Excitatory and inhibitory synaptic coupling can have counter-intuitive effects on the synchronization of neuronal firing. While it might appear that excitatory coupling would lead to synchronization, we show that frequently inhibition rather than excitation synchronizes firing. We study two identical neurons described by integrate-and-fire models, general phase-coupled models or the Hodgkin-Huxley model with mutual, non-instantaneous excitatory or inhibitory synapses between them. We find that if the rise time of the synapse is longer than the duration of an action potential, inhibition not excitation leads to synchronized firing.
We investigate the interaction of an excitable system with a slow oscillation. Under robust and general assumptions compatible with the more stringent assumptions usually made about excitable systems, we show that such a coupled system can display bursting, i.e. a stable solution in which some variable undergoes rapid oscillations followed by a period of quiescence, with both oscillation and quiescence continually repeated. Under a further weak condition, the bursting is "parabolic", i.e. the local frequency of the fast oscillation increases and then decreases within a burst. The technique in this paper involves nonlinear changes of coordinates which transform the equations into ones which are closely related to Hill's equation.
Neuronal activity in a two-dimensional net is analyzed in the neighborhood of an instability. Bifurcation theory and group theory are used to demonstrate the existence of a variety of doubly-periodic patterns, hexagons, rolls, etc., as solutions to the field equations for the net activity. It is suggested that these simple geometric patterns are the cortical concomitants of the "form constants" seen during visual hallucinosis.
Abstract. We consider traveling front and pulse solutions to a system of integro-differential equations used to describe the activity of synaptically coupled neuronal networks in a single spatial dimension. Our first goal is to establish a series of direct links between the abstract nature of the equations and their interpretation in terms of experimental findings in the cortex and other brain regions. This is accomplished first by presenting a biophysically motivated derivation of the system and then by establishing a framework for comparison between numerical and experimental measures of activity propagation speed. Our second goal is to establish the existence of traveling pulse solutions using more rigorous methods. Two techniques are presented. The first, a shooting argument, reduces the problem from finding a specific solution to an integro-differential equation system to finding any solution to an ODE system. The second, a singular perturbation argument, provides a construction of traveling pulse solutions under more general conditions.
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