The provided code models a graded synapse with first-order binding kinetics, specifically focusing on an excitatory synapse, likely mediated by AMPA-type glutamate receptors. Here is a breakdown of the biological basis that directly relates to the code:
Graded Synapse:
Neurotransmitter Binding Kinetics:
Excitatory Synapse:
e = -70 mV
indicates the reversal potential, suggesting a synapse that is excitatory. Excitatory synapses often involve AMPA receptors that permeate sodium (Na+) and potassium (K+) ions, leading to depolarization of the postsynaptic cell.Voltage-Dependence:
V_pre
) influences the state (s_inf
) of the synapse. The threshold (V_thr
) and slope (V_slope
) parameters define how sensitive neurotransmitter release is to changes in membrane potential, reflecting the synapse's intrinsic properties.Maximal Conductance:
g_max
parameter represents the maximal conductance of the dAMPA (decayed AMPA receptor), akin to the maximal number of receptor channels available for ion passage upon full activation by neurotransmitters.Conductance-Based Synaptic Current:
i
) as a product of conductance (g
) and the driving force (the difference between the postsynaptic membrane potential and the reversal potential), common in excitatory synapse models involving AMPA receptors.Gating Variable (s
): Represents the fraction of open synaptic receptor channels influenced by neurotransmitter binding. Its dynamics are governed by the difference between its steady-state value (s_inf
) and its current value, scaling with the kinetic parameter tau, reflecting synaptic plasticity and desensitization.
Steady-State Activation (s_inf
): This is determined by a hyperbolic tangent function, indicative of a continuous and graded response to presynaptic membrane potential (V_pre
), which directly ties to the nature of graded synaptic transmission.
The model's focus on graded synaptic transmission and voltage-dependent conductance changes mirrors the complexities found in certain neuronal systems, emphasizing the nuanced control of synaptic efficacy beyond traditional all-or-nothing mechanisms.