The influence of hyperpolarization-activated cation current on conduction delay and failure of action potentials along axon related to abnormal functions.

Conduction delay and failure behaviors of action potentials with a high frequency along nerve fiber are related to the abnormal functions. For instance, upregulation of a hyperpolarization-activated cation current ( ) is identified to reduce the conduction delay to recover the temporal encoding, and downregulation of the current to enhance the conduction failure rate to ease the pain sensation, with the dynamic mechanisms remaining unclear. In the present paper, the dynamic mechanism is obtained in a chain network model with coupling strength ( ) and action potentials induced by periodic stimulations with a period ( ). At first, as the action potentials exhibit a high frequency corresponding to a short and the network has a small , i.e., a short and unrecovered afterpotential and a small coupling current, the conduction delay is reproduced. The conduction failure is reproduced for shorter and smaller than those of the conduction delay, presenting a direct relationship between the two behaviors. Then, the conduction delay and failure are explained with the response time and current threshold of an action potential evoked from the unrecovered afterpotential. The prolonged response time for short and small presents the cause for the conduction delay, and the enhanced threshold for shorter and smaller presents the cause for the conduction failure. Furthermore, reduction of the delay and enhancement of the failure rate respectively induced by upregulation and downregulation of the current are reproduced and explained. The positive current induces Hopf bifurcation advanced and resting membrane potential elevated. Then, upregulation and downregulation of the current induce the afterpotential elevated to shorten the response time and reduced to enhance the threshold, respectively. The results present nonlinear dynamics for the non-faithful conduction behaviors and dynamical mechanism for the modulation effect of the current on the conduction delay and failure related to encoding and pain.