Energetics of stochastic BCM type synaptic plasticity and storing of accurate information.

IF 1.5 4区 医学 Q3 MATHEMATICAL & COMPUTATIONAL BIOLOGY
Journal of Computational Neuroscience Pub Date : 2021-05-01 Epub Date: 2021-02-02 DOI:10.1007/s10827-020-00775-0
Jan Karbowski
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引用次数: 5

Abstract

Excitatory synaptic signaling in cortical circuits is thought to be metabolically expensive. Two fundamental brain functions, learning and memory, are associated with long-term synaptic plasticity, but we know very little about energetics of these slow biophysical processes. This study investigates the energy requirement of information storing in plastic synapses for an extended version of BCM plasticity with a decay term, stochastic noise, and nonlinear dependence of neuron's firing rate on synaptic current (adaptation). It is shown that synaptic weights in this model exhibit bistability. In order to analyze the system analytically, it is reduced to a simple dynamic mean-field for a population averaged plastic synaptic current. Next, using the concepts of nonequilibrium thermodynamics, we derive the energy rate (entropy production rate) for plastic synapses and a corresponding Fisher information for coding presynaptic input. That energy, which is of chemical origin, is primarily used for battling fluctuations in the synaptic weights and presynaptic firing rates, and it increases steeply with synaptic weights, and more uniformly though nonlinearly with presynaptic firing. At the onset of synaptic bistability, Fisher information and memory lifetime both increase sharply, by a few orders of magnitude, but the plasticity energy rate changes only mildly. This implies that a huge gain in the precision of stored information does not have to cost large amounts of metabolic energy, which suggests that synaptic information is not directly limited by energy consumption. Interestingly, for very weak synaptic noise, such a limit on synaptic coding accuracy is imposed instead by a derivative of the plasticity energy rate with respect to the mean presynaptic firing, and this relationship has a general character that is independent of the plasticity type. An estimate for primate neocortex reveals that a relative metabolic cost of BCM type synaptic plasticity, as a fraction of neuronal cost related to fast synaptic transmission and spiking, can vary from negligible to substantial, depending on the synaptic noise level and presynaptic firing.

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随机BCM型突触可塑性的能量学与准确信息的存储。
皮层回路中的兴奋性突触信号被认为是代谢昂贵的。两个基本的大脑功能,学习和记忆,与长期的突触可塑性有关,但我们对这些缓慢的生物物理过程的能量学知之甚少。本研究探讨了具有衰减项、随机噪声和神经元放电速率对突触电流的非线性依赖(适应)的扩展版BCM可塑性中信息存储的能量需求。结果表明,该模型的突触权重具有双稳定性。为了对系统进行解析分析,将其简化为种群平均塑性突触电流的简单动态平均场。接下来,利用非平衡热力学的概念,我们推导出塑性突触的能量率(熵产率)和相应的用于编码突触前输入的Fisher信息。这种能量来源于化学,主要用于对抗突触权重和突触前放电率的波动,它随着突触权重的增加而急剧增加,随着突触前放电率的增加而更加均匀,尽管这是非线性的。在突触双稳定性开始时,Fisher信息和记忆寿命都急剧增加,增加了几个数量级,但可塑性能率仅发生轻微变化。这意味着存储信息精度的巨大提高并不需要消耗大量的代谢能量,这表明突触信息不受能量消耗的直接限制。有趣的是,对于非常弱的突触噪声,这种对突触编码精度的限制是由可塑性能率相对于突触前平均放电的导数施加的,这种关系具有独立于可塑性类型的一般特征。对灵长类动物新皮层的估计表明,BCM型突触可塑性的相对代谢成本,作为与快速突触传递和尖峰相关的神经元成本的一部分,可以从微不足道到很大,这取决于突触噪声水平和突触前放电。
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来源期刊
CiteScore
2.00
自引率
8.30%
发文量
32
审稿时长
3 months
期刊介绍: The Journal of Computational Neuroscience provides a forum for papers that fit the interface between computational and experimental work in the neurosciences. The Journal of Computational Neuroscience publishes full length original papers, rapid communications and review articles describing theoretical and experimental work relevant to computations in the brain and nervous system. Papers that combine theoretical and experimental work are especially encouraged. Primarily theoretical papers should deal with issues of obvious relevance to biological nervous systems. Experimental papers should have implications for the computational function of the nervous system, and may report results using any of a variety of approaches including anatomy, electrophysiology, biophysics, imaging, and molecular biology. Papers investigating the physiological mechanisms underlying pathologies of the nervous system, or papers that report novel technologies of interest to researchers in computational neuroscience, including advances in neural data analysis methods yielding insights into the function of the nervous system, are also welcomed (in this case, methodological papers should include an application of the new method, exemplifying the insights that it yields).It is anticipated that all levels of analysis from cognitive to cellular will be represented in the Journal of Computational Neuroscience.
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