Biology:Exponential integrate-and-fire

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Short description: Spiking neuron model

In biology exponential integrate-and-fire models are compact and computationally efficient nonlinear spiking neuron models with one or two variables. The exponential integrate-and-fire model was first proposed as a one-dimensional model.[1] The most prominent two-dimensional examples are the adaptive exponential integrate-and-fire model[2] and the generalized exponential integrate-and-fire model.[3] Exponential integrate-and-fire models are widely used in the field of computational neuroscience and spiking neural networks because of (i) a solid grounding of the neuron model in the field of experimental neuroscience, (ii) computational efficiency in simulations and hardware implementations, and (iii) mathematical transparency.

Exponential integrate-and-fire (EIF)

The exponential integrate-and-fire model (EIF) is a biological neuron model, a simple modification of the classical leaky integrate-and-fire model describing how neurons produce action potentials. In the EIF, the threshold for spike initiation is replaced by a depolarizing non-linearity. The model was first introduced by Nicolas Fourcaud-Trocmé, David Hansel, Carl van Vreeswijk and Nicolas Brunel.[1] The exponential nonlinearity was later confirmed by Badel et al.[4] It is one of the prominent examples of a precise theoretical prediction in computational neuroscience that was later confirmed by experimental neuroscience.

In the exponential integrate-and-fire model,[1] spike generation is exponential, following the equation:

[math]\displaystyle{ \frac{dV}{dt} - \frac{R} {\tau_m} I(t)= \frac{1} {\tau_m}[E_m-V+\Delta_T \exp \left( \frac{V - V_T} {\Delta_T} \right)] }[/math].
Parameters of th exponential integrate-and-fire neuron can be extracted from experimental data.[4]

where [math]\displaystyle{ V }[/math] is the membrane potential, [math]\displaystyle{ V_T }[/math] is the intrinsic membrane potential threshold, [math]\displaystyle{ \tau_m }[/math] is the membrane time constant, [math]\displaystyle{ E_m }[/math]is the resting potential, and [math]\displaystyle{ \Delta_T }[/math] is the sharpness of action potential initiation, usually around 1 mV for cortical pyramidal neurons.[4] Once the membrane potential crosses [math]\displaystyle{ V_T }[/math], it diverges to infinity in finite time.[5][4] In numerical simulation the integration is stopped if the membrane potential hits an arbitrary threshold (much larger than [math]\displaystyle{ V_T }[/math]) at which the membrane potential is reset to a value Vr . The voltage reset value Vr is one of the important parameters of the model.

Two important remarks: (i) The right-hand side of the above equation contains a nonlinearity that can be directly extracted from experimental data.[4] In this sense the exponential nonlinearity is not an arbitrary choice but directly supported by experimental evidence. (ii) Even though it is a nonlinear model, it is simple enough to calculate the firing rate for constant input, and the linear response to fluctuations, even in the presence of input noise.[6]

A didactive review of the exponential integrate-and-fire model (including fit to experimental data and relation to the Hodgkin-Huxley model) can be found in Chapter 5.2 of the textbook Neuronal Dynamics.[7]

Adaptive exponential integrate-and-fire (AdEx)

Initial bursting AdEx model

The adaptive exponential integrate-and-fire neuron [2] (AdEx) is a two-dimensional spiking neuron model where the above exponential nonlinearity of the voltage equation is combined with an adaptation variable w

[math]\displaystyle{ \tau_m \frac{dV}{dt} = R I(t) + [E_m-V+\Delta_T \exp \left( \frac{V - V_T} {\Delta_T} \right)] - R w }[/math]

[math]\displaystyle{ \tau \frac{d w (t)}{d t} = - a [V_\mathrm{m} (t) - E_\mathrm{m} ]- w + b \tau \delta (t-t^f) }[/math]

where w denotes an adaptation current with time scale [math]\displaystyle{ \tau }[/math]. Important model parameters are the voltage reset value Vr, the intrinsic threshold [math]\displaystyle{ V_T }[/math], the time constants [math]\displaystyle{ \tau }[/math] and [math]\displaystyle{ \tau_m }[/math] as well as the coupling parameters a and b. The adaptive exponential integrate-and-fire model inherits the experimentally derived voltage nonlinearity [4] of the exponential integrate-and-fire model. But going beyond this model, it can also account for a variety of neuronal firing patterns in response to constant stimulation, including adaptation, bursting and initial bursting.[8]

The adaptive exponential integrate-and-fire model is remarkable for three aspects: (i) its simplicity since it contains only two coupled variables; (ii) its foundation in experimental data since the nonlinearity of the voltage equation is extracted from experiments;[4] and (iii) the broad spectrum of single-neuron firing patterns that can be described by an appropriate choice of AdEx model parameters.[8] In particular, the AdEx reproduces the following firing patterns in response to a step current input: neuronal adaptation, regular bursting, initial bursting, irregular firing, regular firing.[8]

A didactic review of the adaptive exponential integrate-and-fire model (including examples of single-neuron firing patterns) can be found in Chapter 6.1 of the textbook Neuronal Dynamics.[7]

Generalized exponential integrate-and-fire Model (GEM)

The generalized exponential integrate-and-fire model[3] (GEM) is a two-dimensional spiking neuron model where the exponential nonlinearity of the voltage equation is combined with a subthreshold variable x

[math]\displaystyle{ \tau_m \frac{dV}{dt} = R I(t) + [E_m-V+\Delta_T \exp \left( \frac{V - V_T} {\Delta_T} \right)] - b \, [E_x-V] x }[/math]

[math]\displaystyle{ \tau_x(V) \frac{d x (t)}{d t} = x_0(V_\mathrm{m} (t))- x }[/math]

where b is a coupling parameter, [math]\displaystyle{ \tau_x(V) }[/math] is a voltage-dependent time constant, and [math]\displaystyle{ x_0(V) }[/math] is a saturating nonlinearity, similar to the gating variable m of the Hodgkin-Huxley model. The term [math]\displaystyle{ b [E_x-V] x }[/math] in the first equation can be considered as a slow voltage-activated ion current.[3]

The GEM is remarkable for two aspects: (i) the nonlinearity of the voltage equation is extracted from experiments;[4] and (ii) the GEM is simple enough to enable a mathematical analysis of the stationary firing-rate and the linear response even in the presence of noisy input.[3]

A review of the computational properties of the GEM and its relation to other spiking neuron models can be found in.[9]

References

  1. 1.0 1.1 1.2 Fourcaud-Trocmé, Nicolas; Hansel, David; van Vreeswijk, Carl; Brunel, Nicolas (2003-12-17). "How Spike Generation Mechanisms Determine the Neuronal Response to Fluctuating Inputs" (in en). The Journal of Neuroscience 23 (37): 11628–11640. doi:10.1523/JNEUROSCI.23-37-11628.2003. ISSN 0270-6474. PMID 14684865. 
  2. 2.0 2.1 "Adaptive exponential integrate-and-fire model as an effective description of neuronal activity". Journal of Neurophysiology 94 (5): 3637–42. November 2005. doi:10.1152/jn.00686.2005. PMID 16014787. https://journals.physiology.org/doi/full/10.1152/jn.00686.2005. 
  3. 3.0 3.1 3.2 3.3 Richardson, Magnus J. E. (2009-08-24). "Dynamics of populations and networks of neurons with voltage-activated and calcium-activated currents" (in en). Physical Review E 80 (2): 021928. doi:10.1103/PhysRevE.80.021928. ISSN 1539-3755. PMID 19792172. Bibcode2009PhRvE..80b1928R. https://link.aps.org/doi/10.1103/PhysRevE.80.021928. 
  4. 4.0 4.1 4.2 4.3 4.4 4.5 4.6 4.7 "Dynamic I-V curves are reliable predictors of naturalistic pyramidal-neuron voltage traces". Journal of Neurophysiology 99 (2): 656–66. February 2008. doi:10.1152/jn.01107.2007. PMID 18057107. 
  5. "How connectivity, background activity, and synaptic properties shape the cross-correlation between spike trains". The Journal of Neuroscience 29 (33): 10234–53. August 2009. doi:10.1523/JNEUROSCI.1275-09.2009. PMID 19692598. 
  6. Richardson, Magnus J. E. (2007-08-20). "Firing-rate response of linear and nonlinear integrate-and-fire neurons to modulated current-based and conductance-based synaptic drive". Physical Review E 76 (2): 021919. doi:10.1103/PhysRevE.76.021919. PMID 17930077. Bibcode2007PhRvE..76b1919R. https://link.aps.org/doi/10.1103/PhysRevE.76.021919. 
  7. 7.0 7.1 Gerstner, Wulfram. Neuronal dynamics : from single neurons to networks and models of cognition. Kistler, Werner M., 1969-, Naud, Richard, Paninski, Liam. Cambridge. ISBN 978-1-107-44761-5. OCLC 885338083. https://www.worldcat.org/oclc/885338083. 
  8. 8.0 8.1 8.2 "Firing patterns in the adaptive exponential integrate-and-fire model". Biological Cybernetics 99 (4–5): 335–47. November 2008. doi:10.1007/s00422-008-0264-7. PMID 19011922. 
  9. Brunel, Nicolas; Hakim, Vincent; Richardson, Magnus JE (2014-04-01). "Single neuron dynamics and computation" (in en). Current Opinion in Neurobiology. Theoretical and computational neuroscience 25: 149–155. doi:10.1016/j.conb.2014.01.005. ISSN 0959-4388. PMID 24492069. http://www.sciencedirect.com/science/article/pii/S0959438814000130.