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A multiple timescales approach to bridging spiking- and population-level dynamics
Youngmin Park1, G Bard Ermentrout1
1Department of Mathematics, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, USA.
Chaos (Woodbury, N.Y.)
|September 6, 2018
Summary
This study predicts neural population synchronization from slow synaptic dynamics. The novel theory accurately forecasts phase drift and locking in complex neural networks.
Area of Science:
- Computational Neuroscience
- Theoretical Neuroscience
- Mathematical Biology
Background:
- Bridging spiking-level dynamics and macroscopic quantities in neural populations is crucial.
- Existing methods like the Ott-Antonsen ansatz excel for large, asynchronously firing populations.
- Focus is shifting to understand populations with varying synchronous dynamics.
Purpose of the Study:
- To develop a converse approach predicting synchronization properties of finite neural populations from mean-field dynamics of slow synapses.
- To apply averaging theory and the method of multiple timescales to analyze heterogeneous neural networks.
- To validate the theory using diverse neural models and network configurations.
Main Methods:
- Utilizing averaging theory and the method of multiple timescales for slow synapse dynamics.
- Developing a theory for two heterogeneous populations of excitatory and inhibitory oscillators (n-dimensional and m-dimensional).
- Applying the theory to networks of theta neurons and Traub/Wang-Buzsáki models.
Main Results:
- Accurate prediction of phase drift and phase locking in finite neural populations.
- Demonstrated efficacy across different neural models (theta, Traub, Wang-Buzsáki) and network topologies.
- Validation even when slow synapses exhibit non-trivial mean-field dynamics.
Conclusions:
- The developed theory provides a robust framework for predicting neural synchronization from slow synaptic inputs.
- This approach extends understanding beyond large, asynchronous populations to finite, synchronous networks.
- The findings have implications for modeling complex brain dynamics and neural circuit behavior.
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