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On the role of arkypallidal and prototypical neurons for phase transitions in the external pallidum

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Gast,  Richard       
Methods and Development Group Brain Networks, MPI for Human Cognitive and Brain Sciences, Max Planck Society;
Methods and Development Group Nuclear Magnetic Resonance, MPI for Human Cognitive and Brain Sciences, Max Planck Society;

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Gong,  Ruxue
Methods and Development Group Brain Networks, MPI for Human Cognitive and Brain Sciences, Max Planck Society;

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Schmidt,  Helmut       
Methods and Development Group Brain Networks, MPI for Human Cognitive and Brain Sciences, Max Planck Society;

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Knösche,  Thomas R.       
Methods and Development Group Brain Networks, MPI for Human Cognitive and Brain Sciences, Max Planck Society;

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Citation

Gast, R., Gong, R., Schmidt, H., Meijer, H. G., & Knösche, T. R. (2021). On the role of arkypallidal and prototypical neurons for phase transitions in the external pallidum. bioRxiv. doi:10.1101/2021.01.06.425526.


Cite as: https://hdl.handle.net/21.11116/0000-000B-053D-C
Abstract
The external pallidum (GPe) plays a central role for basal ganglia functions and dynamics and, consequently, has been included in most computational studies of the basal ganglia. These studies considered the GPe as a homogeneous neural population. However, experimental studies have shown that the GPe contains at least two distinct cell types (prototypical and arkypallidal cells). In this work, we provide in silico insight into how pallidal heterogeneity modulates dynamic regimes inside the GPe and how they affect the GPe response to oscillatory input.

We derive a mean-field model of the GPe system from a microscopic spiking neural network of recurrently coupled prototypical and arkypallidal neurons. Using bifurcation analysis, we examine the influence of the intra-pallidal connectivity on the GPe dynamics. We find that under healthy conditions, the inhibitory coupling determines whether the GPe is close to either a bi-stable or an oscillatory regime. Furthermore, we show that oscillatory input to the GPe, arriving from subthalamic nucleus or striatum, leads to characteristic patterns of cross-frequency coupling observed at the GPe. Based on these findings, we propose two different hypotheses of how dopamine depletion at the GPe may lead to phase-amplitude coupling between the parkinsonian beta rhythm and a GPe-intrinsic gamma rhythm. Finally, we show that these findings generalize to realistic spiking neural networks of sparsely coupled type-I excitable GPe neurons.