- Journal List
- NIHPA Author Manuscripts
- PMC2570441

# Two computational regimes of a single-compartment neuron separated by a planar boundary in conductance space

^{1}Department of Physiology and Biophysics, University of Washington, Seattle

^{2}Veterans Affairs Puget Sound Health Care System, Seattle, Washington

## Abstract

Recent *in vitro* data show that neurons respond to input variance with varying sensitivities. Here, we demonstrate that Hodgkin-Huxley (HH) neurons can operate in two computational regimes, one that is more sensitive to input variance (differentiating) and one that is less sensitive (integrating). A boundary plane in the 3D conductance space separates these two regimes. For a reduced HH model, this plane can be derived analytically from the *V* nullcline, thus suggesting a means of relating biophysical parameters to neural computation by analyzing the neuron’s dynamical system.

## Introduction

A neuron’s ion channel configuration determines how it processes information. However, the relationship between a particular set of ion channels and the specific computation it performs is still not clear, even for basic Hodgkin-Huxley (HH) model neurons (Hodgkin and Huxley, 1952; Aguera y Arcas et al., 2003; Yu and Lee, 2003) and simplified versions of the model (Kepler et al., 1992; Gerstner and Kistler, 2002; Murray, 2002). In this paper, we examine information processing in the HH neuron, where this model neuron is taken to be a generic case with typical spike-triggering ion channels. We focus on the response of the space-clamped HH model to a time-varying synaptic current input.

We approximate the net synaptic current input at the soma as exponentially-filtered Gaussian white noise current (Gerstein and Mandelbrot, 1964; Bryant and Segundo, 1976; Tuckwell, 1988; Mainen and Sejnowski, 1995; Destexhe et al., 2001; Rauch et al., 2003; Rudolph and Destexhe, 2003a; Richardson and Gerstner, 2005), in which the input mean reflects the average number of inputs while fluctuations, quantified by the variance, generally depend on the degree of neuronal input synchrony (Destexhe and Pare, 1999; Moreno et al., 2002; Richardson, 2004). We use the firing rate-current (*f-I*) function as a straightforward means of examining the model’s input/output response properties. If firing rate varies most strongly with mean current, we term the neuron an *integrator*; if the firing rate is sensitive to variance and relatively insensitive to the mean current, the neuron is fluctuation-driven, and we refer to it as a *differentiator* (Abeles, 1982; Konig et al., 1996; Higgs et al., 2006). A differentiating neuron is thus characterized by low or zero firing rate in response to a constant or zero variance input.

Naturally, a spectrum exists between these two classifications. In addition, the operating mode of a given neuron often depends on the mean input current. Many neurons function as differentiators at low, subthreshold mean currents but behave more like integrators at suprathreshold mean currents; other neurons differentiate their input at saturating mean currents. However, the purest neural differentiators, such as specialized coincidence detectors in the auditory brainstem (Oertel, 1983; Reyes et al., 1994; Rothman and Manis, 2003) appear entirely incapable of integration, and never fire repetitively at any level of constant current stimulation.

Modeling studies suggest that neurons can function as either integrators or coincidence detectors (differentiators) based on the nature of incoming input (Gutkin et al., 2003; Rudolph and Destexhe, 2003b). *In vitro* studies suggest that high conductance inputs facilitate coincidence detection, or differentiation (Gonsalves and Paller, 2000; Destexhe et al., 2003; Prescott et al., 2006), and at least one *in vivo* study suggests that synchronized inputs more effectively drive cortical spiking (Roy and Alloway, 2001). Recent *in vitro* studies suggest that neuronal firing rates are affected by the statistical properties of approximated synaptic inputs (Chance et al., 2002; Fellous et al., 2003), and that different populations of neurons respond to input variance with differing sensitivities (Higgs et al., 2006; Arsiero et al., 2007).

Our aim was to determine the biophysical parameter regime for which the HH neuron retains sensitivity to input variance even at high input means. We conclude that the HH neuron can process information in two fundamental ways, as both an integrator and a differentiator, and that, despite the highly nonlinear nature of the model, a planar boundary in the space of maximal conductances separates these two regimes. Further, using a 2D simplification of the HH model, we find that this planar boundary can be derived directly from model equations and related dynamical system properties, thus demonstrating a simple link between the observed categories of computational function and the biophysical conductance parameters.

## Hodgkin-Huxley neuron as both integrator and differentiator

Recent studies show that *f-I* curves from *in vitro* cortical pyramidal cells, hippocampal CAI pyramidal cells, and neurons from avian auditory brainstem demonstrate changes in sensitivity to input variance as the mean is increased, and suggest that these changes are related to slow adaptation currents (Higgs et al., 2006; Prescott et al., 2006) or slow sodium inactivation (Arsiero et al., 2007). However, many simple neuron models, including the standard Hodgkin-Huxley (HH) model neuron, the Connor-Stevens model neuron, and the Traub-Miles model neuron, show decreased sensitivity to input variance as the mean increases. We have found that for several simple model neurons, lowering the maximal sodium conductance *G*_{Na}, such as through voltage-dependent slow sodium inactivation, leads to an increased sensitivity to input variance at high means, as would be the case for differentiating neurons (Figure 1). In this differentiator operating regime, these neurons do not fire repetitively to constant, or zero-variance, inputs.

**Spectrum of integration and differentiation. (a) Simple differentiators do not respond to zero variance inputs at steady state**

Here, we consider only static maximal conductance values rather than any activity-dependent (LeMasson et al., 1993; Giugliano et al., 1999) or voltage-dependent change. The membrane potential (*V*) of the space-clamped Hodgkin-Huxley (HH) neuron is described by

where *C* is capacitance, *G _{i}* are the maximal channel conductances,

*E*are the reversal potentials,

_{i}*I*is the external, injected current, and

*[m, h, n]*are the channel gating variables, which obey first order dynamics (Appendix A). If we take this standard HH neuron and systematically lower its maximal sodium conductance, its response to inputs, as evaluated by an

*f-I*curve, changes (Figure 2). When

*G*

_{Na}is high, the HH neuron behaves more like an integrator, while when

*G*

_{Na}is low, the neuron behaves more like a differentiator.

Conceptually, these differences in the *f-I* curves (Figure 1, gray and black) result from changes in an effective voltage threshold for spiking, where spike initiation occurs when enough sodium channels open to counter outward currents. The maximal conductance *G*_{Na}, for example, approximately establishes the spiking threshold. Additionally, the availability of sodium channels depends on the voltage-dependent inactivation variable *h*, adjusting the effective threshold value. Differentiation then occurs when slow components of the input are below this threshold, and firing only results from input noise. In certain regimes, such as when *G*_{Na} has been lowered sufficiently, this effective threshold is never surpassed as input mean increases – the voltage-dependent threshold keeps increasing slightly as the input mean increases until eventually the neuron is unable to spike. This effect, known as depolarization block, is observed for large inputs in the *f-I* curves of Figure 2. This conceptual explanation will be further developed in terms of the neuron’s dynamical system.

## A planar boundary separates integration from differentiation

We simulated the HH model using a set of 56 different conductance values (*G*_{Na}*, G*_{K}*, G*_{Leak}) and from these determined *f-I* curves from each condition. As seen in Figure 2, at high *G*_{Na} the HH neuron responds well to noiseless inputs, whereas at low *G*_{Na} the neuron does not respond to zero-variance inputs. This transition from noiseless firing to no response is relatively sudden along the range of *G*_{Na} in which firing occurs. This transition can also be observed when *G*_{K} or *G*_{Leak} are increased, or when these three conductances are modulated in linear combination according to^{1}:

where conductances have units mS/cm^{2}. When this sum is less than zero, the HH neuron will not fire to a noiseless current, whereas if the sum is greater than zero, the neuron fires repetitively. Eq. (2) describes the empirically observed plane that passes through the origin in the three-dimensional space of HH conductances, which is shown as a line for fixed *G*_{Leak} in Figure 3a. Here, if the neuron does not fire to a noiseless current, no matter how large the mean, then the neuron is considered to behave more like a differentiator^{2}. In terms of the dynamical system, when the right hand side of Eq. (2) is greater than zero, the system undergoes a Hopf bifurcation at a particular mean current (e.g. approx 6.5 μA/cm^{2} in Figure 1b, bottom black trace); however, if the right hand side is less than zero, the one fixed point of the dynamical system is stable for all mean current values (as in Figure 5b and c).

**The boundary between no response to constant stimuli (differentiation) and firing to constant stimuli (integration) is described by a line in the two-dimensional space of**

*G*_{Na}and*G*_{K}Having obtained Eq. (2) through simulation, we would like to derive it directly from model equations. However, due to its four differential equations, the dynamical system of the HH model is difficult to analyze. Therefore, we use the two-dimensional Abbott-Kepler (AK) model, which is derived from the HH model equations and maintains a direct correspondence of parameters (Abbott and Kepler, 1990; Kepler et al., 1992). In the AK model, the four variables of the HH model (*V, m, h,* and *n*) are divided by time scale into two groups that become *V* and *U*, a fast activation and a slow recovery variable, respectively. The 2D AK model equations have the form (Abbott and Kepler, 1990; Kepler et al., 1992; Hong et al., In press):

Eq. (3) has a similar form to Eq. (1), where the dynamics of the gating variables have been replaced by their steady state voltage-dependent values *m*_{∞}, *n*_{∞} and *h*_{∞}. Like the HH model, this model shows a boundary plane between integration and differentiation, which is described by^{3}:

where conductances have units mS/cm^{2}. The line that is described by Eq. (5) when *G*_{Leak} = *0.3* mS/cm^{2} is shown in Figure 3b.

## Deriving the planar boundary

The advantage of working with a two-dimensional dynamical system is that we can more easily understand how the empirical boundary equation, Eq. (5), emerges from the dynamical system, Eqs. (3) and (4). We begin from the phase portrait of the AK model. The flow is determined by the *V* and *U* nullclines, defined as the set of points for which *dV*/*dt* = 0 and *dU*/*dt* = 0, respectively. The unique fixed point of the system is the point of intersection of the two nullclines (Gerstner and Kistler, 2002; Murray, 2002; Izhikevich, 2007). In the AK model, from Eq. (4), the *U* nullcline is given by *U*=*V*. The *V* nullcline generally takes an N-shape for intrinsically spiking neural models (Izhikevich, 2007), and is given by the solution of

which for simplicity we express as

where

Thus, for the AK model, the shape of the *V* nullcline in *(V,U)* space depends nonlinearly on mean current *I* as well as on the parameters of Eq. (7). We will focus on the three maximal conductances *(G*_{Na}*, G*_{K}*, G*_{Leak}*)*.

For any given set of the four parameters *(G*_{Na}*, G*_{K}*, G*_{Leak}, *I)*, whether or not the neuron fires in response to DC current is determined by two things: the shape of the *V* nullcline and the position of the fixed point on this nullcline. If the *V* nullcline has an *N*-like shape, as seen in Figure 4a and b, the system is excitable. However, for some values of *I*, the *V* nullcline can flatten and the system becomes unable to create a spike; this corresponds to depolarization block and is seen in the top contour of Figure 5a, which is the *V* nullcline for *I*=*40* μA/cm^{2} and the given conductances. When the system is able to spike, the second factor determining DC response is where the fixed point, the intersection of the *V* nullcline with the line *U* = *V*, lies with respect to the *local minimum* of the *V* nullcline or the left “knee” of the curve. When the fixed point is to the right of the knee, the neuron fires repetitively to zero-variance mean current (Figure 4a, 4c), but when the fixed point is to the left of the local minimum it does not (Figure 4b, 4d)^{4}.

When the current is noisy, the position of the fixed point with respect to the minimum determines whether spike initiation is largely dictated either by the internal dynamics of the system (Figure 4c) or by momentary, large current fluctuations (Figure 4d). These fluctuations cause leftward or rightward excursions along the V-axis, which may cause the neuron to cross an upward curving threshold function situated slightly beneath, but approximately parallel to, the V nullcline (Hong et al., In press). If a change in stimulus is gradual, the nullclines alter their geometry, which may prevent threshold crossing despite an equally large or larger stimulus perturbation.

Each point in the parameter space *(G*_{Na}*, G*_{K}*, G*_{Leak}, *I)* maps onto one of three possible conditions: no minimum exists in the *V* nullcline and thus the system is not excitable; or the system is excitable, with a fixed point either to the right or the left of the minimum. For the AK model to implement a perfect differentiator, it should not fire spontaneously for any mean current level *I*. For this to be the case, for values of *I* such that the *V* nullcline shows a minimum, the nullclines must have the configuration of Figure 4b or 4d. Thus, as *I* increases, the *V*-nullcline minimum will disappear before the fixed point shifts to the right of the *V* nullcline minimum. We use this to derive the boundary condition on conductance parameters.

Let us consider an example of the behavior of the system. In Figure 5a, we show contours of the surface Eq. (7), which are a set of *V* nullclines each for different *I*. As *I* increases, the nullclines lose their *N*-like shape, and eventually the neuron is no longer excitable and undergoes depolarization block. For differentiating neurons, the line *U* = *V* always intersects the *V* nullclines at a place where the *V* nullcline is decreasing, i.e. the derivative of the *V* nullcline evaluated at the fixed point is negative: as can be seen in Figure 5, this means that *f*/*V* > 0. A boundary conductance (*G*_{Na}*, G*_{K}*, G*_{Leak}) gives, then, a set of *I*-dependent *V* nullclines for which this partial derivative has a minimum value of zero, as in Figure 5d.

For the fixed point to occur to the left of the minimum, we require that *dU*/*dV* < *0* for all fixed points (*U*_{0}(*I*),*V*_{0}(*I*)). Thus, the condition is given by

One of the two fixed-point conditions is that all fixed points, independent of *I*, must satisfy *U* = *V*. Thus, fixed points for all *I* fall somewhere along the line *U* = *V*. Since we want to characterize the system’s behavior for all *I*, we will thus evaluate the condition at *U* = *V*. Further, we will only consider the numerator of Eq. (8) (see also Appendix B), giving the condition

Figure 5d shows some examples of the function *f*/*V*, evaluated for several values of the conductances. Our boundary criteria require not only that the derivative is zero, but that zero is the minimal value for any *I*. Thus, at the point (*V _{0}(I**

*),U**

_{0}(I*)*), where the derivative takes the value zero, the function

*f*/

*V*must be at a minimum. Hence, we require that for some value of

*V*,

*V** =

*V**

_{0}(I*)*, where

*V** is a function of

*I*and the conductance parameters, Eq. (9) and the following hold simultaneously:

Because both boundary equations Eqs. (9) and Eq. (10) are homogenous in *G*_{Na}*, G*_{K} and *G*_{Leak}, we can describe the boundary plane with two variables. For example, we can rewrite Eq. (9) as:

where *N* and *K* are conductance ratios. From Eq. (10), we obtain another constraining equation and must then solve the following system:

where *A*_{1} and *B*_{1} are coefficients of Eq. (9) as written explicitly in Eq. (11),

and *A*_{2} and *B*_{2} are coefficients of Eq. (10),

The general solution is:

The forms of *N* and *K* are highly nonlinear due to the dependence on the unknown value *V** (Figure 6a), where *V** > −51 mV for positive conductance ratios. Rather than solve for *V** for every parameter set, we observe that the relevant range of *V** is highly constrained by the need to generate conductance values in a physiological range. The range used, *V** = [−50.5 −48]*,* gives *N* = [50 500], which was a constraint for the simulation. In this very narrow range of *V**, *N* and *K* are linearly related to one another; these are plotted against one another in Figure 6b. When we fit the line of *N vs. K*, we obtain coefficients of ~1.55 and 16.5, which are very close to the coefficients of *G*_{K} and *G* _{Leak} in Eq. (5), respectively. Exact agreement between simulated and calculated results is probably prevented by imprecision in gathering the simulated boundary points.

**Conductance ratios**

*N*=*G*_{Na}/*G*_{Leak}and*K*=*G*_{K}/*G*_{Leak}plotted (a) as functions of*V*and (b) against each otherThe coefficients of *G*_{K} and *G*_{Leak} in Eq. (5) can be determined analytically from the coefficients *A*_{1} and *B*_{1} of Eq. (11). Specifically, for a given value *V**, the coefficient for *G*_{K} is −*B* _{1}(*V**)/*A*_{1}(*V**) and the coefficient for *G*_{Leak} is −*1*/*A*_{1}(*V**), as plotted in Figure 6c and 6d. Given Eq. (13), −*B*_{1}/*A*_{1} and −*1*/*A*_{1} are the slope and *y*-intercept of the linear relationship *N vs. K*. Regression, as in Figure 6b, takes into account many values of *V** and does not require knowing *V** *a priori*, while using *A*_{1} and *B*_{1} gives an analytic result for a given *V**.

## Hodgkin-Huxley boundary equation

The coefficients of the HH boundary equation, Eq. (2), differ by a constant from those of the AK boundary, Eq. (5). The HH model is less excitable than the AK model, since less outward conductance is needed to suppress firing. In the approximations made in the 2D reduction of HH to AK, the largest source of error probably stems from the approximation of infinitely fast dynamics for the sodium activation variable, such that *m* ≈ *m*_{∞}. Around the typical voltage threshold, *m* has a time constant of ~0.3–0.5 msec. This will cause the true *m* to lag behind the approximated *m* ≈ *m*_{∞} and to take a lower value at any point in time leading up to the threshold, causing the increased excitability of the AK model. Comparing *m* dynamics during spiking near the boundary with those of *m _{∞}* (not shown), we find that multiplying

*m*by a constant factor of 3/4 provides a better approximation to

_{∞}*m*around the threshold. When this factor is included in the AK model, the boundary equation coefficients extracted from simulations are found to be 2.09 and 22.14, in good agreement with those determined by the HH equations in Eq. (2). With this correction, the

*V-*nullcline of Eq. (9) can be used to analytically find the coefficients as above

^{5}: 2.07 and 21.3.

## Slow sodium inactivation

While we have considered only steady state conductances, this approach may help to conceptualize the behavior of a system subject to certain types of adaptation, such as slow sodium inactivation (Arsiero et al., 2007). That the addition of slow sodium inactivation effectively lowers maximal sodium conductance for steady state can be seen from the model equations. Slow sodium inactivation may be introduced (Fleidervish et al., 1996; Miles et al., 2005) through an additional slow sodium inactivation variable *s*:

where *s* has the same form as the inactivation variable *h* but with a much slower time constant. The addition of *s* lowers the effective sodium pool for spiking. At steady state, when *s* is approximately constant due to its slow kinetics relative to spiking, this addition is equivalent to lowering *G*_{Na}. Through the sigmoidal voltage dependence of *s*, changes in mean current leads to effective changes of *G*_{Na}; as mean current increases, *s* decreases, decreasing the effective sodium pool. In other words, in contrast to spike-dependent adaptation currents, the voltage dependence of sodium inactivation provides feedback regardless of spiking activity. Thus, slow sodium inactivation, which in some sense is similar to voltage-dependent adaptation currents (Benda and Herz, 2003), is one mechanism by which the functional role of a neuron could change from integrating to differentiating without changes in channel density.

## Discussion

Models of a variety of neurons share the same form as the Hodgkin-Huxley (HH) neuron (Ermentrout, 1998; Shriki et al., 2003), and evidence suggests that single-compartment models can capture key properties of *in vivo* and *in vitro* neurons (Destexhe et al., 2001). Here, we show specifically how a ratio of inward and outward conductances affect the HH neuron’s sensitivity to input variance. The balance of outward to inward currents affects neuronal excitability. The well-known coincidence detection of auditory neurons (Reyes et al., 1996; Trussell, 1997) is enhanced by both a low-threshold potassium channel, which effectively decreases the membrane time constant (Reyes et al., 1994; Rathouz and Trussell, 1998; Rothman and Manis, 2003), and low availability of sodium channels (Svirskis et al., 2004). In dendrites, membrane excitability is modulated by changes in sodium or potassium currents (Colbert et al., 1997; Johnston et al., 1999). Low sodium conductance, which leads to spike frequency adaptation, may be the result of intrinsic low channel density (Melnick et al., 2004) or slow sodium inactivation (Fleidervish et al., 1996; Miles et al., 2005), which can be modulated by second messenger systems (Cantrell and Catterall, 2001).

Neurons demonstrate a spectrum of integration and differentiation, and slow adaptation currents may correlate with shifts along this spectrum, at least for more complicated neurons such as neocortical pyramidal neurons (Higgs et al., 2006). However, diverging *f-I* curves, as in Figure 2 or Arsiero *et al.* (2007), would more likely be related to voltage-dependent rather than spike-dependent adaptation. Previous work has demonstrated that increased shunting, a likely consequence of strong excitatory and inhibitory synaptic input, can allow *M*-current adaptation to effectively switch a neuron’s operating regime from integration to coincidence detection, or differentiation (Prescott et al., 2006). This may be a specific case of our general result, where the *M*-current essentially increases *G*_{K} and shunting increases *G*_{Leak}. In some cases, the synaptic conductance alone may be large enough to switch a neuron from integration to differentiation. For example, Destexhe and Paré (1999) found that the input resistance of pyramidal cells in the parietal cortex decreases approximately five-fold during intense network activity. In the standard HH model, our results indicate that this change would place the cell near the boundary between integrator and differentiator function. Because synaptic conductances are highly variable on both short and long time scales, a postsynaptic neuron may fluctuate dynamically across the functional boundary.

Although we divide neural behavior into integration and differentiation as classified by the variance dependence of *f-I* curves, there are other possible ways to determine the computation that a single neuron performs on its current inputs. One example is white noise analysis, which we have explored extensively in applications to the Hodgkin-Huxley model (Aguera y Arcas et al., 2003), reduced models (Aguera y Arcas and Fairhall, 2003; Hong et al., In press), and neurons of avian brainstem (Slee et al., 2005). While we have found, suggestively, that the computation as described by a linear/nonlinear model changes as a function of G_{Na}/G_{K} (R. Mease, unpublished data), here we do not attempt to connect these results.

In conclusion, we find that a plane separates two computational regimes in the space of maximal ionic conductances in the Hodgkin-Huxley and Abbott-Kepler models. Hyperplanes have been noted to separate models with different firing characteristics (Goldman et al., 2001; Taylor et al., 2006); in this case we show how the plane can be derived from characteristics of the *V* nullcline. Since *V* nullclines for reduced models of neuronal dynamics can in principle be obtained experimentally from *I(V)* plots (Izhikevich, 2007), this method may provide a means of relating biophysical properties with computational ones. Specifically, one may be able to infer certain biophysical parameters and their related effect on the neuron’s computation from an experimentally obtained set of *I(V)* plots. Finally, although we focus here on maximal conductances, as might be regulated by homeostatic mechanisms, many forms of adaptation, such as slow sodium inactivation, change conductances over time, so that each adaptation state has a different maximal conductance. Time-dependent movement of the system through different computational states may be an effective way to describe the functional role of adaptation.

## Acknowledgments

We thank W. J. Spain, Rebecca Mease, Michele Giugliano, and Larry Sorenson for helpful discussions and Michele Giugliano for comments on the manuscript. This work was supported by a Burroughs-Wellcome Careers at the Scientific Interface grant and a Sloan Research Fellowship to ALF; BNL was supported by the Medical Scientist Training Program, a fellowship from the National Institute of General Medical Sciences (T32 07266) and an ARCS fellowship; MHH was supported by a VA Merit Review to WJS. This project was also supported by Grant Number F30NS055650 (to BNL) from the National Institute Of Neurological Disorders And Stroke. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institute Of Neurological Disorders And Stroke or the National Institutes of Health.

## Appendix A: Biophysical Modeling

The single-compartmental conductance-based Hodgkin-Huxley (HH) model neuron (Hodgkin and Huxley, 1952) was used with standard parameters (Koch, 1999; Dayan and Abbott, 2001; Gerstner and Kistler, 2002) except as noted. In addition to Eq. (1), the following equations comprise the HH model:

where steady state gating values, such as *n _{∞}*, are equal to

*α*/

*(α*+

*β)*. Standard parameters for HH are:

*G*

_{Na}=

*120*,

*G*

_{K}=

*36*, and

*G*

_{Leak}=

*0.3*mS/cm

^{2};

*E*

_{Na}=

*50*,

*E*

_{K}= −

*77*, and

*E*

_{Leak}= −

*54.4*mV; and

*C*=

*1 μF*/

*cm*. For the cortical neuron model of Figure 1, standard parameters are:

^{2}*G*

_{Na}=

*50*,

*G*

_{Kfast}=

*225*,

*G*

_{Kslow}=

*0.225,*and

*G*

_{Leak}=

*0.25*mS/cm

^{2};

*E*

_{Na}=

*74*,

*E*

_{Kfast}=

*E*

_{Kslow}= −

*90*, and

*E*

_{Leak}= −

*70*mV; and

*C*=

*1 μF*/

*cm*.

^{2}Equations for the Abbott-Kepler model are derived from the HH model (Abbott and Kepler, 1990; Kepler et al., 1992; Hong et al., In press). Equations were solved numerically using fourth-order Runge-Kutta integration with a fixed time step of 0.05 msec, or 0.025 msec for the AK model. Injected current was simulated by a series of normally-distributed random numbers that were smoothed by an exponential filter (τ = 1 msec). Spike times were identified as the upward crossing of the voltage trace at −20 mV (resting potential = −65 mV) separated by more than 2 msec.

## Appendix B: Examining *f(U,V)*

That Eq. (9) is the appropriate condition can also be seen as follows. While the function *f* depends on both *U* and *V*, along the nullclines, *U* is a function of *V, U=g(V)*. Thus, requiring *df(U,V)*/*dV* = *0* at the fixed point as required by the definition of a *V* nullcline:

where *f*/*U* > 0. Then, the numerator must equal zero, giving Eq. (9). One can show that the full stability analysis around a fixed point gives almost the same result as our discussion based on the shape of a nullcline. For the 2D AK model, the following two conditions on the determinant and trace of the Jacobian matrix *J* evaluated at the fixed point determine the stability of the fixed point (Strogatz, 1994):

where *F(U,V)* = −*f(U,V)*/*C* +*I*/*C* = *dV*/*dt*, given Eq. (7), and *g(U,V)* = *dU*/*dt*. The first condition is always satisfied for AK models, as the Jacobian at fixed points of these models always have complex eigenvalues due to their resonating dynamics. For the *U* nullcline of the AK model, *g* ≈ −*k*(*U*−*V*), where *k* has the form:

The functions *t _{i}*(

*V*) are slowly varying functions that are of the same order of magnitude over the range of

*V*that we are interested in. Therefore,

*k*weakly depends on conductances and is roughly constant in

*V*. Moreover, the value of

*k*is small with a maximum value less than 0.3 mV/msec. Therefore, $\frac{\partial f}{\partial V}=-C\frac{\partial F}{\partial V}\lesssim 0.3\phantom{\rule{0.16667em}{0ex}}\text{mS}/{\text{cm}}^{2}$ is approximately equivalent to a full stability analysis based on the Jacobian. Even when

*k*is nonzero, there isn’t a qualitative change; since $\frac{\partial f}{\partial V}={G}_{\text{Leak}}+(V\phantom{\rule{0.16667em}{0ex}}\text{dependent}\phantom{\rule{0.16667em}{0ex}}\text{terms})$, considering non-zero constant

*k*is equivalent to

*G*

_{Leak}→

*G*

_{Leak}+

*k*, which corresponds to a small offset of our boundary plane such that it does not pass through the origin. Thus, the right hand side of Eqs. (2) and (5) may not equal zero. When we fit our simulated data and allow for a nonzero offset, the coefficients and error of the fit are almost identical as previously, and the fitted offset is small (HH: ~−0.3; AK: ~1.0).

## Footnotes

^{1}These coefficients are the result of a multiple least squares regression of 56 conductance sets *(G*_{Na}*, G*_{K}*, G*_{Leak}*)* determined via simulation. For a given *G*_{Na} and *G*_{Leak}, *G*_{K} would initially take a relatively low value for which the neuron would fire to some mean input current *I. G*_{K} was then increased incrementally and *f-I* curves computed until the neuron would not fire to any mean input *I*; this was then one of the boundary sets. As the ratios of the conductances (i.e. *N* = *G*_{Na}/*G*_{Leak} and *K* = *G*_{K}/*G*_{Leak}) increased, the steady state voltages *V _{0}* at the boundary current value (which we will later define as

*I**) generally decreased: mean −52.8; std 2.0; range [−48.6–54.8]. Conductances were chosen according to the following constraints:

*N*was within the range [50 500],

*G*

_{Na}>

*50 mS*/

*cm*

^{2}, G_{Leak}=

*0.3*,

*1*, or

*2*. The best fit of these data passes through or very close to the origin (Appendix B).

^{2}Although for the HH model this is an appropriate criterion, other models can show non-zero firing rates in response to zero-variance stimuli while their *f-I* curves are differentiator-like as in Figure 2. Further, even neurons that are here classified as integrators, as seen on the left side of Figure 2, display differentiator-like characteristics when mean input currents are low.

^{3}This process was the same as for the HH model for 55 conductance sets. Again, as conductance ratios (i.e. *N* = *G*_{Na}/*G*_{Leak} and *K* = *G*_{K}/*G*_{Leak}) increased, steady states voltages *V _{0}* at the boundary current value (which we will later define as

*I**) decreased: mean −50.3; std 0.8; range [−48.2–51.2]. The best fit of these data passes through or very close to the origin (Appendix B).

^{4}This may not be strictly true. As has been noted for the Fitzhugh-Nagumo model (Izhikevich, 2007), loss of stability by the fixed point may not occur precisely at the local minimum in the *V*-nullcline, as can be verified by linearization and local stability analysis. The effect is small in the AK model (Appendix B).

^{5}This is, of course, not a true *V*-nullcline of the HH model since we are not specifying a dependent variable to plot it against. But, as in the AK case, we assume that that the slow gating variables *n* and *h* are not functions of *V* and can then be ignored when partial differentiating with respect to *V*. This is analogous to assuming some sort of mapping from the 3D HH (i.e. excluding *m*) to a 2D model, and again we see that coefficients of Eq. (9), with the 3/4 correction factor multiplying *m _{∞}*, are related to the coefficients of Eq. (2)

## References

- Abbott LF, Kepler TB. Model Neurons: From Hodgkin-Huxley to Hopfield. In: Garrido L, editor. Statistical Mechanics of Neural Networks. Berlin: Springer-Verlag; 1990. pp. 5–18.
- Abeles M. Role of the cortical neuron: integrator or coincidence detector? Isr J Med Sci. 1982;18:83–92. [PubMed]
- Aguera y Arcas B, Fairhall AL. What causes a neuron to spike? Neural Comput. 2003;15:1789–1807. [PubMed]
- Aguera y Arcas B, Fairhall AL, Bialek W. Computation in a single neuron: Hodgkin and Huxley revisited. Neural Comput. 2003;15:1715–1749. [PubMed]
- Arsiero M, Luscher HR, Lundstrom BN, Giugliano M. The impact of input fluctuations on the frequency-current relationships of layer 5 pyramidal neurons in the rat medial prefrontal cortex. J Neurosci. 2007;27:3274–3284. [PubMed]
- Benda J, Herz AV. A universal model for spike-frequency adaptation. Neural Comput. 2003;15:2523–2564. [PubMed]
- Bryant HL, Segundo JP. Spike initiation by transmembrane current: a white-noise analysis. J Physiol. 1976;260:279–314. [PMC free article] [PubMed]
- Cantrell AR, Catterall WA. Neuromodulation of Na+ channels: an unexpected form of cellular plasticity. Nat Rev Neurosci. 2001;2:397–407. [PubMed]
- Chance FS, Abbott LF, Reyes AD. Gain modulation from background synaptic input. Neuron. 2002;35:773–782. [PubMed]
- Colbert CM, Magee JC, Hoffman DA, Johnston D. Slow recovery from inactivation of Na+ channels underlies the activity-dependent attenuation of dendritic action potentials in hippocampal CA1 pyramidal neurons. J Neurosci. 1997;17:6512–6521. [PubMed]
- Dayan P, Abbott LF. Theoretical neuroscience: computational and mathematical modeling of neural systems. Cambridge, Mass: Massachusetts Institute of Technology Press; 2001.
- Destexhe A, Pare D. Impact of network activity on the integrative properties of neocortical pyramidal neurons in vivo. J Neurophysiol. 1999;81:1531–1547. [PubMed]
- Destexhe A, Rudolph M, Pare D. The high-conductance state of neocortical neurons in vivo. Nat Rev Neurosci. 2003;4:739–751. [PubMed]
- Destexhe A, Rudolph M, Fellous JM, Sejnowski TJ. Fluctuating synaptic conductances recreate in vivo-like activity in neocortical neurons. Neuroscience. 2001;107:13–24. [PMC free article] [PubMed]
- Ermentrout B. Linearization of F-I curves by adaptation. Neural Comput. 1998;10:1721–1729. [PubMed]
- Fellous JM, Rudolph M, Destexhe A, Sejnowski TJ. Synaptic background noise controls the input/output characteristics of single cells in an in vitro model of in vivo activity. Neuroscience. 2003;122:811–829. [PMC free article] [PubMed]
- Fleidervish IA, Friedman A, Gutnick MJ. Slow inactivation of Na+ current and slow cumulative spike adaptation in mouse and guinea-pig neocortical neurones in slices. J Physiol. 1996;493(Pt 1):83–97. [PMC free article] [PubMed]
- Gerstein GL, Mandelbrot B. Random Walk Models for the Spike Activity of a Single Neuron. Biophys J. 1964;4:41–68. [PMC free article] [PubMed]
- Gerstner W, Kistler WM. Spiking neuron models: single neurons, populations, plasticity. Cambridge, U.K.; New York: Cambridge University Press; 2002.
- Giugliano M, Bove M, Grattarola M. Activity-driven computational strategies of a dynamically regulated integrate-and-fire model neuron. J Comput Neurosci. 1999;7:247–254. [PubMed]
- Goldman MS, Golowasch J, Marder E, Abbott LF. Global structure, robustness, and modulation of neuronal models. J Neurosci. 2001;21:5229–5238. [PubMed]
- Gonsalves B, Paller KA. Neural events that underlie remembering something that never happened. Nat Neurosci. 2000;3:1316–1321. [PubMed]
- Gutkin B, Ermentrout GB, Rudolph M. Spike generating dynamics and the conditions for spike-time precision in cortical neurons. J Comput Neurosci. 2003;15:91–103. [PubMed]
- Higgs MH, Slee SJ, Spain WJ. Diversity of gain modulation by noise in neocortical neurons: regulation by the slow afterhyperpolarization conductance. J Neurosci. 2006;26:8787–8799. [PubMed]
- Hodgkin AL, Huxley AF. A quantitative description of membrane current and its application to conduction and excitation in nerve. Journal of Physiology. 1952;117:500–544. [PMC free article] [PubMed]
- Hong S, Aguera y Arcas B, Fairhall AL. Single neuron computation: from dynamical system to feature detector. Neural Comput In press. [PubMed]
- Izhikevich EM. Dynamical systems in neuroscience: the geometry of excitability and bursting. Cambridge, Mass: MIT Press; 2007.
- Johnston D, Hoffman DA, Colbert CM, Magee JC. Regulation of back-propagating action potentials in hippocampal neurons. Curr Opin Neurobiol. 1999;9:288–292. [PubMed]
- Kepler TB, Abbott LF, Marder E. Reduction of conductance-based neuron models. Biol Cybern. 1992;66:381–387. [PubMed]
- Koch C. Biophysics of computation: information processing in single neurons. New York: Oxford University Press; 1999.
- Konig P, Engel AK, Singer W. Integrator or coincidence detector? The role of the cortical neuron revisited. Trends Neurosci. 1996;19:130–137. [PubMed]
- LeMasson G, Marder E, Abbott LF. Activity-dependent regulation of conductances in model neurons. Science. 1993;259:1915–1917. [PubMed]
- Mainen ZF, Sejnowski TJ. Reliability of spike timing in neocortical neurons. Science. 1995;268:1503–1506. [PubMed]
- Melnick IV, Santos SF, Safronov BV. Mechanism of spike frequency adaptation in substantia gelatinosa neurones of rat. J Physiol. 2004;559:383–395. [PMC free article] [PubMed]
- Miles GB, Dai Y, Brownstone RM. Mechanisms underlying the early phase of spike frequency adaptation in mouse spinal motoneurones. J Physiol. 2005;566:519–532. [PMC free article] [PubMed]
- Moreno R, de la Rocha J, Renart A, Parga N. Response of spiking neurons to correlated inputs. Phys Rev Lett. 2002;89:288101. [PubMed]
- Murray JD. Mathematical biology. 3. New York: Springer; 2002.
- Oertel D. Synaptic responses and electrical properties of cells in brain slices of the mouse anteroventral cochlear nucleus. J Neurosci. 1983;3:2043–2053. [PubMed]
- Prescott SA, Ratte S, De Koninck Y, Sejnowski TJ. Nonlinear interaction between shunting and adaptation controls a switch between integration and coincidence detection in pyramidal neurons. J Neurosci. 2006;26:9084–9097. [PMC free article] [PubMed]
- Rathouz M, Trussell L. Characterization of outward currents in neurons of the avian nucleus magnocellularis. J Neurophysiol. 1998;80:2824–2835. [PubMed]
- Rauch A, La Camera G, Luscher HR, Senn W, Fusi S. Neocortical pyramidal cells respond as integrate-and-fire neurons to in vivo-like input currents. J Neurophysiol. 2003;90:1598–1612. [PubMed]
- Reyes AD, Rubel EW, Spain WJ. Membrane properties underlying the firing of neurons in the avian cochlear nucleus. J Neurosci. 1994;14:5352–5364. [PubMed]
- Reyes AD, Rubel EW, Spain WJ. In vitro analysis of optimal stimuli for phase-locking and time-delayed modulation of firing in avian nucleus laminaris neurons. J Neurosci. 1996;16:993–1007. [PubMed]
- Richardson MJ. Effects of synaptic conductance on the voltage distribution and firing rate of spiking neurons. Phys Rev E Stat Nonlin Soft Matter Phys. 2004;69:051918. [PubMed]
- Richardson MJ, Gerstner W. Synaptic shot noise and conductance fluctuations affect the membrane voltage with equal significance. Neural Comput. 2005;17:923–947. [PubMed]
- Rothman JS, Manis PB. The roles potassium currents play in regulating the electrical activity of ventral cochlear nucleus neurons. J Neurophysiol. 2003;89:3097–3113. [PubMed]
- Roy SA, Alloway KD. Coincidence detection or temporal integration? What the neurons in somatosensory cortex are doing. J Neurosci. 2001;21:2462–2473. [PubMed]
- Rudolph M, Destexhe A. Characterization of subthreshold voltage fluctuations in neuronal membranes. Neural Comput. 2003a;15:2577–2618. [PubMed]
- Rudolph M, Destexhe A. Tuning neocortical pyramidal neurons between integrators and coincidence detectors. J Comput Neurosci. 2003b;14:239–251. [PubMed]
- Shriki O, Hansel D, Sompolinsky H. Rate models for conductance-based cortical neuronal networks. Neural Comput. 2003;15:1809–1841. [PubMed]
- Slee SJ, Higgs MH, Fairhall AL, Spain WJ. Two-dimensional time coding in the auditory brainstem. J Neurosci. 2005;25:9978–9988. [PubMed]
- Strogatz SH. Nonlinear dynamics and Chaos: with applications to physics, biology, chemistry, and engineering. Reading, Mass: Addison-Wesley Pub; 1994.
- Svirskis G, Kotak V, Sanes DH, Rinzel J. Sodium along with low-threshold potassium currents enhance coincidence detection of subthreshold noisy signals in MSO neurons. J Neurophysiol. 2004;91:2465–2473. [PMC free article] [PubMed]
- Taylor AL, Hickey TJ, Prinz AA, Marder E. Structure and visualization of high-dimensional conductance spaces. J Neurophysiol. 2006;96:891–905. [PubMed]
- Trussell LO. Cellular mechanisms for preservation of timing in central auditory pathways. Curr Opin Neurobiol. 1997;7:487–492. [PubMed]
- Tuckwell HC. Introduction to theoretical neurobiology. Cambridge [Cambridgeshire]; New York: Cambridge University Press; 1988.
- Yu Y, Lee TS. Dynamical mechanisms underlying contrast gain control in single neurons. Phys Rev E Stat Nonlin Soft Matter Phys. 2003;68:011901. [PubMed]

## Formats:

- Article |
- PubReader |
- ePub (beta) |
- PDF (1.8M) |
- Citation

- Computation in a single neuron: Hodgkin and Huxley revisited.[Neural Comput. 2003]
*Agüera y Arcas B, Fairhall AL, Bialek W.**Neural Comput. 2003 Aug; 15(8):1715-49.* - A parameter-space search algorithm tested on a Hodgkin-Huxley model.[Biol Cybern. 2007]
*Reid MS, Brown EA, DeWeerth SP.**Biol Cybern. 2007 Jun; 96(6):625-34. Epub 2007 May 9.* - Dynamical mechanisms underlying contrast gain control in single neurons.[Phys Rev E Stat Nonlin Soft Matter Phys. 20...]
*Yu Y, Lee TS.**Phys Rev E Stat Nonlin Soft Matter Phys. 2003 Jul; 68(1 Pt 1):011901. Epub 2003 Jul 8.* - The response of cortical neurons to in vivo-like input current: theory and experiment: II. Time-varying and spatially distributed inputs.[Biol Cybern. 2008]
*Giugliano M, La Camera G, Fusi S, Senn W.**Biol Cybern. 2008 Nov; 99(4-5):303-18. Epub 2008 Nov 15.* - Computational exploration of neuron and neural network models in neurobiology.[Methods Mol Biol. 2007]
*Prinz AA.**Methods Mol Biol. 2007; 401:167-79.*

- Intrinsic Neuronal Properties Switch the Mode of Information Transmission in Networks[PLoS Computational Biology. ]
*Gjorgjieva J, Mease RA, Moody WJ, Fairhall AL.**PLoS Computational Biology. 10(12)e1003962* - Volterra dendritic stimulus processors and biophysical spike generators with intrinsic noise sources[Frontiers in Computational Neuroscience. ]
*Lazar AA, Zhou Y.**Frontiers in Computational Neuroscience. 895* - Impact of Neuronal Properties on Network Coding: Roles of Spike Initiation Dynamics and Robust Synchrony Transfer[Neuron. 2013]
*Ratté S, Hong S, De Schutter E, Prescott SA.**Neuron. 2013 Jun 5; 78(5)758-772* - Single neuron firing properties impact correlation-based population coding[The Journal of neuroscience : the official ...]
*Hong S, Ratté S, Prescott SA, De Schutter E.**The Journal of neuroscience : the official journal of the Society for Neuroscience. 2012 Jan 25; 32(4)1413-1428* - Increase in Sodium Conductance Decreases Firing Rate and Gain in Model Neurons.[The Journal of neuroscience : the official ...]
*Kispersky TJ, Caplan J, Marder E.**The Journal of neuroscience : the official journal of the Society for Neuroscience. 2012 Aug 8; 32(32)10995-11004*

- Two computational regimes of a single-compartment neuron separated by a planar b...Two computational regimes of a single-compartment neuron separated by a planar boundary in conductance spaceNIHPA Author Manuscripts. May 2008; 20(5)1239

Your browsing activity is empty.

Activity recording is turned off.

See more...