Abstract

Neuromodulators are endogenous neurochemicals that regulate biophysical and biochemical processes, which control brain function and behaviour, and are often the targets of neuropharmacological drugs. Neuromodulator effects are generally complex partly owing to the involvement of broad innervation, co-release of neuromodulators, complex intra- and extrasynaptic mechanism, existence of multiple receptor subtypes and high interconnectivity within the brain. In this work, we propose an efficient yet sufficiently realistic computational neural modelling framework to study some of these complex behaviours. Specifically, we propose a novel dynamical neural circuit model that integrates the effective neuromodulator-induced currents based on various experimental data (e.g. electrophysiology, neuropharmacology and voltammetry). The model can incorporate multiple interacting brain regions, including neuromodulator sources, simulate efficiently and easily extendable to large-scale brain models, e.g. for neuroimaging purposes. As an example, we model a network of mutually interacting neural populations in the lateral hypothalamus, dorsal raphe nucleus and locus coeruleus, which are major sources of neuromodulator orexin/hypocretin, serotonin and norepinephrine/noradrenaline, respectively, and which play significant roles in regulating many physiological functions. We demonstrate that such a model can provide predictions of systemic drug effects of the popular antidepressants (e.g. reuptake inhibitors), neuromodulator antagonists or their combinations. Finally, we developed user-friendly graphical user interface software for model simulation and visualization for both fundamental sciences and pharmacological studies.

Highlights

  • Neuronal activities, through the firing of action potentials and synaptic transmissions, can be modulated by endogenous neurochemicals called neuromodulators, acting through biophysical and biochemical processes [1,2]

  • For dorsal raphe nucleus (DRN), pLS is changed from 22.08 to 22.97 nM and pS from 0.452 to 0.367. We find that this triple-drug combination can cause a further decrease in the fDRN and fLC, and a substantial reduction in [NE]DRN levels, whereas the rest are not significantly affected by the addition of SB-334867-A

  • We have proposed a new computational modelling framework for incorporating essential biological features of neuromodulation in neural circuits

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Summary

Introduction

Through the firing of action potentials and synaptic transmissions, can be modulated by endogenous neurochemicals called neuromodulators, acting through biophysical and biochemical processes [1,2]. These neuromodulators are released by a distinct population of neurons, and the neuromodulators act on specific receptors which are distributed throughout the brain [3]. In neuropharmacological drug treatment of neurological and neuropsychiatric illnesses, the monoaminergic systems (especially that of serotonin, dopamine and NE) are often targeted [4].

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