Dynamics of excitability over extended timescales in cultured cortical neurons.

Although neuronal excitability is well understood and accurately modeled over timescales of up to hundreds of milliseconds, it is currently unclear whether extrapolating from this limited duration to longer behaviorally relevant timescales is appropriate. Here we used an extracellular recording and stimulation paradigm that extends the duration of single-neuron electrophysiological experiments, exposing the dynamics of excitability in individual cultured cortical neurons over timescales hitherto inaccessible. We show that the long-term neuronal excitability dynamics is unstable and dominated by critical fluctuations, intermittency, scale-invariant rate statistics, and long memory. These intrinsic dynamics bound the firing rate over extended timescales, contrasting observed short-term neuronal response to stimulation onset. Furthermore, the activity of a neuron over extended timescales shows transitions between quasi-stable modes, each characterized by a typical response pattern. Like in the case of rate statistics, the short-term onset response pattern that often serves to functionally define a given neuron is not indicative of its long-term ongoing response. These observations question the validity of describing neuronal excitability based on temporally restricted electrophysiological data, calling for in-depth exploration of activity over wider temporal scales. Such extended experiments will probably entail a different kind of neuronal models, accounting for the unbounded range, from milliseconds up.