Searcharxiv⌕ Search

arXiv subjects

Guillaume Drion

Publications and source records attributed to Guillaume Drion.

31 records · Page 2Linked to original sources

A bio-inspired bistable recurrent cell allows for long-lasting memory

Recurrent neural networks (RNNs) provide state-of-the-art performances in a wide variety of tasks that require memory. These performances can often be achieved thanks to gated recurrent cells such as gated recurrent units (GRU) and long short-term memory (LSTM). Standard gated cells share a layer internal state to store information at the network level, and long term memory is shaped by network-wide recurrent connection weights. Biological neurons on the other hand are capable of holding information at the cellular level for an arbitrary long amount of time through a process called bistability. Through bistability, cells can stabilize to different stable states depending on their own past state and inputs, which permits the durable storing of past information in neuron state. In this work, we take inspiration from biological neuron bistability to embed RNNs with long-lasting memory at the cellular level. This leads to the introduction of a new bistable biologically-inspired recurrent cell that is shown to strongly improves RNN performance on time-series which require very long memory, despite using only cellular connections (all recurrent connections are from neurons to themselves, i.e. a neuron state is not influenced by the state of other neurons). Furthermore, equipping this cell with recurrent neuromodulation permits to link them to standard GRU cells, taking a step towards the biological plausibility of GRU.

cs.NE↗

Introducing Neuromodulation in Deep Neural Networks to Learn Adaptive Behaviours

Animals excel at adapting their intentions, attention, and actions to the environment, making them remarkably efficient at interacting with a rich, unpredictable and ever-changing external world, a property that intelligent machines currently lack. Such an adaptation property relies heavily on cellular neuromodulation, the biological mechanism that dynamically controls intrinsic properties of neurons and their response to external stimuli in a context-dependent manner. In this paper, we take inspiration from cellular neuromodulation to construct a new deep neural network architecture that is specifically designed to learn adaptive behaviours. The network adaptation capabilities are tested on navigation benchmarks in a meta-reinforcement learning context and compared with state-of-the-art approaches. Results show that neuromodulation is capable of adapting an agent to different tasks and that neuromodulation-based approaches provide a promising way of improving adaptation of artificial systems.

cs.LG↗

Cellular switches orchestrate rhythmic circuits

Small inhibitory neuronal circuits have long been identified as key neuronal motifs to generate and modulate the coexisting rhythms of various motor functions. Our paper highlights the role of a cellular switching mechanism to orchestrate such circuits. The cellular switch makes the circuits reconfigurable, robust, adaptable, and externally controllable. Without this cellular mechanism, the circuits rhythms entirely rely on specific tunings of the synaptic connectivity, which makes them rigid, fragile, and difficult to control externally. We illustrate those properties on the much studied architecture of a small network controlling both the pyloric and gastric rhythms of crabs. The cellular switch is provided by a slow negative conductance often neglected in mathematical modeling of central pattern generators. We propose that this conductance is simple to model and key to computational studies of rhythmic circuit neuromodulation.

q-bio.NC↗

Robust and tunable bursting requires slow positive feedback

We highlight that the robustness and tunability of a bursting model critically relies on currents that provide slow positive feedback to the membrane potential. Such currents have the ability of making the total conductance of the circuit negative in a time scale that is termed slow because intermediate between the fast time scale of the spike upstroke and the ultraslow time scale of even slower adaptation currents. We discuss how such currents can be assessed either in voltage-clamp experiments or in computational models. We show that, while frequent in the literature, mathematical and computational models of bursting that lack the slow negative conductance are fragile and rigid. Our results suggest that modeling the slow negative conductance of cellular models is important when studying the neuromodulation of rhythmic circuits at any broader scale.

q-bio.NC↗

Robust modulation of integrate-and-fire models

By controlling the state of neuronal populations, neuromodulators ultimately affect behaviour. A key neuromodulation mechanism is the alteration of neuronal excitability via the modulation of ion channel expression. This type of neuromodulation is normally studied via conductance-based models, but those models are computationally challenging for large-scale network simulations needed in population studies. This paper studies the modulation properties of the Multi-Quadratic Integrate-and-Fire (MQIF) model, a generalisation of the classical Quadratic Integrate-and-Fire (QIF) model. The model is shown to combine the computational economy of integrate-and-fire modelling and the physiological interpretability of conductance-based modelling. It is therefore a good candidate for affordable computational studies of neuromodulation in large networks.

q-bio.NC↗

Excitable behaviors

This chapter revisits the concept of excitability, a basic system property of neurons. The focus is on excitable systems regarded as behaviors rather than dynamical systems. By this we mean open systems modulated by specific interconnection properties rather than closed systems classified by their parameter ranges. Modeling, analysis, and synthesis questions can be formulated in the classical language of circuit theory. The input-output characterization of excitability is in terms of the local sensitivity of the current-voltage relationship. It suggests the formulation of novel questions for non-linear system theory, inspired by questions from experimental neurophysiology.

q-bio.NC↗

A positive feedback at the cellular level promotes robustness and modulation at the circuit level

The paper highlights the role of a positive feedback gating mechanism at the cellular level in the robust- ness and modulation properties of rhythmic activities at the circuit level. The results are presented in the context of half-center oscillators, which are simple rhythmic circuits composed of two reciprocally connected inhibitory neuronal populations. Specifically, we focus on rhythms that rely on a particu- lar excitability property, the post-inhibitory rebound, an intrinsic cellular property that elicits transient membrane depolarization when released from hyperpolarization. Two distinct ionic currents can evoke this transient depolarization: a hyperpolarization-activated cation current and a low-threshold T-type calcium current. The presence of a slow activation is specific to the T-type calcium current and provides a slow-positive feedback at the cellular level that is absent in the cation current. We show that this slow- positive feedback is necessary and sufficient to endow the network rhythm with physiological modulation and robustness properties. This study thereby identifies an essential cellular property to be retained at the network level in modeling network robustness and modulation.

q-bio.NC↗

Modeling the modulation of neuronal bursting: a singularity theory approach

Exploiting the specific structure of neuron conductance-based models, the paper investigates the mathematical modeling of neuronal bursting modulation. The proposed approach combines singularity theory and geometric singular perturbations to capture the geometry of multiple time-scales attractors in the neighborhood of high-codimension singularities. We detect a three-time scale bursting attractor in the universal unfolding of the winged cusp singularity and discuss the physiological relevance of the bifurcation and unfolding parameters in determining a physiological modulation of bursting. The results suggest generality and simplicity in the organizing role of the winged cusp singularity for the global dynamics of conductance based models.

math.DS↗

Modulation of beta oscillations during movement initiation: modeling the ionic basis of a functional switch

We use a computational model to propose a physiological mechanism by which transient control of beta oscillations in the indirect pathway of the basal ganglia is orchestrated at the cellular level. Our model includes a simple and robust mechanism by which a cellular switch (from bursting to tonic) almost instantaneously translates into a functional gating switch (from blocking to conducive) in an excitatory-inhibitory network. Applied to the control of beta oscillations in the basal ganglia, the model shows the modulation of beta activity under the action of a transient depolarization, for instance a dopamine signal. The model predicts, by analogy to the thalamocortical circuit, a novel gating function by which the transfer of cortical spikes through the indirect pathway is blocked under the inhibitory drive preceding movement but briefly released at the onset of movement execution.

q-bio.NC↗

Modulation and Robustness of Endogenous Neuronal Spiking

Neuronal spiking exhibits an exquisite combination of modulation and robustness properties, rarely matched in artificial systems. We exploit the particular interconnection structure of conductance based models to investigate this remarkable property. We find that much of neuronal modulation and robustness can be explained by separating the total transmembrane current into three different components corresponding to the three time scales of neuronal bursting. Each equivalent current aggregates many ionic contributions into an equivalent voltage-dependent conductance, which defines a key modulation parameter. Plugging those equivalent feedback gains in a minimal abstract model recovers many experimental modulation scenarii as modulatory paths in elementary two-parameter charts. Likewise, robustness owes to the many possible physiological realizations of a same equivalent conductance, highlighting the role of equivalent conductances as prominent targets for neuromodulation and intrinsic homeostasis.

q-bio.NC↗

A Balance Equation Determines a Switch in Neuronal Excitability

We use the qualitative insight of a planar neuronal phase portrait to detect an excitability switch in arbitrary conductance-based models from a simple mathematical condition. The condition expresses a balance between ion channels that provide a negative feedback at resting potential (restorative channels) and those that provide a positive feedback at resting potential (regenerative channels). Geometrically, the condition imposes a transcritical bifurcation that rules the switch of excitability through the variation of a single physiological parameter. Our analysis of six different published conductance based models always finds the transcritical bifurcation and the associated switch in excitability, which suggests that the mathematical predictions have a physiological relevance and that a same regulatory mechanism is potentially involved in the excitability and signaling of many neurons.

q-bio.NC↗

An organizing center in a planar model of neuronal excitability

The paper studies the excitability properties of a generalized FitzHugh-Nagumo model. The model differs from the purely competitive FitzHugh-Nagumo model in that it accounts for the effect of cooperative gating variables such as activation of calcium currents. Excitability is explored by unfolding a pitchfork bifurcation that is shown to organize five different types of excitability. In addition to the three classical types of neuronal excitability, two novel types are described and distinctly associated to the presence of cooperative variables.

math.DS↗

A Novel Phase Portrait to Understand Neuronal Excitability

Fifty years ago, Fitzugh introduced a phase portrait that became famous for a twofold reason: it captured in a physiological way the qualitative behavior of Hodgkin-Huxley model and it revealed the power of simple dynamical models to unfold complex firing patterns. To date, in spite of the enormous progresses in qualitative and quantitative neural modeling, this phase portrait has remained the core picture of neuronal excitability. Yet, a major difference between the neurophysiology of 1961 and of 2011 is the recognition of the prominent role of calcium channels in firing mechanisms. We show that including this extra current in Hodgkin-Huxley dynamics leads to a revision of Fitzugh-Nagumo phase portrait that affects in a fundamental way the reduced modeling of neural excitability. The revisited model considerably enlarges the modeling power of the original one. In particular, it captures essential electrophysiological signatures that otherwise require non-physiological alteration or considerable complexication of the classical model. As a basic illustration, the new model is shown to highlight a core dynamical mechanism by which the calcium conductance controls the two distinct firing modes of thalamocortical neurons.

math.DS↗