Sensory experience modifies spontaneous state dynamics in a large-scale barrel cortical model.

Experimental evidence suggests that spontaneous neuronal activity may shape and be shaped by sensory experience. However, we lack information on how sensory experience modulates the underlying synaptic dynamics and how such modulation influences the response of the network to future events. Here we study whether spike-timing-dependent plasticity (STDP) can mediate sensory-induced modifications in the spontaneous dynamics of a new large-scale model of layers II, III and IV of the rodent barrel cortex. Our model incorporates significant physiological detail, including the types of neurons present, the probabilities and delays of connections, and the STDP profiles at each excitatory synapse. We stimulated the neuronal network with a protocol of repeated sensory inputs resembling those generated by the protraction-retraction motion of whiskers when rodents explore their environment, and studied the changes in network dynamics. By applying dimensionality reduction techniques to the synaptic weight space, we show that the initial spontaneous state is modified by each repetition of the stimulus and that this reverberation of the sensory experience induces long-term, structured modifications in the synaptic weight space. The post-stimulus spontaneous state encodes a memory of the stimulus presented, since a different dynamical response is observed when the network is presented with shuffled stimuli. These results suggest that repeated exposure to the same sensory experience could induce long-term circuitry modifications via 'Hebbian' STDP plasticity.

A new approach for determining phase response curves reveals that Purkinje cells can act as perfect integrators.

Cerebellar Purkinje cells display complex intrinsic dynamics. They fire spontaneously, exhibit bistability, and via mutual network interactions are involved in the generation of high frequency oscillations and travelling waves of activity. To probe the dynamical properties of Purkinje cells we measured their phase response curves (PRCs). PRCs quantify the change in spike phase caused by a stimulus as a function of its temporal position within the interspike interval, and are widely used to predict neuronal responses to more complex stimulus patterns. Significant variability in the interspike interval during spontaneous firing can lead to PRCs with a low signal-to-noise ratio, requiring averaging over thousands of trials. We show using electrophysiological experiments and simulations that the PRC calculated in the traditional way by sampling the interspike interval with brief current pulses is biased. We introduce a corrected approach for calculating PRCs which eliminates this bias. Using our new approach, we show that Purkinje cell PRCs change qualitatively depending on the firing frequency of the cell. At high firing rates, Purkinje cells exhibit single-peaked, or monophasic PRCs. Surprisingly, at low firing rates, Purkinje cell PRCs are largely independent of phase, resembling PRCs of ideal non-leaky integrate-and-fire neurons. These results indicate that Purkinje cells can act as perfect integrators at low firing rates, and that the integration mode of Purkinje cells depends on their firing rate.