Dynamics of phase locking in neuronal networks in the presence of synaptic plasticity

The behavior generated by neuronal networks depends on the phase relationships of its individual neurons. Observed phases result from the combined effects of individual cells and synaptic connections whose properties change dynamically. The properties of individual cells and synapses can often be characterized by driving the cell or synapse with inputs that arrive at different phases or frequencies, thus producing a feed-forward description of these properties. In this study, a recurrent network of two oscillatory neurons that are coupled with reciprocal synapses is considered. Feed-forward descriptions of the phase response curves of the neurons and the short-term synaptic plasticity properties are used to define Poincar´e maps for the activity of the network. The fixed points of these maps correspond to the phase locked modes of the network. These maps allow analysis of the dependence of the resulting network activity on the properties of network components. Using a combination of analysis and simulations, how various parameters of the model affect the existence and stability of phase-locked solutions is shown. It is also shown that synaptic plasticity provides flexibility and supports phase maintenance in networks. Conditions are found on the synaptic plasticity profiles and the phase response curves of the neurons for the network to be able to maintain a constant firing period, while varying the relative activity phase of the neurons or vice versa. Synaptic plasticity is shown to yield bistable phase locking modes. These results are geometrically demonstrated using a generalization to cobwebbing for two dimensional maps. Type I neurons modeled with Morris-Lecar and Quadratic Integrate-and-Fire are used to estimate the predictive power of the analytical results; however, the results hold in general. The properties of the Negative-Leak model are also studied; a recent conductance-based model which is obtained by replacing a regenerative inward current with a negative-slope-conductance linear current. The map methods are extended to analyze networking properties of Negative-Leak neurons by including burst response curves. Finally, geometric singular perturbation techniques are applied to analyze how a hyperpolarization-activated inward current contributes to the generation of oscillations in this model. This work introduces a general method to determine how changes in the phase response curves or synaptic dynamics affect phase locking in a recurrent network which can be generalized to study larger networks

Using feed-forward networks to infer the activity of feedback neuronal networks

The nervous system is one of the most important organ systems in a multicellular body. Animals, including human beings perceive, learn, think and deliver motion instructions through their nervous system. The basic structural units of the nervous system are individual neurons which constitute different neuronal networks with distinct functions. In each network, constituent neurons are coupled with different connection patterns, for example, some neurons send feed-forward information to the coupling neurons while others are mutually coupled. Because it is often difficult to analyze large interconnected feedback neuronal networks, it is important to derive techniques to reduce the complexity of the analysis. My research focuses on using the information of different feed-forward neuronal networks to infer the activity of feedback networks. To accomplish this objective, I use geometric analysis combined with numerical simulations for some typical neuronal systems to determine the activity of the feedback neuronal network in the context of central pattern generating networks. In my study, I am interested in deriving reduced methods to understand the combined effect of short-term plasticity on the phase-locked activity of networks. I consider a network of two reciprocally coupled heterogenous neurons, A and B, with synaptic depression from neuron A to neuron B. Suppose we are given two pieces of feed-forward information, the effect of neuron A on the activity of neuron B in the feed-forward network of A entraining B and vice versa. Moreover, suppose these effects are not limited to the weak coupling regime. We have developed a method to combine these pieces of feed-forward information into a 2D map that predicts the activity phase of these two neurons when they are mutually coupled. The analysis of the map is based on certain geometric constructs that arise from each of the feed-forward processes. Our analysis has two parts corresponding to different intrinsic firing patterns of these two neurons. In the first part, we assume that neuron A is oscillatory, while neuron B is not. In the second part, both neurons A and B are assumed to be oscillatory. Both sets of assumptions lead to different feedback maps

Loss of synchrony in an inhibitory network of type-I oscillators

Synchronization of excitable cells coupled by reciprocal inhibition is a topic of significant interest due to the important role that inhibitory synaptic interaction plays in the generation and regulation of coherent rhythmic activity in a variety of neural systems. While recent work revealed the synchronizing influence of inhibitory coupling on the dynamics of many networks, it is known that strong coupling can destabilize phase-locked firing. Here we examine the loss of synchrony caused by an increase in inhibitory coupling in networks of type-I Morris-Lecar model oscillators, which is characterized by a period-doubling cascade and leads to mode-locked states with alternation in the firing order of the two cells, as reported recently by Maran and Canavier (2007) for a network of Wang-Buzsáki model neurons. Although alternating- order firing has been previously reported as a near-synchronous state, we show that the stable phase difference between the spikes of the two Morris-Lecar cells can constitute as much as 70% of the unperturbed oscillation period. Further, we examine the generality of this phenomenon for a class of type-I oscillators that are close to their excitation thresholds, and provide an intuitive geometric description of such leap-frog dynamics. In the Morris-Lecar model network, the alternation in the firing order arises under the condition of fast closing of K+ channels at hyperpolarized potentials, which leads to slow dynamics of membrane potential upon synaptic inhibition, allowing the presynaptic cell to advance past the postsynaptic cell in each cycle of the oscillation. Further, we show that non-zero synaptic decay time is crucial for the existence of leap-frog firing in networks of phase oscillators. However, we demonstrate that leap-frog spiking can also be obtained in pulse-coupled inhibitory networks of one-dimensional oscillators with a multi-branched phase domain, for instance in a network of quadratic integrate-and-fire model cells. Also, we show that the entire bifurcation structure of the network can be explained by a simple scaling of the STRC (spike- time response curve) amplitude, using a simplified quadratic STRC as an example, and derive the general conditions on the shape of the STRC function that leads to leap-frog firing. Further, for the case of a homogeneous network, we establish quantitative conditions on the phase resetting properties of each cell necessary for stable alternating-order spiking, complementing the analysis of Goel and Ermentrout (2002) of the order-preserving phase transition map. We show that the extension of STRC to negative values of phase is necessary to predict the response of a model cell to several close non-weak perturbations. This allows us for instance to accurately describe the dynamics of non-weakly coupled network of three model cells. Finally, the phase return map is also extended to the heterogenous network, and is used to analyze both the order-alternating firing and the order-preserving non-zero phase locked state in this case

Synchronization in Neuronal Networks with Electrical and Chemical Coupling

Synchronized cortical activities in the central nervous systems of mammals are crucial for sensory perception, coordination, and locomotory function. The neuronal mechanisms that generate synchronous synaptic inputs in the neocortex are far from being fully understood. This thesis contributes toward an understanding of the emergence of synchronization in networks of bursting neurons as a highly nontrivial, combined effect of chemical and electrical connections. The first part of this thesis addresses the onset of synchronization in networks of bursting neurons coupled via both excitatory and inhibitory connections. We show that the addition of pairwise repulsive inhibition to excitatory networks of bursting neurons induces synchrony, in contrast to one’s expectations. Through stability analysis, we reveal the mechanism underlying this purely synergistic phenomenon and demonstrates that it originates from the transition between different types of bursting, caused by excitatory-inhibitory synaptic coupling. We also report a universal scaling law for the synchronization stability condition for large networks in terms of the number of excitatory and inhibitory inputs each neuron receives, regardless of the network size and topology. In the second part of this thesis, we show that similar effects are also observed in other models of bursting neurons, capable of switching from square-wave to plateau bursting. Finally, in the third part, we report a counterintuitive find that combined electrical and inhibitory coupling can synergistically induce robust synchronization in a range of parameters where electrical coupling alone promotes anti-phase spiking and inhibition induces anti-phase bursting. We reveal the underlying mechanism which uses a balance between hidden properties of electrical and inhibitory coupling to act together to synchronize neuronal bursting. We show that this balance is controlled by the duty cycle of the self-coupled system which governs the synchronized bursting rhythm. This work has potential implications for understanding the emergence of abnormal synchrony in epileptic brain networks. It suggests that promoting presumably desynchronizing inhibition in an attempt to prevent seizures can have a counterproductive effect and induce abnormal synchronous firing

Neutral coding - A report based on an NRP work session

Neural coding by impulses and trains on single and multiple channels, and representation of information in nonimpulse carrier

Understanding spiking and bursting electrical activity through piece-wise linear systems

In recent years there has been an increased interest in working with piece-wise linear caricatures of nonlinear models. Such models are often preferred over more detailed conductance based models for their small number of parameters and low computational overhead. Moreover, their piece-wise linear (PWL) form, allow the construction of action potential shapes in closed form as well as the calculation of phase response curves (PRC). With the inclusion of PWL adaptive currents they can also support bursting behaviour, though remain amenable to mathematical analysis at both the single neuron and network level. In fact, PWL models caricaturing conductance based models such as that of Morris-Lecar or McKean have also been studied for some time now and are known to be mathematically tractable at the network level. In this work we proceed to analyse PWL neuron models of conductance type. In particular we focus on PWL models of the FitzHugh-Nagumo type and describe in detail the mechanism for a canard explosion. This model is further explored at the network level in the presence of gap junction coupling. The study moves to a different area where excitable cells (pancreatic beta-cells) are used to explain insulin secretion phenomena. Here, Ca2+ signals obtained from pancreatic beta-cells of mice are extracted from image data and analysed using signal processing techniques. Both synchrony and functional connectivity analyses are performed. As regards to PWL bursting models we focus on a variant of the adaptive absolute IF model that can support bursting. We investigate the bursting electrical activity of such models with an emphasis on pancreatic beta-cells

Neuronal oscillations: from single-unit activity to emergent dynamics and back

L’objectiu principal d’aquesta tesi és avançar en la comprensió del processament d’informació en xarxes neuronals en presència d’oscil lacions subumbrals. La majoria de neurones propaguen la seva activitat elèctrica a través de sinapsis químiques que són activades, exclusivament, quan el corrent elèctric que les travessa supera un cert llindar. És per aquest motiu que les descàrregues ràpides i intenses produïdes al soma neuronal, els anomenats potencials d’acció, són considerades la unitat bàsica d’informació neuronal, és a dir, el senyal mínim i necessari per a iniciar la comunicació entre dues neurones. El codi neuronal és entès, doncs, com un llenguatge binari que expressa qualsevol missatge (estímul sensorial, memòries, etc.) en un tren de potencials d’acció. Tanmateix, cap funció cognitiva rau en la dinàmica d’una única neurona. Circuits de milers de neurones connectades entre sí donen lloc a determinats ritmes, palesos en registres d’activitat colectiva com els electroencefalogrames (EEG) o els potencials de camp local (LFP). Si els potencials d’acció de cada cèl lula, desencadenats per fluctuacions estocàstiques de les corrents sinàptiques, no assolissin un cert grau de sincronia, no apareixeria aquesta periodicitat a nivell de xarxa. Per tal de poder entendre si aquests ritmes intervenen en el codi neuronal hem estudiat tres situacions. Primer, en el Capítol 2, hem mostrat com una cadena oberta de neurones amb un potencial de membrana intrínsecament oscil latori filtra un senyal periòdic arribant per un dels extrems. La resposta de cada neurona (pulsar o no pulsar) depèn de la seva fase, de forma que cada una d’elles rep un missatge filtrat per la precedent. A més, cada potencial d’acció presinàptic provoca un canvi de fase en la neurona postsinàptica que depèn de la seva posició en l’espai de fases. Els períodes d’entrada capaços de sincronitzar les oscil lacions subumbrals són aquells que mantenen la fase d’arribada dels potencials d’acció fixa al llarg de la cadena. Per tal de què el missatge arribi intacte a la darrera neurona cal, a més a més, que aquesta fase permeti la descàrrega del voltatge transmembrana. En segon cas, hem estudiat una xarxa neuronal amb connexions tant a veïns propers com de llarg abast, on les oscil lacions subumbrals emergeixen de l’activitat col lectiva reflectida en els corrents sinàptics (o equivalentment en el LFP). Les neurones inhibidores aporten un ritme a l’excitabilitat de la xarxa, és a dir, que els episodis en què la inhibició és baixa, la probabilitat d’una descàrrega global de la població neuronal és alta. En el Capítol 3 mostrem com aquest ritme implica l’aparició d’una bretxa en la freqüència de descàrrega de les neurones: o bé polsen espaiadament en el temps o bé en ràfegues d’elevada intensitat. La fase del LFP determina l’estat de la xarxa neuronal codificant l’activitat de la població: els mínims indiquen la descàrrega simultània de moltes neurones que, ocasionalment, han superat el llindar d’excitabilitat degut a un decreixement global de la inhibició, mentre que els màxims indiquen la coexistència de ràfegues en diferents punts de la xarxa degut a decreixements locals de la inhibició en estats globals d’excitació. Aquesta dinàmica és possible gràcies al domini de la inhibició sobre l’excitació. En el Capítol 4 considerem acoblament entre dues xarxes neuronals per tal d’estudiar la interacció entre ritmes diferents. Les oscil lacions indiquen recurrència en la sincronització de l’activitat col lectiva, de manera que durant aquestes finestres temporals una població optimitza el seu impacte en una xarxa diana. Quan el ritme de la població receptora i el de l’emissora difereixen significativament, l’eficiència en la comunicació decreix, ja que les fases de màxima resposta de cada senyal LFP no mantenen una diferència constant entre elles. Finalment, en el Capítol 5 hem estudiat com les oscil lacions col lectives pròpies de l’estat de son donen lloc al fenomen de coherència estocàstica. Per a una intensitat òptima del soroll, modulat per l’excitabilitat de la xarxa, el LFP assoleix una regularitat màxima donant lloc a un període refractari de la població neuronal. En resum, aquesta Tesi mostra escenaris d’interacció entre els potencials d’acció, característics de la dinàmica de neurones individuals, i les oscil lacions subumbrals, fruit de l’acoblament entre les cèl lules i ubiqües en la dinàmica de poblacions neuronals. Els resultats obtinguts aporten funcionalitat a aquests ritmes emergents, agents sincronitzadors i moduladors de les descàrregues neuronals i reguladors de la comunicació entre xarxes neuronals.The main objective of this thesis is to better understand information processing in neuronal networks in the presence of subthreshold oscillations. Most neurons propagate their electrical activity via chemical synapses, which are only activated when the electric current that passes through them surpasses a certain threshold. Therefore, fast and intense discharges produced at the neuronal soma (the action potentials or spikes) are considered the basic unit of neuronal information. The neuronal code is understood, then, as a binary language that expresses any message (sensory stimulus, memories, etc.) in a train of action potentials. Circuits of thousands of interconnected neurons give rise to certain rhythms, revealed in collective activity measures such as electroencephalograms (EEG) and local field potentials (LFP). Synchronization of action potentials of each cell, triggered by stochastic fluctuations of the synaptic currents, cause this periodicity at the network level.To understand whether these rhythms are involved in the neuronal code we studied three situations. First, in Chapter 2, we showed how an open chain of neurons with an intrinsically oscillatory membrane potential filters a periodic signal coming from one of its ends. The response of each neuron (to spike or not) depends on its phase, so that each cell receives a message filtered by the preceding one. Each presynaptic action potential causes a phase change in the postsynaptic neuron, which depends on its position in the phase space. Those incoming periods that are able to synchronize the subthreshold oscillations, keep the phase of arrival of action potentials fixed along the chain. The original message reaches intact the last neuron provided that this phase allows the discharge of the transmembrane voltage.I the second case, we studied a neuronal network with connections to both long range and close neighbors, in which the subthreshold oscillations emerge from the collective activity apparent in the synaptic currents. The inhibitory neurons provide a rhythm to the excitability of the network. When inhibition is low, the likelihood of a global discharge of the neuronal population is high. In Chapter 3 we show how this rhythm causes a gap in the discharge frequency of neurons: either they pulse single spikes or they fire bursts of high intensity. The LFP phase determines the state of the neuronal network, coding the activity of the population: its minima indicate the simultaneous discharge of many neurons, while its maxima indicate the coexistence of bursts due to local decreases of inhibition at global states of excitation. In Chapter 4 we consider coupling between two neural networks in order to study the interaction between different rhythms. The oscillations indicate recurrence in the synchronization of collective activity, so that during these time windows a population optimizes its impact on a target network. When the rhythm of the emitter and receiver population differ significantly, the communication efficiency decreases as the phases of maximum response of each LFP signal do not maintain a constant difference between them.Finally, in Chapter 5 we studied how oscillations typical of the collective sleep state give rise to stochastic coherence. For an optimal noise intensity, modulated by the excitability of the network, the LFP reaches a maximal regularity leading to a refractory period of the neuronal population.In summary, this Thesis shows scenarios of interaction between action potentials, characteristics of the dynamics of individual neurons, and the subthreshold oscillations, outcome of the coupling between the cells and ubiquitous in the dynamics of neuronal populations . The results obtained provide functionality to these emerging rhythms, triggers of synchronization and modulator agents of the neuronal discharges and regulators of the communication between neuronal networks