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Nolte, M.

Publications and source records attributed to Nolte, M..

2 recordsLinked to original sources

Impact of higher-order network structure on emergent cortical activity

Synaptic connectivity between neocortical neurons is highly structured. The network structure of synaptic connectivity includes first-order properties that can be described by pairwise statistics, such as strengths of connections between different neuron types and distance-dependent connectivity, and higher-order properties, such as an abundance of cliques of all-to-all connected neurons. The relative impact of first- and higher-order structure on emergent cortical network activity is unknown. Here, we compare network structure and emergent activity in two neocortical microcircuit models with different synaptic connectivity. Both models have a similar first-order structure, but only one model includes higher-order structure arising from morphological diversity within neuronal types. We find that such morphological diversity leads to more heterogeneous degree distributions, increases the number of cliques, and contributes to a small-world topology. The increase in higher-order network structure is accompanied by more nuanced changes in neuronal firing patterns, such as an increased dependence of pairwise correlations on the positions of neurons in cliques. Our study shows that circuit models with very similar first-order structure of synaptic connectivity can have a drastically different higher-order network structure, and suggests that the higher-order structure imposed by morphological diversity within neuronal types has an impact on emergent cortical activity.

neuroscience↗

Cortical Reliability Amid Noise and Chaos

Typical responses of cortical neurons to identical sensory stimuli are highly variable. It has thus been proposed that the cortex primarily uses a rate code. However, other studies have argued for spike-time coding under certain conditions. The potential role of spike-time coding is constrained by the intrinsic variability of cortical circuits, which remains largely unexplored. Here, we quantified this intrinsic variability using a biophysical model of rat neocortical microcircuitry with biologically realistic noise sources. We found that stochastic neurotransmitter release is a critical component of this variability, which, amplified by recurrent connectivity, causes rapid chaotic divergence with a time constant on the order of 10-20 milliseconds. Surprisingly, weak thalamocortical stimuli can transiently overcome the chaos, and induce reliable spike times with millisecond precision. We show that this effect relies on recurrent cortical connectivity, and is not a simple effect of feed-forward thalamocortical input. We conclude that recurrent cortical architecture supports millisecond spike-time reliability amid noise and chaotic network dynamics, resolving a long-standing debate.

neuroscience↗