Corticopetal acetylcholine (ACh) is released transiently from the nucleus basalis of Meynert (NBM) into the cortical layers and is associated with top-down attention. Recent experimental data suggest that this release of ACh disinhibits layer 2/3 pyramidal neurons (PYRs) via muscarinic presynaptic effects on inhibitory synapses. Together with other possible presynaptic cholinergic effects on excitatory synapses, this may result in dynamic and temporal modifications of synapses associated with top-down attention. However, the system-level consequences and cognitive relevance of such disinhibitions are poorly understood. Herein, we propose a theoretical possibility that such transient modifications of connectivity associated with ACh release, in addition to top-down glutamatergic input, may provide a neural mechanism for the temporal reactivation of attractors as neural correlates of memories. With baseline levels of ACh, the brain returns to quasi-attractor states, exhibiting transitive dynamics between several intrinsic internal states. This suggests that top-down attention may cause the attention-induced deformations between two types of attractor landscapes: the quasi-attractor landscape (Q-landscape, present under low-ACh, non-attentional conditions) and the attractor landscape (A-landscape, present under high-ACh, top-down attentional conditions). We present a conceptual computational model based on experimental knowledge of the structure of PYRs and interneurons (INs) in cortical layers 1 and 2/3 and discuss the possible physiological implications of our results.
The globally connected active rotators with excitatory and inhibitory connections are analyzed using the nonlinear Fokker-Planck equation. The bifurcation diagram of the system is obtained numerically, and both periodic solutions and chaotic solutions are found. By observing the interspike interval, the coefficient of variance, and the correlation coefficient of the system, the relationship of our model to the biological data is discussed.
Nonlinear dynamics of coupled FitzHugh-Nagumo neurons subject to independent noise is analyzed. A kind of self-sustained global oscillation with almost synchronous firing is generated by array-enhanced coherence resonance. Further, forced dynamics of the self-sustained global oscillation stimulated by sinusoidal input is analyzed and classified as synchronized, quasiperiodic, and chaotic responses just like the forced oscillations in nerve membranes observed by in vitro experiments with squid giant axons. Possible physiological importance of such forced oscillations is also discussed.
The synchronous firing of neurons in a pulse coupled neural network composed of excitatory and inhibitory neurons is analyzed. The neurons are connected by both chemical synapses and electrical synapses among the inhibitory neurons. By introducing electrical synapses, periodically synchronized firing as well as chaotically synchronized firing is widely observed. Moreover, we find stochastic synchrony where the ensemble-averaged dynamics shows synchronization in the network but each neuron has a low firing rate and the firing of the neurons seems to be stochastic. Stochastic synchrony of chaos corresponding to a chaotic attractor is also found.
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