ArticlePloS one2010
Mechanisms explaining transitions between tonic and phasic firing in neuronal populations as predicted by a low dimensional firing rate model.
Article in PloS one, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Electroencephalography complexity in resting and task states in adults with attention-deficit/hyperactivity disorder.Brain communications · 2022Article
- Single-layer graphene modulates neuronal communication and augments membrane ion currents.Nature nanotechnology · 2018Article
- Global and local excitation and inhibition shape the dynamics of the cortico-striatal-thalamo-cortical pathway.Scientific reports · 2017Article
- Neuromorphic meets neuromechanics, part II: the role of fusimotor drive.Journal of neural engineering · 2017Article
- NPR-9, a Galanin-Like G-Protein Coupled Receptor, and GLR-1 Regulate Interneuronal Circuitry Underlying Multisensory Integration of Environmental Cues in Caenorhabditis elegans.PLoS genetics · 2016Article
- Reading the Freudian theory of sexual drives from a functional neuroimaging perspective.Frontiers in human neuroscience · 2014Article
- Rapid regulation of depression-related behaviours by control of midbrain dopamine neurons.Nature · 2013Article
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Abstract
Several firing patterns experimentally observed in neural populations have been successfully correlated to animal behavior. Population bursting, hereby regarded as a period of high firing rate followed by a period of quiescence, is typically observed in groups of neurons during behavior. Biophysical membrane-potential models of single cell bursting involve at least three equations. Extending such models to study the collective behavior of neural populations involves thousands of equations and can be very expensive computationally. For this reason, low dimensional population models that capture biophysical aspects of networks are needed. The present paper uses a firing-rate model to study mechanisms that trigger and stop transitions between tonic and phasic population firing. These mechanisms are captured through a two-dimensional system, which can potentially be extended to include interactions between different areas of the nervous system with a small number of equations. The typical behavior of midbrain dopaminergic neurons in the rodent is used as an example to illustrate and interpret our results. The model presented here can be used as a building block to study interactions between networks of neurons. This theoretical approach may help contextualize and understand the factors involved in regulating burst firing in populations and how it may modulate distinct aspects of behavior.
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