Abstract
Recently, deep learning algorithms have outperformed human experts in various tasks across several domains; however, their characteristics are distant from current knowledge of neuroscience. The simulation results of biological learning algorithms presented herein outperform stateoftheart optimal learning curves in supervised learning of feedforward networks. The biological learning algorithms comprise asynchronous input signals with decaying input summation, weights adaptation, and multiple outputs for an input signal. In particular, the generalization error for such biological perceptrons decreases rapidly with increasing number of examples, and it is independent of the size of the input. This is achieved using either synaptic learning, or solely through dendritic adaptation with a mechanism of swinging between reflecting boundaries, without learning steps. The proposed biological learning algorithms outperform the optimal scaling of the learning curve in a traditional perceptron. It also results in a considerable robustness to disparity between weights of two networks with very similar outputs in biological supervised learning scenarios. The simulation results indicate the potency of neurobiological mechanisms and open opportunities for developing a superior class of deep learning algorithms.
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Introduction
A primary objective of artificial learning algorithms is to pinpoint and classify the many objects that compose an event based on their relative timings. A commonly used strategy is to reduce the complexity of such an event to synchronous inputs, and analyze it using feedforward networks^{1,2,3,4,5,6} (Fig. 1A, left). In literature, this strategy has been extensively evaluated using rulebased statistical physics and nonlinear dynamics methods^{7,8,9,10,11,12,13,14,15,16,17,18,19,20}.
Unlike modern computers^{21}, the dynamics of the brain do not comply with a welldefined global clock^{22,23,24}, which is a characteristic of physical systems that obey random sequential updating. Hence, the biological scheme must cope with asynchronous inputs^{21,25} (Fig. 1A, right). This objective is achieved using decaying input summation and the spiketimingdependentplasticity (STDP)^{26,27} mechanism. In STDP, a weight that induces a subthreshold signal on a neuron is weakened or strengthened based on its relative timing to adjacent spikes, generated by the same neuron (Fig. 1B). However, the weights that induce abovethreshold signals, i.e. spikes, do not undergo adaptation. Moreover, the biological asynchronous scheme allows multiple outputs for a given input (Fig. 1C, left), as well as different outputs for different timings of the same asynchronous input (Fig. 1C, right). These features (Fig. 1), for instance, are unique to the biological scheme and cannot be realized by its synchronous version.
Although asynchronous inputs contain more information than their synchronous counterparts, they require a practical mechanism that can utilize the timing information contained in the input units (Fig. 1). While biological adaptation considers asynchronous inputs, its quantitative effect on the learning rate is still unclear. Hence, it is fair to conclude that the current concept of biological adaptation stemming from asynchronous inputs^{26,28} has been developed with limited influence^{25,29,30,31} on the current advanced deep learning algorithms^{1,2,3,4,5,6}.
In essence, the brain is a complex network containing billions of nodes (neurons), where each node communicates simultaneously with thousands of other nodes via their links (synapses). However, each node integrates its incoming signals through several long ramified “terminals”, dendritic trees. Recently, a new type of a cooperative nonlinear dynamics was proposed, wherein the adaptation is attributed solely to the several nodal terminals^{32}, instead of the network links. This dendritic adaptation presents a selfcontrolled mechanism to prevent divergence or vanishing of the adaptive parameters in the biological scheme, as opposed to the trend of synaptic plasticity, adaptive links. In addition, it supports selfoscillations of the effective adaptive parameters^{32}. However, the learning capabilities of such cooperative nonlinear dynamics are not fully known; this is in contrast to the extensive literature available on the learning capabilities of existing deep learning algorithms^{1,2,3,4,5,6}.
This work sets out to demonstrate that, compared with the existing artificial intelligence algorithms, asynchronous input based biological learning schemes can improve the scaling of learning rates of feedforward networks. We also show that the generalization error in supervised learning of multilayer feedforward networks is independent of the size of the input, and rapidly decreases with the number of examples.
First, the biological adaptation mechanism for asynchronous inputs, which is similar to STDP, and the phenomenon of decaying input summation are described. Then, using largescale simulations, the generalization error for such biological perceptrons under synaptic plasticity is estimated. The simulation results indicate fast learning rates where the generalization error rapidly decreases with increasing number of examples, independent of the size of the input.
Next, we explore dendritic adaptation, which is based on a new mechanism of swinging between reflecting boundaries of the timedependent dendritic strengths. The results suggest that faster learning rates can be achieved with dendritic adaptation in comparison to a traditional synchronous perceptron. In addition, an extension of the fast learning rates to multilayer networks is also discussed. The paper concludes with guidelines for fundamental questions in the future regarding the development of advanced classes of deep learning algorithms.
Results
Let us consider a scenario where a biological perceptron performs supervised learning^{17,33} (Fig. 2A). In general terms, the objective of a student is to imitate the response of the teacher, where both the student and the teacher have the same architecture^{34}, comprising Ν asynchronous input units, and are characterized by the dynamics of synaptic plasticity (Fig. 1B). The teacher is initially defined by a set of Ν weights, \(\{{w}_{m}\}\), where its leaky integrateandfire (LIF) output neuron^{35} is updated following a serial representation of p examples, i.e., asynchronous inputs (Methods). Thus, each example is said to contain Ν randomly ordered presynaptic spikes, one for each input unit (Fig. 1C, left) resulting in decaying summation by the output unit (Methods), which produces a set of spikes timings for each example. Next, synaptic adaptation is implemented using a version of STDP, for each stimulated weight, which does not result in an evoked spike
Here, \({w}_{m}^{+}\) indicates the updated m^{th} weight and \(\delta (t)\) indicates the strengthening/weakening of a weight conditioned to a prior/later evoked spike at a time delay \(t\) in a given time window (Methods and Fig. S1).
The information provided to the student for each example is the input and the timings of evoked spikes of the teacher (Fig. 2A). For each example, the dynamics of the student consist of the following three steps. First, the outputs are produced and its weights are adapted according to the STDP of the teacher. Note that very similar qualitative results were obtained where the student performs the STDP following the student’s outputs instead of the teacher’s outputs (Fig. S2). Then, learning is performed, wherein the weights with conflicting outputs between the teacher and the student are modified towards an expected agreement (Fig. 2A, right). This learning rule is similar to the traditional synchronous perceptron learning step and can be seen as minimization of a cost function (Methods)
where \({O}_{m}^{T}\) and \({O}_{m}^{S}\) indicate the output of the teacher and the student at the time of the m^{th} input, respectively; \({\rm{\lambda }}\) denotes the learning step size, and \({x}_{m}\) stands for the input amplitude of \({w}_{m}\). The simulation results for various input sizes, Ν, indicate that the generalization error, ε_{g}, scales with p, independent of Ν (Fig. 2B). This extremely fast scaling for the learning rates is compared with the traditional, much slower, optimal learning rate^{17,18}, ε_{g} ∝ 1/α, for the synchronous perceptron, where α = p/Ν. Its underlying dynamical mechanism is suggested by a crossover from ε_{g} ∝ p^{−ϕ}, ϕ > 1, to a slow learning phase where ϕ \(\approx \) 1 (Fig. 2B). In the first phase, the subthreshold weights dominate the dynamics, and most of the output spikes are due to the temporal summation of several temporally consecutive subthreshold inputs (Fig. 2C). Consequently, a fraction of abovethreshold weights was found to be identical for both the teacher and the student (Fig. 2D), which from now on their evoked spikes do not contribute to the learning process, as suggested by Eq. (2). Thus, the learning process is now dominated by low probability events of conflicting outputs, emerging from temporal summation of stimulations of weak weights (Fig. 2D). The probability of finding several weak stimulations consecutively is low; moreover, the weak weights are very similar for both the teacher and the student (Fig. 2D), which significantly reduces the learning rate (Fig. 2B).
In addition to accelerated learning rates, which scale with p, biological learning also exhibits robustness of ε_{g} for a dissimilarity between the weights of the student and the teacher in the late stage of the dynamics (Fig. 2E). For the synchronous perceptron scheme, ε_{g} is a function of the normalized overlap, R (Methods), between the weights of the teacher and the student^{17} (gray line in Fig. 2E), which is eliminated only when the weights are identical, i.e., R = 1. However, for the biological scheme, the dynamical effect of abovethreshold weights is independent of their exact values. In addition, the resetting of the membrane potential after their spikes (Methods) reduces the probability for temporal summation of several weak stimulations. Note that the temporal firing of the biological perceptron is very sensitive to the decaying summation of the membrane potential as well as its reset after firing. Those features result in enhanced ε_{g} of the biological learning at the initial learning stage, small p, in comparison to the synchronous perceptron.
Recently, several experimental and theoretical studies have suggested that dendritic adaptation is a paradigm shift in brain learning^{32}, as opposed to learning based solely on slow synaptic plasticity. The adaptation process in the form of STDP is attributed to \({J}_{i}\), which indicates the strengths of the terminals (dendrites) of the neuron^{36}; the weights, \({w}_{m}\), are timeindependent (Fig. 3A and Methods). This is representative of nonlocal adaptation, where many incoming weights, \({w}_{m}\), to the same terminal (dendrite) concurrently undergo the same adaptation. In the new paradigm, the network dynamics is now counterintuitively governed by the weak \({w}_{m}\), which were previously assumed insignificant. Thus, a novel selfcontrolled mechanism is presented to prevent divergence or vanishing of the learning parameters, as opposed to synaptic adaptation (Figs 2D and S3); the new paradigm also supports selfoscillations of the adaptive parameters, \({J}_{i}\) (Fig. S4).
The supervised learning process of the student under dendritic adaptation, following the teacher and without learning steps, indicates that ε_{g} decays with p, and is independent of the size of the input, Ν (Fig. 3B). In addition, after a considerable decay, ε_{g} jumps to zero at p, which slightly increases with Ν (Fig. 3B). This type of learning with adaptation is a consequence of the temporal oscillating nature of \({J}_{i}\) (Figs 3C and S4); conversely, \({w}_{m}\) converge to extreme values under synaptic plasticity (Figs 2D and S3). Hits at the boundary values form the underlying mechanism for tracking between the strengths of the oscillating \({J}_{i}\) of the teacher and the student (Fig. S5 and Methods). Each hit of a given \({J}_{i}\) decreases its gap between the teacher and the student, because both increase or decrease their strengths simultaneously^{37}. The synchronization of the last \({J}_{i}\) eliminates ε_{g}, which occurs at p that slightly increases with Ν, as it takes more time to synchronize more random walkers (although not independently) with reflecting boundaries^{38}.
For the case of dendritic adaptation, it is likely that during the dynamics a small fraction of the dendritic strengths will become dynamically frozen (Fig. 3D,E). A frozen dendritic strength emerges when all its effective weights, \({w}_{m}\cdot {J}_{i}\), are abovethreshold, i.e. evoke spike for every stimulation; hence its adaptation is terminated. Therefore, the tracking of these frozen dendritic strengths by the student is terminated, those events are reflected by a plateau in ε_{g}; however, the addition of learning steps for \({J}_{i}\) (similar to Eq. (2)) results in a fast decrease of ε_{g} (Fig. 3D, inset). For a learning step size ∝ 1/Ν, ε_{g} scales with α^{−ϕ}; ϕ can increase beyond 1 (Fig. 3D,E), which is defined as scaling for the optimal learning rate for the synchronous perceptron. For a fixed learning step size, independent of the size of the input, ε_{g} scales with p (Fig. S6), similar to the initial scaling of synaptic learning rates (Fig. 2B), however, with a final jump to ε_{g} = 0. The learning process enables the student to track the strengths of the frozen \({J}_{i}\); hence, it scales with α for Ο(1/Ν) learning step size and with p for finite step size.
Dendritic learning also exemplifies the robustness of ε_{g} to a dissimilarity between the weights of the teacher and the student along the dynamics (Fig. 3F). In the initial adaptation process (α \(\lesssim \) 0.2 in Fig. 3F), oscillating \({J}_{i}\) are mainly synchronized by hits at their boundary values, and ε_{g} is mainly a function of the normalized overlap, R, between the weights of the teacher and the student. In the rest of the dynamics, the small fraction of frozen \({J}_{i}\) is learned by the student until ε_{g} is eliminated; however, their exact abovethreshold values are irrelevant (Fig. S7).
Preliminary results indicate that similar qualitative trends are also valid for other multilayer networks with one hidden layer in the synaptic scenario. In particular, the network consists of an input layer which was fully connected to a hidden layer; each layer comprised N units, and a single output unit (Fig. 4). All hidden units and the output unit functioned as LIF neurons (Methods). The results suggest that the generalization error, ε_{g}, scales with the number of examples, and it is independent of the size of the input. In addition, preliminary results indicate that the qualitative conclusions reported here for the dendritic scenario are applicable also for multilayer networks, which, however, deserve further research.
Discussion
In this work, we demonstrate that learning rates of stateoftheart artificial learning algorithms can be improved by adopting fundamental principles that govern the dynamics of the brain. The theory of supervised learning in feedforward networks trained by random examples, suggests that the optimal generalization error scales as \(1/\alpha \,\), where \(\alpha \) is the ratio between the number of examples and the number of input units. This scaling is valid for online as well as for offline learning and is based on synchronous inputs. In other words, all the input units of the feedforward network are stimulated simultaneously, and all delays are equal. The brain essentially analyses complex data, which is abundant in life, using very slow and noisy asynchronous dynamics^{39}. The objective of supervised learning in such an environment appears much more complex and difficult when compared with the synchronous version, even though these asynchronous inputs contain more information about the relative timings of stimulations arriving from different input units. Despite the apparent complexity, the demonstrated biological learning rates outperform the existing artificial ones, where the generalization error decays with the number of examples, and it is independent of the number of input units. For adaptive weights (synaptic plasticity), in addition to biological adaptation (STDP), these fast learning rates can be achieved using learning steps. However, for the new type of cooperative dynamics, dendritic adaptation, the fast decay of the generalization error is achieved only by using adaptation, without the learning steps. The new type of cooperative dynamics is based on a new mechanism of swinging between reflecting boundaries for the timedependent dendritic strengths. Herein, hits at the boundaries result in attractive steps between the teacher and the student networks and provide an example for adaptation as a learning mechanism.
The realization of asynchronous inputs in artificial systems using the synaptic scenario is on the one hand more complex, since the dynamics consist of adaptation and learning, whereas in synchronous inputs scenario only learning steps take place. On the other hand, a learning step for synchronous input scenario requires the update of all weights, whereas for the asynchronous case only a weight with mismatch output is updated, and in addition the adaptation is implemented only for neighboring weights in a defined time window. A similar tradeoff holds for the implementation of supervised learning in multilayer networks and the question which method, synchronous or asynchronous inputs, is more timeconsuming depends on the detailed architecture and dynamical rules.
For the dendritic scenario, the number of tunable parameters is much smaller compared to the synaptic scenario. For instance, the number of tunable parameters between the input and the hidden unit in a multilayer network with one hidden layer (Fig. 4) is N^{2} for the synaptic case and equals to [number of dendrites * N] for a similar dendritic network, where N is the number of input units and hidden units. Hence, the implementation of learning in the dendritic scenario is characterized by a reduced timeconsumption in comparison to its similar synchronous inputs version as well as to its asynchronous synaptic version.
The framework of dendritic adaptation results in timedependent dendritic strengths even for the teacher network; hence, a change in the working premise  from a static teacher to a dynamic teacher  is required. The time separation between training and generalization procedures, which is simple to utilize in the analysis of supervised learning of artificial networks, is invalid in the biological scenario. The theoretical analysis of such a biological reality requires the development of new methods and tools. In addition, the reproducibility of the activity of such networks, i.e. inputoutput relations, on long time scales has to be examined. Given that the network adaptive parameters are timedependent, the same input is expected to produce different outputs for significant separated timings. This may be attributed to the large number of intermediate inputs and adaptation steps. Therefore, such a scenario might require reconsideration of the basic definitions of quantities such as capacity and learning a rule in supervised and unsupervised learning. The development of artificial learning towards these new goals and concepts might be achieved in the foreseeable future by perturbation around the current static teacher assumptions. It is also intriguing to investigate whether other types of artificial adaptive teachers, beside the biological prescription, also enhance learning.
The generalizations of the presented results to recurrent networks^{40,41,42} is intriguing and especially the estimation of the scaling of quantities such as number of attractors, their basin of attractions and capacity. In addition, it is intriguing to generalize the proposed biological model to Hamiltonian spin systems^{43} or to binary neuronal models, similar to the existing ones in computer science and statistical mechanics. This might lead to analytical solutions using the existing methods developed for such systems, as well as simplified simulations, which will shed light on learning in the general class of such artificial systems.
Methods
The feedforward network
The network consists of an input layer with N input units and an output unit functioning as a leaky integrated and fire (LIF) neuron (see Output production). The input units are connected to the output unit via N synaptic weights, \({w}_{m}\) (Fig. 2), or via K = N/5 dendritic strengths, \({J}_{i}\) (Fig. 3). In the synaptic scenario, \(\{{w}_{m}\}\) are the tunable parameters (Fig. 2), whereas for the dendritic scenario, \(\{{J}_{i}\}\) are the tunable parameters while \(\{{w}_{m}\}\) are timeindependent (Fig. 3).
The supervised learning algorithm
The scenario of supervised learning by a biological perceptron is examined using a teacher and a student. The mission of the student is to imitate the responses, i.e. the outputs, of the teacher, where both have the same architecture. For each input the teacher produces an output. The timings and the amplitudes as well as the resulting teacher’s outputs for each input unit, are provided to the student. Those input/output relations constitute the entire information provided to the student for each input. The algorithm is composed of 3 parts: output production, weights adaptation and learning.
Output production: An identical asynchronous input, example, is given to the teacher and the student, each produces its output according to their weights and decaying input summation, O^{T} and O^{S}, respectively (see Output production – Leaky integrate and fire neuron).
Weight adaptation: For each input unit the teacher preforms weights adaptation next to its output production, following its input/output (see Adaptation). The student preforms the same adaptation as the teacher, unless otherwise stated (see Student’s adaptation).
Learning: The student preforms learning steps, unless otherwise stated, on weights with conflicting outputs with the teacher, i.e. O_{m}^{T} ≠ O_{m}^{S} for the m^{th} input unit.
Inputs generation
Each input is composed of N/2 randomly stimulated input units. For each stimulated unit a random delay and a stimulation amplitude are chosen from given distributions. The delays are randomly chosen from a uniform distribution with a resolution of 0.01 ms, such that the average timelag between two consecutive stimulations is 5 ms. Stimulation amplitudes were randomly chosen from a uniform distribution in the range [0.8,1.2]. Note that the reported results are qualitatively robust to the scenario where all nonzero amplitudes equal 1. In the dendritic scenario, the five \({w}_{m}\) connected to the same dendrite were stimulated sequentially in a random order and with an average timelag of 5 ms between consecutive stimulations.
Output production – Leaky integrate and fire neuron
In the synaptic adaptation scenario, the voltage of the output unit is described by the leaky integrate and fire (LIF) model
where V(t) is the scaled voltage, Τ = 20 ms is the membrane time constant and V_{st} = 0 stands for the scaled stable (resting) membrane potential. \({w}_{m}\) and τ_{m} stand for the m^{th} weight and delay, respectively. A spike occurs when the voltage crosses the threshold, V(t) ≥ 1 and at that time the output unit produces an output of 1, otherwise the output is 0. After a spike occurs, the voltage is set to V_{st}. For simplicity, we scale the equation such that V_{th} = 1, V_{st} = 0, consequently, V ≥ 1 is above threshold and V < 1 is below threshold. Nevertheless, results remain the same for both the scaled and unscaled equations, e.g. V_{st} = −70 mV and V_{th} = −54 mV. The initial voltage was set to V_{(t = 0)} = 0.
In the dendritic adaptation scenario, the voltage of each dendritic terminal is described by
where V_{i}(t) and \({J}_{i}\) stand for the voltage and the strength of the i^{th} dendrite, respectively. The rest of the parameters are identical to the synaptic adaptation scenario.
Adaptation
The adaptation for the synaptic scenario, is done according to
where t is the timelag between a subthreshold stimulation to \({w}_{m}\) (stimulation that didn’t evoke spike, output 0) and an evoked spike. Similarly, the dendritic adaptation is given by
where t now is the timelag between a subthreshold stimulation at \({J}_{i}\) and an evoked spike from another dendrite. For both scenarios
representing the strengthening/weakening of a weight conditioned to a prior/later evoked spike at a time delay t, respectively, where a cutoff time window of 50 ms is enforced (Fig. S1). For simplicity, a step function,
was used for all time delay t, unless otherwise stated. However, all results are robust to adaptation in the form of either exponential decay or a step function.
Student’s adaptation
In order to perform the same adaptation as the teacher, the required information is the teacher’s temporal input/output relations. Note that although the student performs the same adaptation steps as the teacher, it does not necessarily ensure tracking of the parameters of the teacher, since the changes in the weights are relative to the current value of the weights of the student.
Learning
Learning steps were performed on the student’s weights with conflicting output with the teacher. This learning rule is based on a gradient descent dynamics, which minimizes a cost function
that measures the deviation of the student voltage form the teacher voltage in case of an error (unmatched spike timings between the teacher and the student). A spike is considered as V=1. The change in the weights \({w}_{m}\) is proportional to the negative derivative of the cost function relative to the weight.
For simplicity, the weighted exponential prefactor is neglected, but qualitative results remain similar for both cases. Consequently, the learning step for the synaptic scenario is similar to the traditional perceptron learning algorithm
and similarly for the dendritic scenario
λ denotes the learning step and O_{m}^{T} and O_{m}^{S} are the outputs of the teacher and the student at the m^{th} input unit in the i^{th} dendrite, respectively, and \({x}_{m}\) denotes the stimulation amplitude of the m^{th} input unit.
Calculating the generalization error
The generalization error is estimated every 2000 (1000) inputs in the synaptic (dendritic) scenario. The estimation consists of up to 250,000 inputs presented to the teacher and the student. The generalization error is defined as
For each measured ε_{g}(p) the generalization error is measured at least three times, and the average is presented with the largest error bar among all measured ε_{g}(p).
Figure 2: \(\{{w}_{m}\}\) were chosen from a uniform distribution in the range [0.1, 0.9] and then were normalized to a mean equals to 0.5. Adaptation was following Eq. (8) with A = 0.003, and learning was following Eq. (9) with λ = 1/1000. \({w}_{m}\) was bounded from above by 1.5 and from below by 10^{−4}.
In panel B, the STD of the generalization error was in the order of the size of the circles, and therefore not shown in the graph.
In panel C, two types of firing fractions are presented. The first consists of the total number of spikes normalized by N. The second indicates the number of spikes induced by input summation normalized by N, i.e. evoked spikes by weights obeying \({w}_{m}\cdot {x}_{m} < 1\).
In panel D, the normalized histogram of the synaptic weights at p = 6 * 10^{4} is plotted using 75 bins.
In panel E, the error of a perceptron was calculated according to
where R is the normalized overlap between the teacher’s and the student’s weights
Figure 3: \(\{{w}_{m}\}\) were chosen from a uniform distribution in the range [0.1, 0.9] and then were normalized to a mean equals to 0.5. \(\{{J}_{i}\}\) were chosen from a uniform distribution in the range [0.5, 1.5].
In panel B, stimulations with low amplitudes (0.01) were given to the N/2 unstimulated input units, resulting in nonfrozen \({J}_{i}\). In addition, adaptation was performed according to the spike timings of the two prior and two later stimulated dendrites, instead of using a cutoff in time. This modification was introduced to overcome the order of the delays in our setup, i.e. delays of w belonging to dendrite i are greater than delays of w belonging to dendrite i − 1. Consequently, using a cutoff might break the symmetry in the adaptation steps of J (number and strength) before and after the dendrite generating a spike. The adaptation follows Eq. (8) with A = 0.003 and the learning follow Eq. (9) with λ = 1/N. \({J}_{i}\) was bounded from below by 0.1 and from above by 2. The first p where \({J}^{T}\) and \({J}^{S}\) were identical is denoted on the xaxis, ε_{g} = 0.
In panel C, the normalized histogram of 75 bins is presented for the dynamics excluding the transient of the first 10,000 inputs. Similarly, the transient was excluded in the normalized histogram presented in the inset.
In panels D, E adaptation follows Eq. (7) with A = 0.05, and learning follows Eq. (9) with λ = 1/N. \({J}_{i}\) was bounded from below by 0.1 and from above by 2.5. The first p where the nonfrozen \({J}^{T}\) and \({J}^{S}\) were identical is denoted on the xaxis, ε_{g} = 0.
In panel F, the error of a perceptron was calculated similarly to the synaptic case, Eqs (12) and (13), with \({J}^{T}\) and \({J}^{S}\) instead of \({w}^{T}\) and \({w}^{S}\), respectively.
Figure 4: The network was composed of an input layer which was fully connected to a hidden layer, each consisted of N units, and a single output unit. All hidden units and the output unit functioned as LIF neurons (see Output production). The fixed delays in the first and the second layer were chosen randomly from a uniform distribution in the range [0, 5N/2] with a resolution of 0.001 ms, where the teacher and the student had the same architecture. Initial weights for both layers were chosen from a uniform distribution in the range [0.1,0.9] and were bounded from above by 1.5 and from below by 10^{−4}. An asynchronous input was given to N/2 randomly chosen input units. For each stimulated unit a random delay was chosen from a uniform distribution with a resolution of 0.001 ms, such that the average timelag between two consecutive stimulations was 5 ms. Stimulation amplitudes were set to 1. The delays were chosen such that stimulation routes from an input unit to the output unit were nondegenerated, i.e. no more than one stimulation arrived simultaneously to a unit. In the first step of the dynamics the hidden layer produced its outputs. Second, those outputs were used as the input to the output unit, which then produced its output. Finally, weights adaptation was performed using Eq. (7) with A = 0.001 and learning following Eq. (9) with λ = 0.002. For the first layer of weights the teacher and the student preformed weights adaptation according to their inputs and outputs of the hidden units. For the second layer of weights, the student performed adaptation according to the teacher’s spike timings and its own subthreshold stimulation timings. Learning steps were performed on the student’s weights of the first and the second layers with conflicting output with the teacher. Learning was based on the distinct stimulation routes, i.e. for each spike in the teacher’s output, the student knew which hidden unit evoked the spike. The error was calculated every 2000 inputs following Eq. (11), using the upper bound of the total number of stimulations, N^{2}/2. For N = 100 all the delays were chosen with a resolution of 0.0001 ms.
Figure S2: Parameters are the same as in Fig. 2, with A = 0.001 (Eq. 8) and λ = 50/N (Eq. 9).
Figure S6: Parameters are the same as in Fig. 3E, with λ = 1/1000 (Eq. 10).
Figure S7: Data extracted from Fig. 3E. The normalized overlap of \({J}_{i}\) was divided to the overlap of frozen and nonfrozen dendrites. A frozen dendrite was defined such that the variance of its strengths during the last 500 inputs was less than 10^{−3}. For each group the normalized overlap was calculated following Eq. (13) with \({J}^{T}\) and \({J}^{S}\) instead of \({w}^{T}\) and \({w}^{S}\), respectively.
Figure S8: For the synaptic scenario, data was extracted from simulation using the same parameters as in Fig. 2. After each input the following term was calculated for each stimulated weight
measuring whether the learning step decreases the gap between w^{T}(p − 1) and w^{S}(p − 1). In case the term, Eq. (14), was positive (negative) the step was classified as attractive (repulsive). For the dendritic scenario, data was extracted from simulation using the same parameters as in Fig. 3B, and the attractive/repulsive steps were calculated using Eq. (14) with \({J}^{T}\) and \({J}^{S}\) instead of \({w}^{T}\) and \({w}^{S}\), respectively.
Data Availability
All data generated or analyzed during this study are included in this published article (and its Supplementary Information (SI) Files).
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H.U. and S.S. contributed equally to this work. H.U. and S.S. developed the theoretical concepts, ran the simulations and analyzed the data under the guidance of I.K. All authors discussed the results and commented on the manuscript. I.K. initiated the study and supervised all aspects of the work.
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Uzan, H., Sardi, S., Goldental, A. et al. Biological learning curves outperform existing ones in artificial intelligence algorithms. Sci Rep 9, 11558 (2019). https://doi.org/10.1038/s41598019480164
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DOI: https://doi.org/10.1038/s41598019480164
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