TY - JOUR
T1 - An efficient population density method for modeling neural networks with synaptic dynamics manifesting finite relaxation time and short-term plasticity
AU - Huang, Chih Hsu
AU - Lin, Chou Ching K.
N1 - Funding Information:
This work was supported by the National Cheng Kung University Hospital and funded by a grant (MOST 105-2314-B-006-080-MY3) from the Ministry of Science and Technology, Taiwan. Correspondence should be addressed to Chou-Ching K. Lin, Department of Neurology, National Cheng Kung University Hospital, 138 Sheng Li Road, Tainan, Taiwan 70403, E-mail: cxl45@mail.ncku.edu.tw. https://doi.org/10.1523/ENEURO.0002-18.2018 Copyright © 2018 Huang and Lin This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
Publisher Copyright:
© 2018 Huang and Lin.
PY - 2018/11/1
Y1 - 2018/11/1
N2 - When incorporating more realistic synaptic dynamics, the computational efficiency of population density methods (PDMs) declines sharply due to the increase in the dimension of master equations. To avoid such a decline, we develop an efficient PDM, termed colored-synapse PDM (csPDM), in which the dimension of the master equations does not depend on the number of synapse-associated state variables in the underlying network model. Our goal is to allow the PDM to incorporate realistic synaptic dynamics that possesses not only finite relaxation time but also short-term plasticity (STP). The model equations of csPDM are derived based on the diffusion approximation on synaptic dynamics and probability density function methods for Langevin equations with colored noise. Numerical examples, given by simulations of the population dynamics of uncoupled exponential integrate-andfire (EIF) neurons, show good agreement between the results of csPDM and Monte Carlo simulations (MCSs). Compared to the original full-dimensional PDM (fdPDM), the csPDM reveals more excellent computational efficiency because of the lower dimension of the master equations. In addition, it permits network dynamics to possess the short-term plastic characteristics inherited from plastic synapses. The novel csPDM has potential applicability to any spiking neuron models because of no assumptions on neuronal dynamics, and, more importantly, this is the first report of PDM to successfully encompass short-term facilitation/depression properties.
AB - When incorporating more realistic synaptic dynamics, the computational efficiency of population density methods (PDMs) declines sharply due to the increase in the dimension of master equations. To avoid such a decline, we develop an efficient PDM, termed colored-synapse PDM (csPDM), in which the dimension of the master equations does not depend on the number of synapse-associated state variables in the underlying network model. Our goal is to allow the PDM to incorporate realistic synaptic dynamics that possesses not only finite relaxation time but also short-term plasticity (STP). The model equations of csPDM are derived based on the diffusion approximation on synaptic dynamics and probability density function methods for Langevin equations with colored noise. Numerical examples, given by simulations of the population dynamics of uncoupled exponential integrate-andfire (EIF) neurons, show good agreement between the results of csPDM and Monte Carlo simulations (MCSs). Compared to the original full-dimensional PDM (fdPDM), the csPDM reveals more excellent computational efficiency because of the lower dimension of the master equations. In addition, it permits network dynamics to possess the short-term plastic characteristics inherited from plastic synapses. The novel csPDM has potential applicability to any spiking neuron models because of no assumptions on neuronal dynamics, and, more importantly, this is the first report of PDM to successfully encompass short-term facilitation/depression properties.
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U2 - 10.1523/ENEURO.0002-18.2018
DO - 10.1523/ENEURO.0002-18.2018
M3 - Article
C2 - 30662939
AN - SCOPUS:85060169821
VL - 5
JO - eNeuro
JF - eNeuro
SN - 2373-2822
IS - 6
M1 - e0002
ER -