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Inverse stochastic resonance induced by ion channel noise
BMC Neuroscience volume 13, Article number: P181 (2012)
Recent work has considered the inhibitory effects of noise on neuronal activity, particularly on rhythmic firing. For example, Paydarfar et al.  studied the influence of noise on neuronal pacemakers in an in vitro preparation of the squid giant axon, and found that small noisy currents induce an on-off switching behavior between two nearby regimes: repetitive firing and quiescence. They also showed that the timings of on-off switching of the pacemaker depend on the intensity and spectral properties of noisy current. Tuckwell et al. [2, 3] further investigated the inhibitory effect of noise in a single Hodgkin-Huxley neuron. These authors show that in a model neuron subject to stochastic external additive noise, the average firing rate exhibits a minimum as the noise amplitude is varied. The authors called this phenomenon Inverse Stochastic Resonance (ISR), in contrast to the well-known phenomenon of stochastic resonance.
In these modelling studies [2, 3], noise was incorporated by adding an external noisy current. Here, we consider the ISR phenomenon in the Hodgkin-Huxley neuron with a more biophysically realistic model of noise: that resulting from the stochastic nature of voltage-gated ion channels embedded in neuronal membranes. The intensity of channel noise is related to the total number of channels for fixed channel density, i.e. when the number of ion channels (or the cell size) is small, the stochasticity of channels imparts strong noise intensity to the neuron’s dynamics. Our results show that the ISR phenomenon is also present in the case of ion channel noise. We clarify the mechanism that underlies ISR and show that the most surprising feature – the increase in average firing rate as the noise decreases (membrane area increases) – is a consequence of the dynamical structure of the model and the averaging procedure (Figure 1). We also discuss the relative contributions of the different channel subunits to transitions from the spiking to the rest state, and vice versa, in the noisy case.
Paydarfar D, Forger DB, Clay JR: Noisy inputs and the induction of on–off switching behavior in a neuronal pacemaker. J Neurophysiol. 2006, 96: 3338-3348. 10.1152/jn.00486.2006.
Tuckwell HC, Jost J, Gutkin BS: Inhibition and modulation of rhythmic neuronal spiking by noise. Phys Rev Lett. 2009, 80: 031907-8.
Tuckwell HC, Jost J: Weak noise in neurons may powerfully inhibit the generation of repetitive spiking but not its propagation. Plos Comput Biol. 1000, 6: e794-13.