Abstract
Synapses are critical actors of neuronal transmission as they form the basis of chemical communication between neurons. Accurate computational models of synaptic dynamics may prove important in elucidating emergent properties across hierarchical scales. Yet, in large-scale neuronal network simulations, synapses are often modeled as highly simplified linear exponential functions due to their small computational footprint. However, these models cannot capture the complex non-linear dynamics that biological synapses exhibit and thus, are insufficient in representing synaptic behavior accurately. Existing detailed mechanistic synapse models can replicate these non-linear dynamics by modeling the underlying kinetics of biological synapses, but their high complexity prevents them from being a suitable option in large-scale models due to long simulation times. This motivates the development of more parsimonious models that can capture the complex non-linear dynamics of synapses accurately while maintaining a minimal computational cost. We propose a look-up table approach that stores precomputed values thereby circumventing most computations at runtime and enabling extremely fast simulations for glutamatergic receptors AMPAr and NMDAr. Our results demonstrate that this methodology is capable of replicating the dynamics of biological synapses as accurately as the mechanistic synapse models while offering up to a 56-fold increase in speed. This powerful approach allows for multi-scale neuronal networks to be simulated at large scales, enabling the investigation of how low-level synaptic activity may lead to changes in high-level phenomena, such as memory and learning.
Highlights
In modern neuroscience, computational modeling has become a pivotal part of research as it allows for the investigation of underlying physiological neural mechanisms that are often too difficult to test experimentally on live tissue
The outputs of the validation datasets were the responses given by the AMPAr or NMDAr kinetic models implemented in NEURON
The exponential synapse models performed the worst in every case with normalized root mean square error (NRMSE) values ranging from 10 to 27% in AMPAr and 42 to 65% in NMDAr due to their inability to capture any degree of non-linearity while the look-up table synapse (LUTsyn) model maintained NRMSE values ranging from 6 to 11% in AMPAr and 9 to 12% in NMDAr
Summary
Computational modeling has become a pivotal part of research as it allows for the investigation of underlying physiological neural mechanisms that are often too difficult to test experimentally on live tissue. Multi-scale and large-scale models of the nervous system aim to replicate and integrate complex dynamics across multiple hierarchies (e.g., molecular, synaptic, Look-Up Table Synapse Model single neuron, neuronal network) within large networks of neurons Such models have the potential to further our understanding of how low-level mechanisms (such as biomolecular interactions) might affect high-level outcomes, such as cognition (Micheli et al, 2021). Multi- and large-scale models of entire neural subsystems that are anatomically detailed with connectivity or that consider cell morphology closely tend to require entire clusters of computing nodes to simulate (Izhikevich and Edelman, 2008; Yu et al, 2013) These multi-scale models have potential for in silico experimentation of neurological perturbations either due to specific pathologies, electrical stimulation (electrotherapy), or the influence of exogenous compounds (i.e., drugs), thereby constituting a useful platform for the discovery and development of novel therapeutics. For multi- and large-scale models to attain such predictive power, they must provide a sufficiently accurate representation of the underlying neuronal processes, making it necessary to depict their constituents, at all levels, with biological accuracy
Published Version
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