Sleep spindles in primates: Modeling the effects of distinct laminar thalamocortical connectivity in core, matrix, and reticular thalamic circuits

Author:

Yazdanbakhsh Arash123ORCID,Barbas Helen2345,Zikopoulos Basilis2356ORCID

Affiliation:

1. Computational Neuroscience and Vision Lab, Department of Psychological and Brain Sciences, Boston University, Boston, MA, USA

2. Graduate Program for Neuroscience, Boston University, Boston, MA, USA

3. Center for Systems Neuroscience, Boston, MA, USA

4. Neural Systems Laboratory, Program in Human Physiology, Department of Health Sciences, College of Health and Rehabilitation Sciences (Sargent College), Boston University, Boston, MA, USA

5. Department of Anatomy and Neurobiology, Boston University School of Medicine, Boston University, Boston, MA, USA

6. Human Systems Neuroscience Laboratory, Program in Human Physiology, Department of Health Sciences, College of Health and Rehabilitation Sciences (Sargent College), Boston University, Boston, MA, USA

Abstract

Abstract Sleep spindles are associated with the beginning of deep sleep and memory consolidation and are disrupted in schizophrenia and autism. In primates, distinct core and matrix thalamocortical (TC) circuits regulate sleep spindle activity through communications that are filtered by the inhibitory thalamic reticular nucleus (TRN); however, little is known about typical TC network interactions and the mechanisms that are disrupted in brain disorders. We developed a primate-specific, circuit-based TC computational model with distinct core and matrix loops that can simulate sleep spindles. We implemented novel multilevel cortical and thalamic mixing, and included local thalamic inhibitory interneurons, and direct layer 5 projections of variable density to TRN and thalamus to investigate the functional consequences of different ratios of core and matrix node connectivity contribution to spindle dynamics. Our simulations showed that spindle power in primates can be modulated based on the level of cortical feedback, thalamic inhibition, and engagement of model core versus matrix, with the latter having a greater role in spindle dynamics. The study of the distinct spatial and temporal dynamics of core-, matrix-, and mix-generated sleep spindles establishes a framework to study disruption of TC circuit balance underlying deficits in sleep and attentional gating seen in autism and schizophrenia.

Funder

National Institute of Mental Health

Publisher

MIT Press

Subject

Applied Mathematics,Artificial Intelligence,Computer Science Applications,General Neuroscience

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