A simple circuit is described that functions as an analog memory whose state and dynamics are directly controlled by pulsatile inputs. The circuit has been incorporated into a silicon neuron with a spatially extensive dendritic tree as a means of controlling the spike firing threshold of an integrate-and-fire soma. Spiking activity generated by the neuron itself and by other units in a network can thereby regulate the neuron's excitability over time periods ranging from milliseconds to many minutes. Experimental results are presented showing applications to temporal edge sharpening, bistable behavior, and a network that learns in the manner of classical conditioning.

A dendritic tree, as part of a silicon neuromorph, was modeled in VLSI as a multibranched, passive cable structure with multiple synaptic sites that either depolarize or hyperpolarize local “membrane patches,” thereby raising or lowering the probability of spike generation of an integrate-and-fire “soma.” As expected from previous theoretical analyses, contemporaneous synaptic activation at widely separated sites on the artificial tree resulted in near-linear summation, as did neighboring excitatory and inhibitory activations. Activation of synapses of the same type close in time and space produced local saturation of potential, resulting in spike train processing capabilities not possible with linear summation alone. The resulting sublinear synaptic summation, as well as being physiologically plausible, is sufficient for a variety of spike train processing functions. With the appropriate arrangement of synaptic inputs on its dendritic tree, a neuromorph was shown to discriminate input pulse intervals and patterns, pulse train frequencies, and detect correlation between input trains.