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Published on: August 2, 2017
Spatially targeted inhibitory rhythms differentially affect neuronal integration
Drew B Headley1, Benjamin Latimer2, Adin Aberbach2
1Center for Molecular and Behavioral Neuroscience, Rutgers University - Newark, Newark, United States.
Inhibitory rhythms and their location on pyramidal neurons differentially regulate neuronal integration. Gamma rhythms at the soma impact action potentials, while beta rhythms in dendrites affect dendritic spikes and their timing.
Area of Science:
- Neuroscience
- Computational Neuroscience
- Cellular Electrophysiology
Background:
- Pyramidal neurons integrate inputs via recurrent networks involving inhibitory interneurons.
- Inhibitory interneurons differ in their synaptic targets (perisomatic vs. dendritic) and rhythmic firing patterns (beta and gamma frequencies).
- The interplay between inhibitory rhythmicity and spatial targeting influences neuronal integration.
Purpose of the Study:
- To investigate how rhythmic perisomatic and distal dendritic inhibition impact integration in a layer 5 pyramidal neuron model.
- To determine the location- and rhythm-dependent effects of inhibition on neuronal excitability and spike coupling.
Main Methods:
- Computational modeling of a layer 5 pyramidal neuron with realistic dendritic morphology.
- Incorporation of active dendritic properties supporting Na+, NMDA, and Ca2+ spikes.
- Simulation of rhythmic perisomatic and distal dendritic inhibition at beta and gamma frequencies.
Main Results:
- Inhibition regulated the coupling between dendritic spikes and action potentials in a location- and rhythm-dependent manner.
- Perisomatic inhibition primarily controlled action potential generation, while distal dendritic inhibition affected dendritic spike incidence and temporal coupling.
- Gamma-frequency perisomatic inhibition and beta-frequency distal dendritic inhibition were most effective.
- Beta rhythms modulated distal input responsiveness phase-dependently, while gamma rhythms modulated proximal input responsiveness.
Conclusions:
- Location and rhythm of inhibition critically shape neuronal integration.
- Findings suggest a functional basis for the association of parvalbumin interneurons with gamma rhythms and somatostatin interneurons with beta rhythms.
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