| name | isi-adaptive-threshold-neuronal-networks |
| description | First-passage-time analysis of inter-spike interval (ISI) statistics for excitatory-inhibitory (EI) integrate-and-fire neurons with depolarizing and hyperpolarizing adaptive thresholds. Use when studying stochastic neuronal firing, ISI variability, adaptive threshold mechanisms, or EI balance effects on spike-time statistics. |
| metadata | {"arxiv_id":"2607.18428","published":"2026-07-22","authors":["Oliver Gambrell","Abhyudai Singh"],"tags":["neuroscience","spiking-neurons","inter-spike-interval","adaptive-threshold","EI-balance","first-passage-time","stochastic-neuronal-dynamics"]} |
| license | Complete terms in LICENSE.txt |
ISI Statistics in Adaptive-Threshold Neuronal Networks
A first-passage-time methodology for analyzing how depolarizing and hyperpolarizing adaptive thresholds shape the mean and variability of inter-spike intervals in excitatory-inhibitory (EI) integrate-and-fire neurons.
Core Idea
Extend the classical integrate-and-fire model by letting the threshold potential depend on recent presynaptic activity. This captures two biophysical effects:
- Depolarizing adaptive threshold: threshold rises after excitation (spike-frequency adaptation via sodium/calcium-activated potassium channels).
- Hyperpolarizing adaptive threshold: threshold falls after inhibition (post-inhibitory rebound via sodium channel recovery from inactivation).
The framework derives the ISI distribution via first-passage-time (FPT) analysis and quantifies ISI noise with the coefficient of variation (CV).
When to Use
- Modeling spike-time variability in EI circuits.
- Comparing fixed vs. adaptive threshold effects on firing regularity.
- Predicting post-inhibitory rebound spiking.
- Studying how excitatory/inhibitory input balance affects ISI statistics.
Key Findings
- Depolarizing adaptive thresholds increase ISI noise relative to fixed thresholds at the same mean ISI.
- ISI noise can be hypo- or hyper-exponential (CV < 1 or CV > 1) depending on excitatory and inhibitory input rates.
- Hyperpolarizing adaptive thresholds can generate spikes driven purely by inhibition, producing post-inhibitory rebound firing.
- Quantal content (QC) is modeled as binomial random variables, linking synaptic release stochasticity to postsynaptic firing statistics.
Methodology
- Model the postsynaptic neuron as a leaky integrate-and-fire neuron receiving Poisson excitatory and inhibitory inputs.
- Model quantal content of each presynaptic AP as independent binomial random variables with known mean and variance.
- Fix a threshold potential for the baseline case; then extend to adaptive thresholds:
- Depolarizing: threshold increases with membrane depolarization.
- Hyperpolarizing: threshold decreases with membrane hyperpolarization.
- Apply first-passage-time analysis to derive the mean ISI and the coefficient of variation.
- Validate analytical predictions with stochastic simulations across input-rate parameter space.
Implementation Sketch
import numpy as np
Parameter Sensitivities
- High, balanced EI rates maximize ISI noise (CV²) in the fixed-threshold model.
- Depolarizing threshold systematically raises CV for matched mean ISI.
- Hyperpolarizing threshold introduces rebound spikes even when net synaptic drive is inhibitory.
Pitfalls
- Adaptive threshold dynamics must be slow enough relative to the membrane time constant; otherwise the model effectively reverts to a fixed threshold.
- Binomial QC approximation assumes independent vesicle releases; correlated release or short-term plasticity require extension.
- The analytical FPT solution assumes diffusion-like statistics; Poisson input with large quanta may need exact simulation.
Related Concepts
- Integrate-and-fire neurons
- Coefficient of variation
- Spike-frequency adaptation
- Post-inhibitory rebound
- First-passage-time analysis
- Excitatory-inhibitory balance
- Quantal content / synaptic vesicle release
Activation
inter-spike interval, ISI statistics, adaptive threshold, EI circuit, first-passage time, spike variability, integrate-and-fire, post-inhibitory rebound, quantal content, neuronal noise