Topic: synaptic efficacy

Recurrent neural networks, a ubiquitous construct in machine intelligence, have become a powerful hypothesis-generating tool in theoretical neuroscience. Such networks can be used to examine potential circuit mechanisms associated with a variety of cognitive functions. Here, we use recurrent networks to engage a new theoretical question: the potential role of astrocytes in neural computation. Astrocytes are highly abundant cells in the cortex that are capable of modulating many facets of neural dynamics, including excitability, synaptic efficacy and plasticity. However, despite this modulatory

A signature feature of cortical circuits is the irregularity of neuronal firing, which manifests itself in the high temporal variability of spiking and the broad distribution of rates. Theoretical works have shown that this feature emerges dynamically in network models if coupling between cells is strong, i.e. if the mean number of synapses per neuron K is large and synaptic efficacy is of order 1/\sqrt{K}. However, the degree to which these models capture the mechanisms underlying neuronal firing in cortical circuits is not fully understood. Results have been derived using neuron models with

It is widely believed that storing and maintaining memories on long-time scales depends on modifying synapses in the brain in an activity-dependent way. Classical studies of learning and memory in neural networks model synaptic efficacy as a continuous or discrete scalar value [1–3]. Theoretical work has shown such models have a reasonably large capacity, especially in the biologically relevant sparse coding limit [4]. However, multiple recent results suggest an intermediate scenario in which synaptic efficacy can be described by a continuous variable, but whose distribution is peaked around a

Activity dependent synaptic plasticity is considered to be a primary mechanism underlying learning and memory. Yet it is unclear whether plasticity rules such as STDP measured in vitro apply in vivo. Network models with STDP predict that activity patterns (e.g., place-cell spatial selectivity) should change much faster than observed experimentally. We address this gap by investigating a nonlinear calcium-based plasticity rule fit to experiments done in physiological conditions. In this model, LTP and LTD result from intracellular calcium transients arising almost exclusively from synchronous c