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Gatsby Computational Neuroscience Unit
Alexandra House, 17 Queen Square, LONDON, WC1N 3AR, UK
Tel: +44 (0) 20 7679 1176, Fax +44 (0) 20 7679 1173, admin@gatsby.ucl.ac.uk, www.gatsby.ucl.ac.uk

 

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WORKSHOP ON:
CENTRAL PROBLEMS IN SINGLE CELL COMPUTATION


16-18 September 2002
By invitation only

Venue
B10 Seminar Room, Alexandra House, 17 Queen Square, London, WC1N 3AR


Stochastic integration in neocortical pyramidal neurons in vivo
A. Destexhe, Unite de Neuroscience Integratives et Computationnelles, CNRS, Gif-sur-Yvette, France
Little is known about the integrative properties of central neurons during active states in vivo, despite its functional importance. Here we investigated the integrative properties of neocortical pyramidal neurons in which in vivo conditions were simulated based on intracellular recordings. Neocortical neurons recorded from cat parietal cortex during active states, before and after microperfusion of TTX, show that synaptic background activity accounts for a strong (3-5 fold) decrease of input resistance, a depolarization of approx. 15 mV, and large-amplitude membrane potential fluctuations (std. dev.of approx 3-4 mV). Recording of miniature events in the same cells allowed us to estimate the conditions of release (conductance, frequency, random nature) at excitatory and inhibitory synapses corresponding to active states in vivo. In a second phase, we evaluated the impact of synaptic background activity on integrative properties. We show that high-conductance fluctuations induce a stochastic state in which dendrites are fast-conducting and have facilitated initiation and forward-propagation of Na+-dependent spikes. The probability of evoking a somatic spike is independent of the location of the synaptic input, and is modulable by network activity. Thus, models predict that the integrative mode of neocortical neurons in vivo should be stochastic, fast-conducting, and optimized to process synaptic inputs at high temporal resolution, independently of their position in the dendrites.
Joint work with M. Rudolph (CNRS) and D. Pare (Rutgers University) Supported by CNRS and NIH