TY - JOUR
T1 - Library-based numerical reduction of the Hodgkin - Huxley neuron for network simulation
AU - Sun, Yi
AU - Zhou, Douglas
AU - Rangan, Aaditya V.
AU - Cai, David
N1 - Funding Information:
Acknowledgements The work was supported by NSF grant DMS-0506396 and a grant from the Swartz foundation.
PY - 2009
Y1 - 2009
N2 - We present an efficient library-based numerical method for simulating the Hodgkin - Huxley (HH) neuronal networks. The key components in our numerical method involve (i) a pre-computed high resolution data library which contains typical neuronal trajectories (i.e., the time-courses of membrane potential and gating variables) during the interval of an action potential (spike), thus allowing us to avoid resolving the spikes in detail and to use large numerical time steps for evolving the HH neuron equations; (ii) an algorithm of spike-spike corrections within the groups of strongly coupled neurons to account for spike-spike interactions in a single large time step. By using the library method, we can evolve the HH networks using time steps one order of magnitude larger than the typical time steps used for resolving the trajectories without the library, while achieving comparable resolution in statistical quantifications of the network activity, such as average firing rate, interspike interval distribution, power spectra of voltage traces. Moreover, our large time steps using the library method can break the stability requirement of standard methods (such as Runge-Kutta (RK) methods) for the original dynamics. We compare our library-based method with RK methods, and find that our method can capture very well phase-locked, synchronous, and chaotic dynamics of HH neuronal networks. It is important to point out that, in essence, our library-based HH neuron solver can be viewed as a numerical reduction of the HH neuron to an integrate-and-fire (I&F) neuronal representation that does not sacrifice the gating dynamics (as normally done in the analytical reduction to an I&F neuron).
AB - We present an efficient library-based numerical method for simulating the Hodgkin - Huxley (HH) neuronal networks. The key components in our numerical method involve (i) a pre-computed high resolution data library which contains typical neuronal trajectories (i.e., the time-courses of membrane potential and gating variables) during the interval of an action potential (spike), thus allowing us to avoid resolving the spikes in detail and to use large numerical time steps for evolving the HH neuron equations; (ii) an algorithm of spike-spike corrections within the groups of strongly coupled neurons to account for spike-spike interactions in a single large time step. By using the library method, we can evolve the HH networks using time steps one order of magnitude larger than the typical time steps used for resolving the trajectories without the library, while achieving comparable resolution in statistical quantifications of the network activity, such as average firing rate, interspike interval distribution, power spectra of voltage traces. Moreover, our large time steps using the library method can break the stability requirement of standard methods (such as Runge-Kutta (RK) methods) for the original dynamics. We compare our library-based method with RK methods, and find that our method can capture very well phase-locked, synchronous, and chaotic dynamics of HH neuronal networks. It is important to point out that, in essence, our library-based HH neuron solver can be viewed as a numerical reduction of the HH neuron to an integrate-and-fire (I&F) neuronal representation that does not sacrifice the gating dynamics (as normally done in the analytical reduction to an I&F neuron).
KW - Chaos
KW - Hodgkin - Huxley neuron
KW - Integrate-and-fire neurons
KW - Library method
KW - Neuronal network
KW - Numerical algorithm
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U2 - 10.1007/s10827-009-0151-9
DO - 10.1007/s10827-009-0151-9
M3 - Article
C2 - 19401809
AN - SCOPUS:70350568843
SN - 0929-5313
VL - 27
SP - 369
EP - 390
JO - Journal of Computational Neuroscience
JF - Journal of Computational Neuroscience
IS - 3
ER -