Back to Search Start Over

Pathological cell assembly dynamics in a striatal MSN network model.

Authors :
Correa A
Ponzi A
Calderón VM
Migliore R
Source :
Frontiers in computational neuroscience [Front Comput Neurosci] 2024 Jun 06; Vol. 18, pp. 1410335. Date of Electronic Publication: 2024 Jun 06 (Print Publication: 2024).
Publication Year :
2024

Abstract

Under normal conditions the principal cells of the striatum, medium spiny neurons (MSNs), show structured cell assembly activity patterns which alternate sequentially over exceedingly long timescales of many minutes. It is important to understand this activity since it is characteristically disrupted in multiple pathologies, such as Parkinson's disease and dyskinesia, and thought to be caused by alterations in the MSN to MSN lateral inhibitory connections and in the strength and distribution of cortical excitation to MSNs. To understand how these long timescales arise we extended a previous network model of MSN cells to include synapses with short-term plasticity, with parameters taken from a recent detailed striatal connectome study. We first confirmed the presence of sequentially switching cell clusters using the non-linear dimensionality reduction technique, Uniform Manifold Approximation and Projection (UMAP). We found that the network could generate non-stationary activity patterns varying extremely slowly on the order of minutes under biologically realistic conditions. Next we used Simulation Based Inference (SBI) to train a deep net to map features of the MSN network generated cell assembly activity to MSN network parameters. We used the trained SBI model to estimate MSN network parameters from ex-vivo brain slice calcium imaging data. We found that best fit network parameters were very close to their physiologically observed values. On the other hand network parameters estimated from Parkinsonian, decorticated and dyskinetic ex-vivo slice preparations were different. Our work may provide a pipeline for diagnosis of basal ganglia pathology from spiking data as well as for the design pharmacological treatments.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2024 Correa, Ponzi, Calderón and Migliore.)

Details

Language :
English
ISSN :
1662-5188
Volume :
18
Database :
MEDLINE
Journal :
Frontiers in computational neuroscience
Publication Type :
Academic Journal
Accession number :
38903730
Full Text :
https://doi.org/10.3389/fncom.2024.1410335