量
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Temporal processing and context dependency in response to mechanosensation.对机械感觉反应的时间处理和语境相关性。
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10
Theoretical analysis of low-power fast optogenetic control of firing of Chronos-expressing neurons.表达Chronos的神经元放电的低功率快速光遗传学控制的理论分析
Neurophotonics. 2018 Apr;5(2):025009. doi: 10.1117/1.NPh.5.2.025009. Epub 2018 May 24.

表达红移超快视紫红质的神经元高频光遗传学尖峰放电的理论优化

Theoretical optimization of high-frequency optogenetic spiking of red-shifted very fast-Chrimson-expressing neurons.

作者信息

Gupta Neha, Bansal Himanshu, Roy Sukhdev

机构信息

Dayalbagh Educational Institute, Department of Physics and Computer Science, Agra, India.

出版信息

Neurophotonics. 2019 Apr;6(2):025002. doi: 10.1117/1.NPh.6.2.025002. Epub 2019 Apr 11.

DOI:10.1117/1.NPh.6.2.025002
PMID:31001567
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6458485/
Abstract

A detailed theoretical analysis and optimization of high-fidelity, high-frequency firing of the red-shifted very-fast-Chrimson (vf-Chrimson) expressing neurons is presented. A four-state model for vf-Chrimson photocycle has been formulated and incorporated in Hodgkin-Huxley and Wang-Buzsaki spiking neuron circuit models. The effect of various parameters that include irradiance, pulse width, frequency, expression level, and membrane capacitance has been studied in detail. Theoretical simulations are in excellent agreement with recently reported experimental results. The analysis and optimization bring out additional interesting features. A minimal pulse width of 1.7 ms at induces a peak photocurrent of 1250 pA. Optimal irradiance ( ) and pulse width ( ) to trigger action potential have been determined. At frequencies beyond 200 Hz, higher values of expression level and irradiance result in spike failure. Singlet and doublet spiking fidelity can be maintained up to 400 and 150 Hz, respectively. The combination of expression level and membrane capacitance is a crucial factor to achieve high-frequency firing above 500 Hz. Its optimization enables 100% spike probability of up to 1 kHz. The study is useful in designing new high-frequency optogenetic neural spiking experiments with desired spatiotemporal resolution, by providing insights into the temporal spike coding, plasticity, and curing neurodegenerative diseases.

摘要

本文对表达红移超快Chrimson(vf-Chrimson)的神经元进行高保真、高频放电的详细理论分析和优化。已构建vf-Chrimson光循环的四态模型,并将其纳入霍奇金-赫胥黎和王-布萨克脉冲神经元电路模型。详细研究了包括辐照度、脉冲宽度、频率、表达水平和膜电容等各种参数的影响。理论模拟与最近报道的实验结果高度吻合。该分析和优化还揭示了其他有趣的特征。在 时,最小脉冲宽度为1.7毫秒可诱导出1250皮安的峰值光电流。已确定触发动作电位的最佳辐照度( )和脉冲宽度( )。在频率超过200赫兹时,较高的表达水平和辐照度会导致脉冲失败。单脉冲和双脉冲放电保真度分别可维持到400赫兹和150赫兹。表达水平和膜电容的组合是实现500赫兹以上高频放电的关键因素。对其进行优化可使高达1千赫兹的脉冲概率达到100%。该研究通过深入了解时间脉冲编码、可塑性和治疗神经退行性疾病,有助于设计具有所需时空分辨率的新型高频光遗传学神经脉冲实验。