Neurons in the central nervous system are affected by complex and noisy signals due to fluctuations in their cellular environment and in the inputs they receive from many other cells 1,2. Such noise usually increases the probability that a neuron wil
l send out a signal to its target cells 2-5. In stochastic resonance, which occurs in many physical and biological systems, an optimal response is found at a particular noise amplitude 6-9. We have found that in a classical neuronal model the opposite can occur - that noise can subdue or turn off repetitive neuronal activity in both single cells and networks of cells. Recent experiments on regularly firing neurons with noisy inputs confirm these predictions 10,11. Surprisingly, we find that in some cases there is a noise level at which the response is a minimum, a phenomenon which is called inverse stochastic resonance. Suppression of rhythmic behavior by noise and inverse stochastic resonance are predicted to occur not only in neuronal systems but more generally in diverse nonlinear dynamical systems where a stable limit cycle is attainable from a stable rest state.
We examine the effects of stochastic input currents on the firing behavior of two excitable neurons coupled with fast excitatory synapses. In such cells (models), typified by the quadratic integrate and fire model, mutual synaptic coupling can cause
sustained firing or oscillatory behavior which is necessarily antiphase. Additive Gaussian white noise can transiently terminate the oscillations, hence destroying the stable limit cycle. Further application of the noise may return the system to spiking activity. In a particular noise range, the transition times between the oscillating and the resting state are strongly asymmetric. We numerically investigate an approximate basin of attraction, A, of the periodic orbit and use Markov process theory to explain the firing behavior in terms of the probability of escape of trajectories from A
