On the Contraction of Excitable Systems
Alessandro Cecconi, Michelangelo Bin, Lorenzo Marconi, Rodolphe Sepulchre
TL;DR
The paper analyzes contraction in conductance-based excitable systems to explain reliable spike timing. It proves incremental exponential stability of the unforced Hodgkin–Huxley flow on a compact forward-invariant set and shows contraction persists under impulsive synaptic inputs subject to an average dwell-time or periodicity condition; at high input rates, a tonic, noncontractive regime emerges due to near-constant conductance. By pairing the continuous flow with a hysteretic event detector, the authors show spike times become robust across trials when contraction holds, while dense driving can erase this reliability. Numerical experiments illustrate both regimes, linking spike-timing reliability to contraction and highlighting when rate coding becomes the appropriate description. The work provides a testable framework for when precise spike timing constitutes a faithful information carrier versus when it is subsumed by firing rate, with implications for neuromorphic control and interpretation of neural codes.
Abstract
We analyze contraction in conductance-based excitable systems and link it to reliable spike timing. For a Hodgkin-Huxley neuron with synaptic input, we prove the unforced dynamics is incrementally exponentially stable on a compact physiological set. With impulsive inputs, contraction persists under an average dwell-time condition, and for periodic spike trains we derive an explicit lower bound on the inter-impulse period. In the high-rate limit the synapse is effectively held open, the conductance is nearly constant, and self-sustained limit-cycle oscillations can arise, so contraction no longer holds. This continuous-time view explains when spike times extracted by an event detector remain robust across trials, and simulations confirm both regimes.
