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首页> 外文期刊>Journal of Computational Neuroscience >Spiking resonances in models with the same slow resonant and fast amplifying currents but different subthreshold dynamic properties
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Spiking resonances in models with the same slow resonant and fast amplifying currents but different subthreshold dynamic properties

机译:具有相同的慢速谐振电流和快速放大电流,但具有不同的亚阈值动态特性的模型中的尖峰谐振

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摘要

The generation of spiking resonances in neurons (preferred spiking responses to oscillatory inputs) requires the interplay of the intrinsic ionic currents that operate at the subthreshold voltage level and the spiking mechanisms. Combinations of the same types of ionic currents in different parameter regimes may give rise to different types of nonlinearities in the voltage equation (e.g., parabolic- and cubic-like), generating subthreshold (membrane potential) oscillations patterns with different properties. These nonlinearities are not apparent in the model equations, but can be uncovered by plotting the voltage nullclines in the phase-plane diagram. We investigate the spiking resonant properties of conductance-based models that are biophysically equivalent at the subthreshold level (same ionic currents), but dynamically different (parabolic- and cubic-like voltage nullclines). As a case study we consider a model having a persistent sodium and a hyperpolarization-activated (h-) currents, which exhibits subthreshold resonance in the theta frequency band. We unfold the concept of spiking resonance into evoked and output spiking resonance. The former focuses on the input frequencies that are able to generate spikes, while the latter focuses on the output spiking frequencies regardless of the input frequency that generated these spikes. A cell can exhibit one or both types of resonances. We also measure spiking phasonance, which is an extension of subthreshold phasonance (zero-phase-shift response to oscillatory inputs) to the spiking regime. The subthreshold resonant properties of both types of models are communicated to the spiking regime for low enough input amplitudes as the voltage response for the subthreshold resonant frequency band raises above threshold. For higher input amplitudes evoked spiking resonance is no longer present in these models, but output spiking resonance is present primarily in the parabolic-like model due to a cycle skipping mechanism (involving mixed-mode oscillations), while the cubic-like model shows a better 1:1 entrainment. We use dynamical systems tools to explain the underlying mechanisms and the mechanistic differences between the resonance types. Our results demonstrate that the effective time scales that operate at the subthreshold regime to generate intrinsic subthreshold oscillations, mixed-mode oscillations and subthreshold resonance do not necessarily determine the existence of a preferred spiking response to oscillatory inputs in the same frequency band. The results discussed in this paper highlight both the complexity of the suprathreshold responses to oscillatory inputs in neurons having resonant and amplifying currents with different time scales and the fact that the identity of the participating ionic currents is not enough to predict the resulting patterns, but additional dynamic information, captured by the geometric properties of the phase-space diagram, is needed.
机译:在神经元中产生尖峰共振(最好是对振荡输入的尖峰响应)需要在低于阈值电压水平工作的固有离子电流和尖峰机制的相互作用。不同参数范围内相同类型离子电流的组合可能会导致电压方程式(例如抛物线形和立方形)中的非线性类型不同,从而产生具有不同特性的亚阈值(膜电位)振荡模式。这些非线性在模型方程中并不明显,但是可以通过在相平面图中绘制电压零线来发现。我们研究了基于电导的模型的尖峰共振特性,这些模型在亚阈值水平(相同的离子电流)在生物物理上是等效的,但是动态地不同(抛物线型和立方型电压零线)。作为案例研究,我们考虑具有持久钠和超极化激活(h-)电流的模型,该模型在theta频带中表现出亚阈值共振。我们将尖峰共鸣的概念展开为诱发和输出尖峰共鸣。前者着重于能够产生尖峰的输入频率,而后者着重于输出尖峰频率,而不管产生这些尖峰的输入频率如何。细胞可以表现出一种或两种类型的共振。我们还测量了尖峰相声,它是亚阈值相声(对振荡输入的零相移响应)到尖峰状态的扩展。当亚阈值共振频带的电压响应升高到阈值以上时,两种类型的模型的亚阈值共振特性将传递给尖峰区域,以获得足够低的输入幅度。对于更高的输入振幅,这些模型中不再存在诱发尖峰共振,但是由于周期跳跃机制(涉及混合模式振荡),输出尖峰共振主要出现在抛物线样模型中,而立方样模型则显示出更好的1:1夹带。我们使用动力学系统工具来解释共振类型之间的潜在机理和机理差异。我们的结果表明,在亚阈值范围内运行以产生固有亚阈值振荡,混合模式振荡和亚阈值谐振的有效时间标度并不一定确定在相同频带中存在对振荡输入的优选尖峰响应。本文讨论的结果既凸显了具有不同时间尺度的共振和放大电流的神经元中对振荡输入的超阈值响应的复杂性,又是参与的离子电流的身份不足以预测所得模式的事实,但是另外需要由相空间图的几何属性捕获的动态信息。

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