We have investigated the role that different connectivity regimes play in the dynamics of a network of Hodgkin-Huxley neurons by computer simulations. The different connectivity topologies exhibit the following features: random topologies give rise to fast system response yet are unable to produce coherent oscillations in the average activity of the network; on the other hand, regular topologies give rise to coherent oscillations, but in a temporal scale that is not in accordance with fast signal processing. Finally, small-world topologies, which fall between random and regular ones, take advantage of the best features of both, giving rise to fast system response with coherent oscillations.

Following studies of olfactory processing in insects and fish, we investigate neural networks whose dynamics in phase space is represented by orbits near the heteroclinic connections between saddle regions (fixed points or limit cycles). These networks encode input information as trajectories along the heteroclinic connections. If there are $N$ neurons in the network, the capacity is approximately $e(N-1\mathrm{})!$, i.e., much larger than that of most traditional network structures. We show that a small winnerless competition network composed of FitzHugh-Nagumo spiking neurons efficiently transforms input information into a spatiotemporal output.

The idea that cognitive activity can be understood using nonlinear dynamics has been intensively discussed at length for the last 15 years. One of the popular points of view is that metastable states play a key role in the execution of cognitive functions. Experimental and modeling studies suggest that most of these functions are the result of transient activity of large-scale brain networks in the presence of noise. Such transients may consist of a sequential switching between different metastable cognitive states. The main problem faced when using dynamical theory to describe transient cognitive processes is the fundamental contradiction between reproducibility and flexibility of transient behavior. In this paper, we propose a theoretical description of transient cognitive dynamics based on the interaction of functionally dependent metastable cognitive states. The mathematical image of such transient activity is a stable heteroclinic channel, i.e., a set of trajectories in the vicinity of a heteroclinic skeleton that consists of saddles and unstable separatrices that connect their surroundings. We suggest a basic mathematical model, a strongly dissipative dynamical system, and formulate the conditions for the robustness and reproducibility of cognitive transients that satisfy the competing requirements for stability and flexibility. Based on this approach, we describe here an effective solution for the problem of sequential decision making, represented as a fixed time game: a player takes sequential actions in a changing noisy environment so as to maximize a cumulative reward. As we predict and verify in computer simulations, noise plays an important role in optimizing the gain. The modeling of the temporal structure of cognitive processes is a key step for understanding cognition. Cognitive functions such as sequential learning, short-term memory, and decision making in a changing environment cannot be understood using only the traditional view based on classical concepts of nonlinear dynamics, which describe static or rhythmic brain activity. The execution of many cognitive functions is a transient dynamical process. Any dynamical mechanism underlying cognitive processes has to be reproducible from experiment to experiment in similar environmental conditions and, at the same time, it has to be sensitive to changing internal and external information. We propose here a new dynamical object that can represent robust and reproducible transient brain dynamics. We also propose a new class of models for the analysis of transient dynamics that can be applied for sequential decision making.

We report experimental studies of synchronization phenomena in a pair of biological neurons that interact through naturally occurring, electrical coupling. When these neurons generate irregular bursts of spikes, the natural coupling synchronizes slow oscillations of membrane potential, but not the fast spikes. By adding artificial electrical coupling we studied transitions between synchrony and asynchrony in both slow oscillations and fast spikes. We discuss the dynamics of bursting and synchronization in living neurons with distributed functional morphology.