**Corrections**

1 Jun 2009: (2009) Correction: Divisive Gain Modulation with Dynamic Stimuli in Integrate-and-Fire Neurons. PLoS Comput Biol 5(6): 10.1371/annotation/9c4474f6-e58e-41ea-af4b-090bbb86f474. doi: 10.1371/annotation/9c4474f6-e58e-41ea-af4b-090bbb86f474 | View correction

## Abstract

The modulation of the sensitivity, or gain, of neural responses to input is an important component of neural computation. It has been shown that *divisive* gain modulation of neural responses can result from a stochastic shunting from balanced (mixed excitation and inhibition) background activity. This gain control scheme was developed and explored with static inputs, where the membrane and spike train statistics were stationary in time. However, input statistics, such as the firing rates of pre-synaptic neurons, are often dynamic, varying on timescales comparable to typical membrane time constants. Using a population density approach for integrate-and-fire neurons with dynamic and temporally rich inputs, we find that the same fluctuation-induced divisive gain modulation is operative for dynamic inputs driving nonequilibrium responses. Moreover, the degree of divisive scaling of the dynamic response is quantitatively the same as the steady-state responses—thus, gain modulation via balanced conductance fluctuations generalizes in a straight-forward way to a dynamic setting.

## Author Summary

Many neural computations, including sensory and motor processing, require neurons to control their sensitivity (often termed ‘gain’) to stimuli. One common form of gain manipulation is divisive gain control, where the neural response to a specific stimulus is simply scaled by a constant. Most previous theoretical and experimental work on divisive gain control have assumed input statistics to be constant in time. However, realistic inputs can be highly time-varying, often with time-varying statistics, and divisive gain control remains to be extended to these cases. A widespread mechanism for divisive gain control for static inputs is through an increase in stimulus independent membrane fluctuations. We address the question of whether this divisive gain control scheme is indeed operative for time-varying inputs. Using simplified spiking neuron models, we employ accurate theoretical methods to estimate the dynamic neural response. We find that gain control via membrane fluctuations does indeed extend to the time-varying regime, and moreover, the degree of divisive scaling does not depend on the timescales of the driving input. This significantly increases the relevance of this form of divisive gain control for neural computations where input statistics change in time, as expected during normal sensory and motor behavior.

**Citation: **Ly C, Doiron B (2009) Divisive Gain Modulation with Dynamic Stimuli in Integrate-and-Fire Neurons. PLoS Comput Biol 5(4):
e1000365.
doi:10.1371/journal.pcbi.1000365

**Editor: **Lyle J. Graham, Université Paris Descartes, Centre National de la Recherche Scientifique, France

**Received:** November 14, 2008; **Accepted:** March 18, 2009; **Published:** April 24, 2009

**Copyright:** © 2009 Ly, Doiron. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

**Funding: **CL is supported by National Science Foundation Postdoctoral Fellowship DMS-0703502. BD is supported by National Science Foundation grant DMS-081714. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

**Competing interests:** The authors have declared that no competing interests exist.

### Introduction

Gain modulation (or gain control) is an adjustment of the input-output response of neurons, and is widely observed during neural processing [1]. Gaze direction sets the response gain in primary visual [2], posterior parietal cortex [3], and auditory brainstem [4]. In specific species, gain control mechanisms produce an invariance of receptive field properties [5] and orientation selectivity [6] to changes in overall stimulus contrast. Higher cognitive processes, such as attention, modulate the response gain of cells in primary visual cortex [7], as well as in V4 [8]. Finally, it has recently been shown that gain control schemes are needed to control behavior in invertebrates [9]. Despite the clear importance of gain control in a variety of neural computations, the biophysical mechanisms that support specific gain control mechanisms have been elusive [10]–[20].

Noise induced phenomena in nonlinear systems are a rich avenue of study [21], with recent interest on the impact of fluctuations on excitable systems, such as neurons [22]. Chance et al., Doiron et al., and Hô & Destexhe [11],[16],[23] all report that an increase in the fluctuations of background conductance inputs results in a decrease of the overall gain of the transfer between a static driving input and the mean output firing rate. In particular, if the balance between background excitation and inhibition is carefully controlled [11], then the gain control is purely divisive (or multiplicative). This means that an increase in conductance fluctuations acts to scale the transfer function over a large range of input by a simple constant multiplier (<1). Related work has further explored the impact of fluctuations on spike response [13]–[15],[20],[24],[25], with a the manipulation of the neural transfer function by background fluctuations being a central focus.

These studies address the gain control of a transfer function where the signal is either static or statistically stationary and the neural output is the time averaged firing rate. However, many neural coding tasks involve the processing of time-varying, high frequnecy stimuli. In these situations neural response are often transient, and a quasi-static approximation of input-output transfer fails to capture the actual spike response. For example, in the rodent vibrissa sensory [26], auditory [27]–[29], and electrosensory systems [30] stimuli and responses modulate on the order of a few milliseconds, i.e., on the order of, or even faster, than typical membrane time constants of neurons. Even in the visual system, where the relevant timescales of natural scenes are much slower, the response precision of thalamic neurons is at the millisecond level, and standard static transfer function analysis fails to capture neural response [31], yet contrast induced gain control persists [32]. In this study, we address the question of whether the fluctuation induced gain control mechanism explored for static transfer [11],[16],[23] can be operative for dynamic stimuli as well.

Any theoretical treatment of this problem requires 1) a framework accurately capturing the time varying spike response owing to time varying input statistics (e.g. temporally inhomogeneous input and output statistics), and 2) sufficient biophysical detail to incorporate conductance based synaptic inputs within spike creation. A useful tool for incorporating these two features into neuron models is the population density method [33]–[39]. In particular, Nykamp & Tranchina [35] have developed a simple one-dimensional population density method of conductance based leaky integrate-and-fire models (LIF). The one-dimensional version of the population density method allow us to easily study the firing rate responses to dynamic stimuli in the conductance based formalism of Chance et al. [11]. Minor differences in our proposed model and their dynamic clamp experiments to mimic conductance based inputs are presented in the discussion section. We first show that divisive gain modulation of the steady-state responses only hold for low output firing rates, in particular, where neurons are in the classical subthreshold regime. Second, when restricted to this regime we find the transient responses to dynamic stimuli, which can differ greatly from the quasi-static equilibrium response, also exhibit divisive gain modulation via fluctuation background conductances with the same scaling factor as computed in the static case. Thus, the divisive gain modulation proposed by Chance et al., Doiron et al., and Hô & Destexhe [11],[16],[23] generalizes to the dynamic situation in a very natural way.

### Methods

#### Integrate-and-fire neuron

We consider a leaky integrate-and-fire neuron (LIF) driven by a pre-synaptic population of excitatory (e) and inhibitory (i) cells. The neuron's voltage change is given by a random differential equation:(1)

Dividing by the leakage conductance yields:(2)

where is the membrane time constant, is the random size (for simplicity, chosen from the same distribution) of the excitatory/inhibitory synaptic event. The arrival times of both excitatory and inhibitory synaptic inputs are governed by modulated Poisson processes with mean rates , respectively. Throughout, is the resting membrane voltage, is the excitatory while is the inhibitory reversal potential. When the neuron's voltage crosses , a spike is recorded and the neuron enters a refractory period for a fixed time of , after which, its voltage is reset to . Consequently, the neuron's voltage varies between (). Throughout this paper, we will set , , , , , , and in accordance with estimates from experimental measures. We choose the average value of the random variables so that the neuron's voltage change (from ) is ±0.5 mV [40]. The random variable has a parabolic distribution function with finite support: for and 0 otherwise. It is convenient to define a new random variable , because upon receiving an excitatory synaptic event, the neuron's voltage will increase by (see Nykamp & Tranchina [35] for a derivation). The neuron's voltage will decrease in a similar way upon receiving an inhibitory event: . Thus, satisfy: and .

We decompose the pre-synaptic input into a time-inhomogeneous ‘driver’ term , and time-homogeneous background terms :(3)

The background synaptic activity is *balanced* [11],[40], namely are chosen so that, in the absence of the driver input (), the random target voltage will have mean equal to the resting potential: . This will be true if:(4)

Of interest are the output threshold crossing times, and we estimate response statistics by combining the responses from trials where the arrival times are statistically independent across trials yet share the same generating intensities . The instantaneous firing rate of the neuron is defined as(5)

where is the threshold crossing recorded during trial . Throughout the paper we are interested in the relationship between the driver and the response , and specifically how the balanced activity can modulate the relationship.

Figure 1 is a schematic diagram of the representative leaky integrate-and-fire neuron from the population receiving the combination of driver and balanced inputs. For the sake of exposition, we focus on three different intensities of balanced background inputs: to be 1100 s^{−1}, 1400 s^{−1}, and 1900 s^{−1} (with corresponding , 1361.24 s^{−1}, and 1847.40 s^{−1}, respectively), which we respectively label *low* (black), *medium* (red), and *high* (blue). Chance et al. [11] modified the background level by various rate factors and labeled the regimes 1X, 2X, etc., which is slightly different than our convention of *low*, *medium*, and *high*. However, the resulting steady-state input/output curves (Fig. 2) are similar to those in Chance et al. [11]. Also, our results below hold equally well for many other sets of balanced background activity. For a particular background intensity (low in this case) with random excitatory drive , the output is random (see spike raster plots). As the balanced background activity is increased, the variability in the voltage also increases (Fig. 1B).

**Figure 1. Input-output schematic for population of LIF neurons with a combination of driving input and balanced background fluctuations.**

(A) Excitatory driving input with rate . (B) Balanced fluctuating background inputs with rates . For illustrative purposes the evolution of is shown when ; three intensities of background input are shown. (C) Sample realization of the LIF dynamic. (D) Raster plots of the output spikes are shown (Monte Carlo). (E) The output firing rate , computed by the population density method (see Equations (6)–(8)), is a fast and efficient method for capturing the output firing rate. It matches the average firing rate of 100,000 random LIF neurons computed by Monte Carlo simulation.

doi:10.1371/journal.pcbi.1000365.g001**Figure 2. Gain modulation in the steady state.**

(A) The response curve for different levels of balanced background activity ( is determined once is specified, see Equation (4)). For high output firing rates outside of the boxed region, the slopes of all of the response curves are almost equal. (B) Top Panel: zoomed region of (A). Bottom Panel: a least squares fit was used to find the scalar (see Equation (11)), and we plot the scaled response . Here, and .

doi:10.1371/journal.pcbi.1000365.g002#### Population density approach

A Monte Carlo simulation of Equation (2) would be computationally expensive to ensure an accurate result. In many studies only qualitative effects are reported, and thus quantitative accuracy is not at a premium. However, in our study the accuracy demands are large, as we will quantitatively compare the time dependent for various levels of background intensities. To overcome the errors inherent in finite data from Monte Carlo simulations we use population density methods [35], known to give very accurate estimates of (Fig. 1E) for the idealized neural models described by Equations (2)–(5).

In the population density method, neurons with similar biophysical properties are grouped together, and the evolution of a density function is considered. In brief, describes the voltage probability density over many statistically independent neurons. Integrating the density over a region in state space gives the probability that a neuron randomly chosen from the population will be in that region of state space:(6)

Let denote the probability current; a signed quantity with the convention that positive/negative is the probability per unit time of crossing from below/above. The evolution of is governed by a continuity equation [35]:(7)

We separate the probability current into three distinct terms:

The first term, represents the deterministic leak to rest in the absence of synaptic events. The second and third terms, , model the excitatory and inhibitory synaptic input driving the population. Mathematically we have:

where is the complementary cumulative distribution function: , for . With the chosen distribution for , the functions above are (setting ):

Finally, the instantaneous firing rate, , is the flux of probability current through from below:

(8)

The firing dynamics are implemented by an absorbing boundary condition at spike threshold, , and the source term in Equation (7), modeling membrane reset after a refractory delay. The population average firing rate by the population density method (see Eqs (6)–(8)) is a computationally efficient way of capturing , compared to computationally expensive Monte Carlo simulations.

#### Divisive gain modulation

Gain modulation is typically studied in the equilibrium regime [10],[11],[16], where the driver input is constant in time and the response denotes the equilibrium firing rate as a function of input. A *divisive* gain modulation for satisfies(9)

where is the response of the population with some background activity ‘j’ (for our purposes j = 1 is low, j = 2 is medium, and j = 3 is high background activity) and is a scalar. To measure the divisive gain modulation of a response we fit the scaled response curves to (*low*) by minimizing the mean-squared error :(10)

Finding the that minimizes is easily obtained by orthogonally projecting onto the subspace spanned by :(11)

Because we want the largest possible range for divisive gain modulation, we steadily increase the maximum of until the error in (10) becomes significant (i.e., the scaled curves no longer lie on top of each other). Let that maximum value be .

The nonequilbirum response to a time-varying input is given by Equation (8). We extend divisive gain modulation to the nonequilbrium setting, with the analogous description:(12)

(13)

(14)

The degree of divisive gain modulation in the nonequilibrium setting is determined by how well the time-varying responses scale with one another over a range of . Thus, the scalar is now computed from integrals over , compared to integrals over for the equilibrium case (11).

### Results

#### Divisive gain modulation in the steady state for subthreshold firing rates

We compute the equilibrium input/output relationship, , using the same framework as Chance et al. [11] (section: Integrate-and-fire Neuron), in hopes of first reproducing their results. Using balanced excitation and inhibition to mimic background synaptic activity, we compute for different fixed values of the driving input (Fig. 2). To obtain computationally accurate results in reasonable time we employ population density methods (section: Population Density Approach) to estimate the response . Divisive gain modulation via increases of the background rates occurs in the low firing rate region (boxed region of Fig. 2A). In this regime the neuron response is dominated by input fluctuations rather than any intrinsic spike rhythmicity, thereby replicating the high variability observed in the spike responses in cortical networks [40]. Throughout we refer to this as the *fluctuation driven regime*. In the fluctuation dominated regime the responses can be scaled, in the sense of Equations (10)–(11), to nearly quantitatively match one another (Fig. 2B). This rescaling of the response by background fluctuations qualitatively matches the results presented in [11].

In contrast, for very high output firing rates divisive gain modulation does not occur. The responses are nearly linear with very similar slopes (Fig. 2A), showing only a background activity induced translation of the response (often termed subtractive gain modulation [10]). This region corresponds to a regime where input fluctuations have limited impact and the neuron response is predominately determined by the mean value of the input rates, and we refer to this as *drift dominated regime*. Fluctuation induced divisive gain control restricted to low firing rates is consistent with [16], where simulations of a large-scale compartmental neuron model were used. The insensitively of to input fluctuations at large has also been recorded in pyramidal cells and fast-spiking interneurons [41],[42]. However, the exact where gain manipulation changes from divisive to subtractive (as increases) is difficult to compute and is often model specific [14]. Indeed, there are neurons where the influence of noise persists at high firing rates, such as in layer 5 of rat medial prefrontal cortex [24], however, the biophysical mechanisms that support this effect are absent in the standard LIF model.

In summary, population density methods (section: Population Density Approach) can replicate fluctuation-induced divisive gain modulation of the equilibrium response at low firing rates, previously observed in: simple integrate-and-fire models [14]–[16], simulations of biophysical realistic cell models [16],[20], as well as simulated conductance experiments *in vitro* [11].

#### Divisive gain modulation with dynamic stimuli

We study the influence of background fluctuations on the nonequlibrium response to a highly time-varying excitatory drive. We choose an input rate consisting of sums of sinusoids with various amplitudes, phases, and frequencies to mimic ‘rich’ time varying stimuli (for an example see Fig. 3A). This produces an inhomogeneous Poisson process driver input , resulting in a non-stationary in time stochastic driving current. The response inherits the non-staionarities of and is temporally modulated (Fig. 3B, black curve). Even though the stimulus results in a rather narrow range of response firing rates , it has adequately rich temporal modulation to produce output firing rates that are different than the quasi-static response (Fig. 3B, brown curve), obtained by setting .

**Figure 3. Gain modulation with temporally rich stimuli, and a refractory period.**

(A) The driving input for ranging from {1, 10, 25, 30, 50, 60}s^{−1} and chosen randomly. (B) For the highly varying temporal driving input in (A) the output firing rate for balanced background synaptic input *low* computed using the population density method does not match the quasi-static approximation (brown curve). Inset: plot of shows the absolute value of the difference of and the actual response divided by the arithmetic mean can differ greatly. (C) The firing rate response to driving input in (A) with different balanced background levels. (D) The responses scaled with the same coefficients used in Figure 2C are used here ( and ).

The main result of our study is that fluctuation-induced divisive gain modulation is robust for low to moderate output firing rates in response to dynamic stimuli, despite the complicated dynamics of the leaky integrate-and-fire neuron in the nonequilibrium regime (i.e ). To demonstrate we compute the nonequilibrium responses (, , and ), for the three levels of background activity used for the equilibrium case (low, medium, and high). For larger background activity the overall response is reduced, observed here since for all (Fig. 3C). We compute the dynamical analogue of , (see Equations (11) and (14)) and the scaled response , which quantitatively matches the base response (Fig. 3D). This mimics the results for the equilibrium case (compare Figs. 2B and 3C and 3D). It is, a priori, unexpected that the dynamic response (with timescale and refractory period ) should scale in the same way as the equilibrium response .

Previously, Holt & Koch [10] showed that an increase in membrane shunting without a change in input fluctuation causes a translational shift, rather than division of the equilibrium response curves, which was also verified by Chance et al. [11]. To verify that a pure shunting change cannot result in divisive gain modulation of the nonequilibrium responses (Fig. 3D), we fix the background fluctuation level and driver , but increase the deterministic leakage conductance (Equation 1) to mimic different background synaptic activity (conductance) levels. Equivalently, is replaced with a scaled version: , which has the same mean conductance in the absence of driving input as (). In simulations where the background activity is set by deterministic leak rather than by synaptic conductance fluctuations, the neurons had negligible firing rates because they were unlikely to fire by random chance and did not scale in a divisive manner (not shown). For exposition, we set all of the background fluctuation levels to that of *low* and vary , and hence , to mimic deterministic effects of changing background activity so that there are less fluctuations, but still some amount to induce background firing. The unscaled responses (Fig. 4A) were scaled via a least squares fit (Equation (14)). Not surprisingly, the responses do not scale in a divisive manner (Fig. 4B). Thus, divisive gain modulation in the nonequilibrium regime critically depends on changing the background fluctuation levels. We remark that Chance et al. were in the high conductance state when they verified this whereas our regime has less overall conductance.

**Figure 4. Background fluctuations required for divisive gain modulation.**

(A) The response with the same driver input as before (Fig. 3A), but with increased leakage conductance to mimic various background synaptic activity (conductance) levels in a deterministic way. The balanced background fluctuations levels ()are the same (low) in all 3 curves. The black curve has (same curve in Fig. 3), the red curve has , and the blue curve has . (B) The three responses do not scale in a simple manner. A least squares fit (Equation (14)) was used.

doi:10.1371/journal.pcbi.1000365.g004When the dynamic stimuli are increased so that resulting output firing rates are larger, the neurons no longer exhibit divisive gain modulation. Increasing the overall intensity of the driving input (compare Fig. 5A with Fig. 3A) yields firing rates that are an order of magnitude larger (compare Fig. 5B with Fig. 3C). Increasing the overall background activity reduces the overall response magnitude (Fig. 5B), similar to what is observed in both the equilibrium and nonequlibrium regimes. However, when the response curves are scaled by computed for the low rate case pure divisive gain modulation is not observed for the high rate response. There is no trivial (a time independent ) or natural way to scale the output firing rate curves so that they lie on top of each other. Since divisive gain modulation does not hold in the equilibrium setting for high output firing rates (drift dominated regime), one would expect that it does not hold in the nonequilibrium state. However, both the equilibrium and nonequilibrium states are quite different and we present the failure of fluctuation induced division for the sake of completeness. It is interesting to note that for periods of time when the output firing rates are low, divisive gain modulation appears evident, likely owing to a transient excursion into the fluctuation driven regime.

**Figure 5. Divisive gain modulation does not hold for high intensity input drivers.**

(A) Top Panel: Same stimulus in Figure 3, but magnified to include higher output firing rates. Bottom Panel: The response for different balanced background levels . (B) The three responses do not scale in a simple way.

doi:10.1371/journal.pcbi.1000365.g005In our model, when the driving input rate is low, the population of neurons rarely fire action potentials (i.e., low spontaneous activity). The firing rates in our simulations in this state range from nearly 0 to 3 s^{−1}, depending on the background level of activity. Although extracellular recordings in the cortex suggest the neurons can fire spontaneously at rates larger than 2 s^{−1} [43], such experiments are usually biased towards active neurons. Extracellular recordings by [44] that were unbiased towards responsive neurons suggest that many neurons have low spontaneous firing rates and that only a small fraction of neurons respond ‘well’ to stimuli in unanesthetized animals; this fact was also discussed in [43]. Moreover, calcium imaging experiments of awake and anesthetized rats in layer 2/3 of the cortex show that many neurons have resting firing rates less than 1 s^{−1} [45]. The actual firing rate of neurons in the resting state is a contentious issue, but our results hold for many parameter regimes (see Fig. 6).

**Figure 6. Parameter space where divisive gain modulation extends to the nonequilibrium regime.**

(A) The logarithm of the area (or error) between the time-dependent response curve scaled by the equilibrium scale factor and the curve for many background levels and many driver inputs: . The values on the vertical axis corresponds to a scaling of the driver input used in Figure 3A (see text for details). The two points at and , 1900 s^{−1} marked by stars (*) correspond to the difference in area between the curves in Figure 3D, and the two black circles (•) at , 1900 s^{−1} correspond to the difference in area between the curves in Figure 5B. Any region with colors in the range of orange to blue correspond to parameters where divisive gain modulation persists. (B) The average (unscaled) time-dependent response of the neurons with the same parameters and driver inputs as (A) are plotted on a logarithmic scale. The three stars (*) at are the average firing rates of the unscaled responses in Figure 3C, and the three black circles (•) at are the average firing rates of the unscaled responses in Figure 5A (bottom panel). A logarthmic scale was used to better highlight the variety of values.

Divisive gain modulation with dynamic stimuli is robust in the subthreshold regime (Fig. 6). To illustrate this point, the response with *low* background level to a time-varying driver input and the response to the same driver input with a second level of background activity are computed. We plot the logarithm of the area (or error , see Equation (13)) between the time-dependent response scaled by the equilibrium scale factor and the response:

A logarthmic scale was used (Fig. 6) to better highlight the variety of values. The driver input is scaled as follows:

where is the driver input used previously (see Fig 3A), is the scaling parameter, and is a parameter that insures in positive and not too small. Notice corresponds to the driver input in Fig. 3A, and with corresponds to the driver input in Fig. 5A. The vertical dot-dashed line in black corresponds to 0 error because it is the reference background curve for a given . The two points marked by stars (*) in Fig. 6A at and , 1900 s^{−1} correspond to the difference in area between the curves in Fig. 3D, which is quite small. In fact, for a large region of parameter space, divisive gain modulation holds (any patch that is orange to blue in Fig. 6A). The two black circles (•) in Fig. 6A at and , 1900 s^{−1} correspond to the difference in area between the curves in Fig. 5B. With larger values, the neurons are in the drift dominated regime, and divisive gain modulation no longer holds, as expected (red regions in Fig. 6A).

The average (unscaled) time-dependent response of the neurons with the same parameters and driver inputs as Fig. 6A are plotted in Fig. 6B on a logarithmic scale:

The three stars (*) at are the average firing rates of the unscaled responses in Fig. 3C, and the three black circles (•) at are the average firing rates of the unscaled responses in Fig. 5A (bottom panel). The average firing rate gives a qualitative idea of how large or small the response is as are varied. For example, the average firing rate at the low level is about 2 s^{−1} but the firing rate response can be quite low and as high as 15 s^{−1} (see Fig. 3B). Thus, divisive gain modulation holds for many parameters in a variety of subthreshold regimes.

#### Comparison of optimal scaling factor of equilibrium and nonequlibrium responses

A gain control scheme will be effective in unpredictable environments if it is *quantitatively* insensitive to the timescales of the input, or in other words the degree to which the response is scaled should not depend on the spectral content of the signal. For fluctuation induced gain control we then require that the scaling factor associated with a specific background state would need to be independent of the temporal frequencies in the driver input . To test this we compare the optimal scaling factor between two dynamical responses (each with a distinct balanced background state) where the synaptic driving input is:

Notice the specified varies from 0 to , so that synaptic input rates are non-negative. Let us denote by for two given background rates driven by sinusoidal input with frequency in Hz (here is not the conventional radian frequency). When is in a low range the differences between and are negligible over a wide range of (Fig. 7). This result is robust for a range of background states (Fig. 7A–D). The quantitative match between the divisive scaling of equilibrium and nonequlibrium responses extends to more complicated temporal modulations of the driving input (Fig. 3A). Specifically, we find that for the results shown previously ( and in Figs. 2 and 3). Thus, fluctuation induced gain control is quantitatively insensitive to the timescales of the driving input.

**Figure 7. Optimal scaling factor for sinusoidal input compared with equlibrium scaling factor.**

The red line is the optimal scaling factor (11) of the equilibrium input/output curves computed for , and the black line with dots is the optimal scaling factor (14) of the two dynamical responses with sinusoidal input . The scaling factors match very well for a variety of pairs of balanced background synaptic inputs. Top panels to bottom panels have background synaptic input rates of: (A) , (B) , (C) , (D) . See Equation (4) for corresponding background balance of excitation and inhibition.

doi:10.1371/journal.pcbi.1000365.g007#### Frequency response to weakly time varying inputs

To better describe the mechanism underlying fluctuation-induced divisive gain control in the nonequlibrium, we focus on a weak time modulation of the input drive and compute the linear frequency response [34],[46],[47]. The frequency response function gives the first order temporal modulation of output firing rate assuming the synaptic driving input consists of a large constant component and a small time-varying component:

Here we have set to be some fixed driver synaptic input rate, making the overall time independent excitatory input , while the inhibitory input is still . In total we then have the equilibrium state defined by the triplet , and the time dependent component of the driver simply . Assuming we approximate:(15)

The time modulation of the response is characterized by , indicating how large or small the first order response is to time-varying input of frequency and amplitude . is a complex number with a modulus and phase : .

Our earlier results (Fig. 3) show that for the same driver input and different background inputs that for some scaling factor . However, we know that in limit the equilibrium response also satisfies (Fig. 2). Combining these two results, and neglecting the terms in Equation (15), predicts that where is a background state. Satisfyingly, when neurons are in the fluctuation-dominated regime does indeed multiplicatively scale in the same quantitative manner for different levels of balanced background synaptic input scale (Fig. 8A and 8B). The phase component is the same for all and tested (insert Fig. 8A) and hence can not change the response for different . Thus from the quantitative scaling match of both and we expect fluctuation-induced divisive gain control to extend to weak inputs.

**Figure 8. The frequency response in the fluctuation and drift dominated regimes.**

(A) Fluctuation driven regime. Top Panel: the frequency response is flat up to very large frequencies for all 3 different levels of balanced background activity. In all 3 cases, there was a constant excitatory super-imposed on top of various balanced background inputs: *low*, *medium*, and *high*. Bottom Panel: the frequency responses for the 3 different levels of balanced background activity are scaled the same multiplicative factor ( in Figs. 2 and 3) for a large range of frequencies. (B) Drift dominated regime. Top Panel: the frequency response for 3 levels of balanced background activity with a constant excitatory super-imposed on top of various balanced background inputs: low, medium and high. Bottom Panel: the frequency responses do not scale in a multiplicative manner.

We remark that the near exact scaling of in the high frequency range () is important; if the multiplicative scaling was only true in the flat region of () then fluctuation-induced divisive gain control would fail in the nonequlibrium, i.e. when the quasi-static approximation fails. To be more specific, , if we neglect the fluctuations given by the driver Poisson process. Thus the scaling of for is completely explained by the scaling of the gain of . However, multiplicative scaling for ensures that fluctuation induced gain control will extend into the nonequilibrium regime, even though the quasi-static approximation fails.

When the neurons are in the drift dominated regime, the frequency responses does not scale in a multiplicative manner because there are resonant peaks at integer multiples of the steady-state firing rate [34],[48],[49], and these resonant peaks occur at different frequencies for various balanced background synaptic activity (see Fig. 5B). Thus, divisive gain modulation with dynamic stimuli cannot possibly occur. The frequency responses in the drift dominated regime are scalar multiples of each other up to 10 Hz, where there appears to be divisive gain modulation with the same equilibrium scaling factors (see Fig. 5B). As explained in the previous paragraph, frequency response for is equal to the frequency response for . However, the multiplicative scaling breaks down for the same range where the quasi-static approximation breaks down, meaning that for drift dominated responses any fluctuation induced gain control in the equilibrium regime will not transfer to the nonequilibrium response.

### Discussion

Chance et al. [11] described a mechanism by which divisive gain modulation results from a balanced, fluctuating background synaptic activity which both shunts and linearizes the membrane to spike transfer. The response is a scaled version of a baseline condition , and the dividing factor is independent of the driver intensity . However, many stimuli induce input and output statistics which vary on the timescale of neural integration [26],[27],[30],[31]. Extending fluctuation induced gain control to accurately divide the response to these inputs is not automatic, as the spike-reset and refractory dynamics significantly shape the response in the nonequilibrium regime to be significantly different than the quasi-static approximation. However, our results show that the fluctuation induced gain control does extend to the nonequilibrium regime, increasing the potential utility of this form of gain control in neural processing. Furthermore, establishing the independence of the scaling term from the timescale of the driver greatly simplifies the circuitry required to implement gain control. In its simplest scenario, the gain of the response is set by the background rates which maintain their scaling effect despite processing unpredictable environments where inputs statistics can vary dramatically.

The analysis of the time dependent response for weak signals showed how a scaling of is inherited from an equivalent scaling of and the response function by fluctuating background conductances. The response to an input of arbitrary strength and spectrum can be written using the Volterra expansion [50]:

where is the inverse Fourier transform of the response function described in Equation (15). Fluctuation induced gain control extends well into the nonlinear regime, evidenced by the empirical agreement in regimes where varies significantly about (Fig. 3D). In this case, the influence of the higher order terms in the Volterra expansion are likely important. We conjecture that, within the fluctuation dominated regime, each response function , meaning that the multiplicative scaling extends, response function-by-response function, analogously into the nonlinear regime. This scenario is opposed to the one where each term exhibits scaling with distinct terms, yet the sum of terms somehow scales with , forcing agreement with our results where has large temporal variance (Fig. 3D). In principle computing is quite difficult, however, if this scaling is correct then the influence of the stochastic background on , in the fluctuation driven regime, becomes straightforward.

Divisive gain control is a central tool in many neural computations [1], yet robust biophysical mechanisms that produce gain control are elusive [10]–[13],[16]. Our work gives further evidence that using background fluctuations as a mechanism to scale responses is a surprisingly stable mechanism operable for a variety of input statistics. Fluctuation induced effects on the equilibrium state transfer different from divisive gain control have been reported [24],[25]. Notably, [24] have shown that the firing response of pyramidal cells in layer 5 is sensitive to fluctuations at high rates, where the mean current no longer determines the spike rate. The mechanisms responsible are not present in the standard LIF model, however, modifications could possibly be made to model these effects and a population density equation could, in principle, be derived. These models would require more state variables and/or equations and in general are not computationally tractable without some reduction or approximation. Sophisticated methods for other neuron models have been developed [51]–[53]. Extending gain control to nonequilibrium responses to a larger class of models is currently an open avenue of research.

The LIF model we have used is an approximation to the dynamic clamp experiments of Chance et al. [11]. One difference is that our model does not have temporal correlations in the synaptic conductances, while there are temporal correlations in the experiments even though Chance et al. average over time (and trials) to obtain the firing rate. Also, we are using a simple yet biophysical spiking neuron model, where the level of background activity determines the variance of the background voltage (see Fig. 1B), consistent with the observations that membrane potential variability changes with the internal brain state [54]. In Chance et al. the variance of background voltage was the same for all background fluctuation levels, ensuring that the variability of the output firing rate is constant. Despite these differences, our results suggest that fluctuation induced divisive gain modulation is viable with dynamic stimuli.

The population density equations (6)–(8) that characterize the LIF model contain a partial differential-integral equation that is difficult to analyze. Our model is more general than white noise models that have an advection/diffusion density equation (e.g, Fokker-Planck equation) because it allows for large voltage changes upon receiving synaptic input events. However, the simulations shown in this paper are in the regime where the diffusion approximation is good. If the voltage change upon receiving synaptic events (excitatory or inhibitory) is assumed to be small, a good diffusion approximation of (6)–(8) is obtained by replacing with in the integrals in the probability current terms and (see Text S1 and Figure S1). With large voltage changes, a similar approximation can be obtained by a re-scaling of the equation around the (deterministic) mean. However, a direct comparison to the Fokker-Planck equation with white noise conductances still must be done numerically because of the conductance-based input (Text S1 outlines the Fokker-Planck approximation to the full density equation and Figure S1 shows the magnitude of the advection/diffusion coefficients). Moreover, the analytic formulas obtained with advection/diffusion equations are often computed numerically and usually assume at least a quasi-static approximation. With Poisson current injection however, a closed form Fokker-Planck approximation is obtained with drift and diffusion coefficients that can be written exactly in terms of voltage, input rates, and the statistics of . An analytical explanation of the robust scaling of the firing rate responses that is observed remains elusive yet is conceivable because of the many analytical results obtained for density equations of a variety of neuron models [51],[52]. However, we remark that even in the equilibrium regime an analytic explanation of divisive gain modulation via conductance fluctuations is difficult to obtain [14].

### Supporting Information

The advection/diffusion coefficients. (A) The functions d^{e/i}_{0}(v). (B) The functions d^{e/i}_{1}(v). Parameters: PSP = +0.5 or −0.5 mV (see main text for an explanation), τ_{m} = 20 ms, ε_{i} = −80 mV, ε_{r} = −70 mV, V_{th} = −55 mV, ε_{e} = 0 mV.

doi:10.1371/journal.pcbi.1000365.s001

(8.28 MB TIF)

Fokker-Planck approximation to full density equations

doi:10.1371/journal.pcbi.1000365.s002

(0.01 MB TEX)

### Acknowledgments

This work was started at the Courant Institute of Mathematical Sciences at NYU (CL & BD), and the Center for Neural Science at NYU (BD). We thank Alex Reyes, Anne-Marie Oswald, and Dan Tranchina for fruitful discussions. BD thanks Jessica Cardin for a motivating discussion.

### References

- 1. Salinas E, Thier P (2000) Gain modulation: a major computation principle of the central nervous system. Neuron 27: 15–21.
- 2. Trotter Y, Celebrini S (1999) Gaze direction controls response gain in primary visual-cortex neurons. Nature 398: 239–242.
- 3. Brotchie P, Andersen R, Snyder L, Goodman S (1995) Head position signals used by parietal neurons to encode locations of visual stimuli. Nature 375: 232–235.
- 4. Winkowski D, Knudsen E (2006) Top-down gain control of the auditory space map by gaze control circuitry in the barn owl. Nature 439: 336–339.
- 5. Alitto H, Usrey W (2004) Influence of contrast on orientation and temporal frequency tuning in ferret primary visual cortex. J Neurophysiol 91: 2797–2808.
- 6. Ferster D, Miller K (2000) Neural mechanisms of orientation selectivity in the visual cortex. Annu Rev Neurosci 23: 441–471.
- 7. McAdams C, Reid R (2005) Attention modulates the responses of simple cells in monkey primary visual cortex. J Neurosci 25: 11023–11033.
- 8. McAdams C, Maunsell J (1999) Effects of attention on orientation tuning functions of single neurons in macaque cortical area v4. J Neurosci 19: 431–441.
- 9. Baca S, Marin-Burgin A, Wagenaar D, Kristan WB (2008) Widespread inhibition proportional to excitation controls the gain of a leech behavioral circuit. Neuron 57: 276–289.
- 10. Holt G, Koch C (1997) Shunting inhibition does not have a divisive effect on firing rates. Neural Comput 9: 1001–1013.
- 11. Chance F, Abbott L, Reyes A (2002) Gain modulation from background synaptic input. Neuron 35: 773–782.
- 12. Mehaffey W, Doiron B, Maler L, Turner R (2005) Deterministic multiplicative gain control with active dendrites. J Neurosci 25: 9968–9977.
- 13. Mitchell S, Silver R (2003) Shunting inhibition modulates neuronal gain during synaptic excitation. Neuron 38: 433–445.
- 14. Burkitt A, Meffin H, Grayden D (2003) Study of neuronal gain in conductance-based leaky integrate and fire neuron model with balanced excitatory and inhibitory synaptic input. Biol Cybern 89: 119–125.
- 15. Longtin A, Doiron B, Bulsara A (2002) Noise-induced divisive gain control in neuron models. BioSystems 67: 147–156.
- 16. Doiron B, Longtin A, Berman N, Maler L (2001) Subtractive and divisive inhibition: effect of voltage-dependent inhibitory conductances and noise. Neural Comput 13: 227–248.
- 17. Salinas E, Abbott L (1997) Invariant visual perception from attentional gain fields. J Neurophysiol 77: 3267–3272.
- 18. Abbott L, Varela J, Sen K, Nelson S (1997) Synaptic depression and cortical gain control. Science 275: 220–223.
- 19. Cardin JA, Palmer L, Contreras D (2008) Cellular mechanisms underlying stimulus-dependent gain modulation in primary visual cortex neurons in vivo. Neuron 59: 150–160.
- 20. Prescott S, De Koninck Y (2003) Gain control of firing rate by shunting inhibition: roles of synaptic noise and dendritic saturation. Proc Natl Acad Sci U S A 100: 2076–2081.
- 21.
Haken H (2004) Synergetics: Introduction and Advanced Topics. Springer. pp. 229–326. Chapters 8–10.
- 22. Lindner B, García-Ojalvo J, Neiman A, Schimansky-Geier L (2004) Effects of noise in excitable systems. Phys Rep 392: 321–427.
- 23. Hô N, Destexhe A (2000) Synaptic background activity enhances the responsiveness of neocortical pyramidal neurons. J Neurophysiol 84: 1488–1496.
- 24. Arsiero M, Luscher HR, Lundstrom BN, Giugliano M (2007) The impact of input fluctuations on the frequency-current relationships of layer 5 pyramidal neurons in the rat medial prefrontal cortex. J Neurosci 27: 3274–3284.
- 25. Higgs M, Slee S, Spain W (2007) Diversity of gain modulation by noise in neocortical neurons: Regulation by the slow afterhyperpolarization conductance. J Neurosci 26: 8787–8799.
- 26. Ritt J, Andermann M, Moore C (2008) Embodied information processing: Vibrissa mechanics and texture features shape micromotions in actively sensing rats. Neuron 57: 599–613.
- 27. Grothe B, Klump G (2000) Temporal processing in sensory systems. Curr Opin Neurobiol 10: 467–473.
- 28. Köppl C (1997) Phase locking to high frequencies in the auditory nerve and cochlear nucleus magnocellularis of the barn owl, Tyto alba. J Neurosci 17: 3312–3321.
- 29. Mason A, Oshinsky M, Hoy R (2001) Hyperacute directional hearing in a microscale auditory system. Nature 410: 686–690.
- 30. Benda J, Lonftin A, Maler L (2006) A synchronization-desynchronization code for natural communication signals. Neuron 52: 347–358.
- 31. Butts D, Weng C, Jin J, Yeh CI, Lesica N, et al. (2007) Temporal precision in the neural code and the timescales of natural vision. Nature 449: 92–95.
- 32. Lesica N, Jin J, Weng C, Yeh CI, Butts DA, et al. (2007) Adaptation to stimulus contrast and correlations during natural visual stimulation. Neuron 55: 479–491.
- 33. Knight BW, Omurtag A, Sirovich L (2000) The approach of a neuron population firing rate to a new equilibrium: an exact theoretical result. Neural Comput 12: 1045–1055.
- 34. Knight BW (2000) Dynamics of encoding in neuron populations: some general mathematical features. Neural Comput 12: 473–518.
- 35. Nykamp DQ, Tranchina D (2000) A population density approach that facilitates large-scale modeling of neural networks: analysis and an application to orientation tuning. J Comput Neurosci 8: 19–50.
- 36. Haskell E, Nykamp DQ, Tranchina D (2001) Population density methods for large-scale modeling of neuronal networks with realistic synaptic kinetics: cutting the dimension down to size. Network 12: 141–174.
- 37. Fourcaud N, Brunel N (2002) Dynamics of the firing probability of noisy integrate-and-fire neuron. Neural Comput 14: 2057–2110.
- 38. Richardson M (2004) Effects of synaptic conductance on the voltage distribution and firing rate of spiking neurons. Phys Rev E 69: 051918.
- 39. Apfaltrer F, Ly C, Tranchina D (2006) Population density methods for stochastic neurons with a 2-D state space: application to neural networks with realistic synaptic kinetics. Network 17: 373–418.
- 40. Shadlen MN, Newsome WT (1998) The variable discharge of cortical neurons: implications for connectivity, computation, and information coding. J Neurosci 18: 3870–3896.
- 41. Rauch A, LaCamera G, Lüscher H, Senn W, Fusi S (2003) Neocortical pyramidal cells respond as integrate-and-fire neurons to in vivo-like currents. J Neurophysiol 90: 1598–1612.
- 42. LaCamera G, Rauch A, Thurbon D, Lüscher H, Senn W, et al. (2006) Multiple time scales of temporal response in pyramidal and fast spiking cortical neurons. J Neurophysiol 96: 3448–3464.
- 43. Sanchez-Vives M, Descalzo V, Reig R, Figueroa N, Compte A, et al. (2008) Rhythmic spontaneous activity in the piriform cortex. Cereb Cortex 18: 1179–1192.
- 44. Hromádka T, DeWeese M, Zador A (2008) Sparse representation of sounds in the unanesthetized auditory cortex. PLoS Biol 6: e16. doi:10.1371/journal.pbio.0060016.
- 45. Greenberg D, Houweling A, Kerr J (2008) Population imaging of ongoing neuronal activity in the visual cortex of awake rats. Nat Neurosci 11: 749–751.
- 46.
Risken H (1989) The Fokker-Planck equation. 2nd Ed. Berlin: Springer-Verlag. pp. 163–178.
- 47. Richardson M (2007) Firing-rate response of linear and nonlinear integrate-and-fire neurons to modulated current-based and conductance-based synaptic drive. Phys Rev E 76: 021919.
- 48. Knight BW (1972) Dynamics of encoding in a population of neurons. J Gen Phys 59: 734–766.
- 49. Knight BW (1972) The relationship between the firing rate of a single neuron and the level of activity in a population of neurons. Experimental evidence for resonant enhancement in the population response. J Gen Phys 59: 767–778.
- 50.
Dayan P, Abbott L (2001) Theoretical Neuroscience: Computational and Mathematical Modeling of Neural Systems. Cambridge, MA: MIT Press. pp. 45–86.
- 51. Chizhov A, Graham L (2007) Population model of hippocampal pyramidal neurons, linking a refractory density approach to conductance-based neurons. Phys Rev E 75: 011924.
- 52. Chizhov A, Graham L (2008) Efficient evaluation of neuron populations receiving colored-noise current based on a refractory density method. Phys Rev E 77: 011910.
- 53. Ly C, Tranchina D (2009) Spike train statistics and dynamics with synaptic input from any renewal process: a popuation density approach. Neural Comput 21: 360–396.
- 54. Poulet J, Petersen C (2008) Internal brain state regulates membrane potential synchrony in barrel cortex of behaving mice. Nature 454: 881–885.

## Comments

Alternative version of Figure 3

Posted by PLoS_CompBiol

PDF version of Text S1

Posted by PLoS_CompBiol

Update to email address

Posted by PLoS_CompBiol