Facilitation, Biophysical Models
نویسنده
چکیده
Facilitation is a temporary increase in postsynaptic response to a presynaptic action potential or depolarization induced by a preceding presynaptic depolarization. It is distinguished from longer-term components of activity-dependent synaptic enhancement by its low activation threshold (a pair of action potentials is often sufficient, hence the term paired-pulse facilitation) and short persistence time: facilitated response decays back to initial amplitude within less than a second after the stimulus train. Facilitation is very common in central and peripheral synapses of both vertebrate and invertebrate nervous systems; it is readily observed under conditions of low initial vesicle release probability, but is often occluded by synaptic depression when the initial vesicle release probability is sufficiently high. Biophysical models of facilitation go beyond a simple phenomenological description and often combine a model for presynaptic Ca2+ dynamics with a model of Ca2+ binding to exocytosis sites that trigger vesicle fusion. Detailed Description
منابع مشابه
Biophysical properties of presynaptic short-term plasticity in hippocampal neurons: insights from electrophysiology, imaging and mechanistic models
Hippocampal neurons show different types of short-term plasticity (STP). Some exhibit facilitation of their synaptic responses and others depression. In this review we discuss presynaptic biophysical properties behind heterogeneity in STP in hippocampal neurons such as alterations in vesicle priming and docking, fusion, neurotransmitter filling and vesicle replenishment. We look into what types...
متن کاملEffects of mobile buffers on facilitation: experimental and computational studies.
Facilitation is an important form of short-term plasticity that occurs in most synapses. At crayfish neuromuscular junctions, basal transmission and facilitation were significantly reduced after presynaptic introduction of "fast" high-affinity calcium buffers, and the decay of facilitation was accelerated. The existence of residual calcium during facilitation was also demonstrated. Computationa...
متن کاملTime course of transmitter release calculated from simulations of a calcium diffusion model.
A three-dimensional presynaptic calcium diffusion model developed to account for characteristics of transmitter release was modified to provide for binding of calcium to a receptor and subsequent triggering of exocytosis. When low affinity (20 microM) and rapid kinetics were assumed for the calcium receptor triggering exocytosis, and stimulus parameters were selected to match those of experimen...
متن کاملPresynaptic calcium diffusion from various arrays of single channels. Implications for transmitter release and synaptic facilitation.
A one-dimensional model of presynaptic calcium diffusion away from the membrane, with cytoplasmic binding, extrusion by a surface pump, and influx during action potentials, can account for the rapid decay of phasic transmitter release and the slower decay of synaptic facilitation following one spike, as well as the very slow decline in total free calcium observed experimentally. However, simula...
متن کاملThe calcium hypothesis and modulation of transmitter release by hyperpolarizing pulses.
Small presynaptic conditioning hyperpolarizing pulses reduce transmitter release to a depolarizing stimulus by a substantial amount, with little effect on release by a subsequent depolarization. This result, obtained at neuromuscular junctions and the squid giant synapse, has been offered as a disproof of the calcium hypothesis of transmitter release or the residual calcium hypothesis of synapt...
متن کامل