4.7 Article

Frequency-Dependent Energy Demand of Dendritic Responses to Deep Brain Stimulation in Thalamic Neurons: A Model-Based Study

出版社

IEEE-INST ELECTRICAL ELECTRONICS ENGINEERS INC
DOI: 10.1109/TNNLS.2020.3009293

关键词

Neurons; Satellite broadcasting; Computational modeling; Ions; Relays; Electrodes; Brain modeling; Computational model; deep brain stimulation (DBS); dendritic activity; metabolic energy; thalamocortical (TC) relay neuron

资金

  1. National Natural Science Foundation of China [61601320]
  2. Tianjin Municipal Natural Science Foundation [19JCQNJC01200]
  3. Tianjin University PEIYANG Scholar-Reserved Academic Program [2019XRG-0051]

向作者/读者索取更多资源

This study estimated the energy demand associated with dendritic responses to thalamic DBS by simulating dendritic activity in TC relay neurons. The ATP demand of dendritic activity was found to be frequency dependent and influenced by factors such as antidromic activation and synaptic inputs.
Thalamic deep brain stimulation (DBS) generates excitatory postsynaptic currents and action potentials (APs) by triggering large numbers of synaptic inputs to local cells, which also activates axonal spikes to antidromically invade the soma and dendrites. To maintain signaling, the evoked dendritic responses require metabolic energy to restore ion gradients in each dendrite. The objective of this study is to estimate the energy demand associated with dendritic responses to thalamic DBS. We use a morphologically realistic computational model to simulate dendritic activity in thalamocortical (TC) relay neurons with axonal intracellular stimulation or DBS-like extracellular stimulation. We determine the metabolic cost by calculating the number of adenosine triphosphate (ATP) expended to pump Na+ and Ca2+ ions out of each dendrite. The ATP demand of dendritic activity exhibits frequency dependence, which is determined by the number of spikes in the dendrites. Each backpropagating AP from the soma activates a spike in the dendrites, and the dendritic firing is dominated by antidromic activation of the soma. High stimulus frequencies decrease dendritic ATP cost by reducing the fidelity of antidromic activation. Synaptic inputs and stimulus-induced polarization govern the ATP cost of dendritic responses by facilitating/suppressing antidromic activation, which also influences the ATP cost by depolarizing/hyperpolarizing each dendrite. These findings are important for understanding the synaptic signaling energy in TC relay neurons and metabolism-dependent functional imaging data of thalamic DBS.

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