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J Comput Neurosci ; 27(2): 161-76, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19172386

ABSTRACT

The accurate simulation of a neuron's ability to integrate distributed synaptic input typically requires the simultaneous solution of tens of thousands of ordinary differential equations. For, in order to understand how a cell distinguishes between input patterns we apparently need a model that is biophysically accurate down to the space scale of a single spine, i.e., 1 mum. We argue here that one can retain this highly detailed input structure while dramatically reducing the overall system dimension if one is content to accurately reproduce the associated membrane potential at a small number of places, e.g., at the site of action potential initiation, under subthreshold stimulation. The latter hypothesis permits us to approximate the active cell model with an associated quasi-active model, which in turn we reduce by both time-domain (Balanced Truncation) and frequency-domain (H(2) approximation of the transfer function) methods. We apply and contrast these methods on a suite of typical cells, achieving up to four orders of magnitude in dimension reduction and an associated speed-up in the simulation of dendritic democratization and resonance. We also append a threshold mechanism and indicate that this reduction has the potential to deliver an accurate quasi-integrate and fire model.


Subject(s)
Cell Membrane/physiology , Central Nervous System/physiology , Computer Simulation , Membrane Potentials/physiology , Neurons/physiology , Synaptic Transmission/physiology , Action Potentials/physiology , Algorithms , Animals , Axons/physiology , Dendrites/physiology , Humans , Ion Channels/physiology , Kinetics , Linear Models , Neural Pathways/physiology , Rats
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