Volume 8 Supplement 2
Constraining neural microcircuits with surrogate physiological data and genetic algorithms
© Eager et al; licensee BioMed Central Ltd. 2007
Published: 6 July 2007
Biophysically detailed bottom-up approaches to modelling neural networks have previously used simulated annealing, gradient-decent or ad-hoc algorithms to constrain the many free parameters . This study explores the use of genetic algorithms to automatically search for a known configuration using extracellular spike recordings or intracellular voltage data. Surrogate data on neural responses is generated and the ability of the algorithms to find the (known) neural parameters is assessed.
Materials and methods
Four cell subtypes, in a known microcircuit of the mammalian cochlear nucleus , are simulated in a network with 60 frequency channels of auditory input. Each cell received a 'tonotopic' projection of auditory nerve fibres, simulated using a phenomenological auditory nerve model response to a 60 dB SPL notch noise stimuli. Single compartment Hodgkin-Huxley neurons and conductance synapses were implemented in NEURON. Detailed equations for the active voltage-dependant currents INa, IKHT, IKLT, IKA and Ih, were derived from in vitro studies of cochlear nucleus cells . Using genetic algorithm optimisation, four cost functions using identical input stimuli were investigated. The cost functions calculated error in either: (i) absolute spike times, (ii) peri-stimulus time histograms, (iii) cumulative spike counts, or (iv) average intracellular voltages for each cell in the network. Network parameters controlling the number, weight and distribution of the synaptic connections were used in the optimisation, but these could easily be extended to incorporate other cell properties. In all, 30 parameters controlling 10 synaptic connections were converted to a GA binary string.
Genetic Algorithm Cost Function Performance
1Best GA Score
Mean Top 100 2
Success of the GA optimization was affected by intrinsic noise in the neural model and depended on the sensitivity of the cost function to changes in each parameter. The results have shown the potential of genetic algorithms to constrain the underlying synaptic parameters of BNNs from any of the chosen sources of physiological data. More work is needed to assess the impact of reducing the amount of information available to the cost function and setting confidence limits for each parameter.
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This article is published under license to BioMed Central Ltd.