Frequency control in synchronized networks of inhibitory neurons

We analyze the control of frequency for a synchronized inhibitory neuronal network. The analysis is done for a reduced membrane model with a biophysically-based synaptic influence. We argue that such a reduced model can quantitatively capture the frequency behavior of a larger class of neuronal models. We show that in different parameter regimes, the network frequency depends in different ways on the intrinsic and synaptic time constants. Only in one portion of the parameter space, called `phasic', is the network period proportional to the synaptic decay time. These results are discussed in connection with previous work of the authors, which showed that for mildly heterogeneous networks, the synchrony breaks down, but coherence is preserved much more for systems in the phasic regime than in the other regimes. These results imply that for mildly heterogeneous networks, the existence of a coherent rhythm implies a linear dependence of the network period on synaptic decay time, and a much weaker dependence on the drive to the cells. We give experimental evidence for this conclusion.Comment: 18 pages, 3 figures, Kluwer.sty. J. Comp. Neurosci. (in press). Originally submitted to the neuro-sys archive which was never publicly announced (was 9803001

Emergence of global synchronization in directed excitatory networks of type I neurons

The collective behaviour of neural networks depends on the cellular and synaptic properties of the neurons. The phase-response curve (PRC) is an experimentally obtainable measure of cellular properties that quantifies the shift in the next spike time of a neuron as a function of the phase at which stimulus is delivered to that neuron. The neuronal PRCs can be classified as having either purely positive values (type I) or distinct positive and negative regions (type II). Networks of type 1 PRCs tend not to synchronize via mutual excitatory synaptic connections. We study the synchronization properties of identical type I and type II neurons, assuming unidirectional synapses. Performing the linear stability analysis and the numerical simulation of the extended Kuramoto model, we show that feedforward loop motifs favour synchronization of type I excitatory and inhibitory neurons, while feedback loop motifs destroy their synchronization tendency. Moreover, large directed networks, either without feedback motifs or with many of them, have been constructed from the same undirected backbones, and a high synchronization level is observed for directed acyclic graphs with type I neurons. It has been shown that, the synchronizability of type I neurons depends on both the directionality of the network connectivity and the topology of its undirected backbone. The abundance of feedforward motifs enhances the synchronizability of the directed acyclic graphs

A Model of Stimulus-Specific Neural Assemblies in the Insect Antennal Lobe

It has been proposed that synchronized neural assemblies in the antennal lobe of insects encode the identity of olfactory stimuli. In response to an odor, some projection neurons exhibit synchronous firing, phase-locked to the oscillations of the field potential, whereas others do not. Experimental data indicate that neural synchronization and field oscillations are induced by fast GABAA-type inhibition, but it remains unclear how desynchronization occurs. We hypothesize that slow inhibition plays a key role in desynchronizing projection neurons. Because synaptic noise is believed to be the dominant factor that limits neuronal reliability, we consider a computational model of the antennal lobe in which a population of oscillatory neurons interact through unreliable GABAA and GABAB inhibitory synapses. From theoretical analysis and extensive computer simulations, we show that transmission failures at slow GABAB synapses make the neural response unpredictable. Depending on the balance between GABAA and GABAB inputs, particular neurons may either synchronize or desynchronize. These findings suggest a wiring scheme that triggers stimulus-specific synchronized assemblies. Inhibitory connections are set by Hebbian learning and selectively activated by stimulus patterns to form a spiking associative memory whose storage capacity is comparable to that of classical binary-coded models. We conclude that fast inhibition acts in concert with slow inhibition to reformat the glomerular input into odor-specific synchronized neural assemblies

Membrane Properties and the Balance between Excitation and Inhibition Control Gamma-Frequency Oscillations Arising from Feedback Inhibition

Computational studies as well as in vivo and in vitro results have shown that many cortical neurons fire in a highly irregular manner and at low average firing rates. These patterns seem to persist even when highly rhythmic signals are recorded by local field potential electrodes or other methods that quantify the summed behavior of a local population. Models of the 30–80 Hz gamma rhythm in which network oscillations arise through ‘stochastic synchrony’ capture the variability observed in the spike output of single cells while preserving network-level organization. We extend upon these results by constructing model networks constrained by experimental measurements and using them to probe the effect of biophysical parameters on network-level activity. We find in simulations that gamma-frequency oscillations are enabled by a high level of incoherent synaptic conductance input, similar to the barrage of noisy synaptic input that cortical neurons have been shown to receive in vivo. This incoherent synaptic input increases the emergent network frequency by shortening the time scale of the membrane in excitatory neurons and by reducing the temporal separation between excitation and inhibition due to decreased spike latency in inhibitory neurons. These mechanisms are demonstrated in simulations and in vitro current-clamp and dynamic-clamp experiments. Simulation results further indicate that the membrane potential noise amplitude has a large impact on network frequency and that the balance between excitatory and inhibitory currents controls network stability and sensitivity to external inputs

Gamma Oscillations in a Nonlinear Regime: A Minimal Model Approach Using Heterogeneous Integrate-and-Fire Networks

Fast oscillations and in particular gamma-band oscillation (20-80 Hz) are commonly observed during brain function and are at the center of several neural processing theories. In many cases, mathematical analysis of fast oscillations in neural networks has been focused on the transition between irregular and oscillatory firing viewed as an instability of the asynchronous activity. But in fact, brain slice experiments as well as detailed simulations of biological neural networks have produced a large corpus of results concerning the properties of fully developed oscillations that are far from this transition point. We propose here a mathematical approach to deal with nonlinear oscillations in a network of heterogeneous or noisy integrate-and-fire neurons connected by strong inhibition. This approach involves limited mathematical complexity and gives a good sense of the oscillation mechanism, making it an interesting tool to understand fast rhythmic activity in simulated or biological neural networks. A surprising result of our approach is that under some conditions, a change of the strength of inhibition only weakly influences the period of the oscillation. This is in contrast to standard theoretical and experimental models of interneuron network gamma oscillations (ING), where frequency tightly depends on inhibition strength, but it is similar to observations made in some in vitro preparations in the hippocampus and the olfactory bulb and in some detailed network models. This result is explained by the phenomenon of suppression that is known to occur in strongly coupled oscillating inhibitory networks but had not yet been related to the behavior of oscillation frequency

Toward optogenetic control of neural synchrony : experimental results from the hippocampal slice model of gamma oscillations and computational modeling

Thesis (S.M.)--Massachusetts Institute of Technology, School of Architecture and Planning, Program in Media Arts and Sciences, 2009.Cataloged from PDF version of thesis.Includes bibliographical references (p. 52-58).Ever since Hans Berger recorded the first human EEGs in humans and observed large, rhythmic 8 Hz field oscillations, neuroscientists have been intrigued by the pervasive presence of synchronized, regular patterns of the activity in the brain. A number of frequency bands, spanning from 0.1 to several hundred hertz have been described, and associated with particular functions and brain states. Not surprisingly, disruptions in such patterns have been postulated to be the mechanistic basis of a number of disorders, from schizophrenia to Parkinson's disease, to Alzheimer. Until now, however, virtually all evidence on the role of synchronous oscillations in brain functions has been merely correlative, that is, it has never been possible to selectively manipulate neural synchrony without altering other fundamental properties of the system and observing the functional outcome. This limit may now be overcome with the introduction of genetically targeted light-activeatable means of controlling neural activity, which allows spatially and temporally precise control of the activity of determined classes of neurons. Although the ultimate goal is to observe the functional, behavioral outcomes of modulating synchrony in awake animals, it's necessary first to develop such techniques in vitro, if we are to be able (given the current technological limitations) to extract useful "design principles" that can meaningfully generalize. A particularly well-studied, reliable and yet relevant in vitro model, is the hippocampal slice gamma oscillations model, so we have been focusing on those as a testbed, integrating experimental work with computational modeling. Among the previously undescribed capabilities we have gained in the process are: precisely resetting the phase of an ongoing gamma oscillation, altering its frequency, and modulating its amplitude.by Giovanni Talei Franzesi.S.M

Reconciliation of weak pairwise spike-train correlations and highly coherent local field potentials across space

Chronic and acute implants of multi-electrode arrays that cover several mm$^2$ of neural tissue provide simultaneous access to population signals like extracellular potentials and the spiking activity of 100 or more individual neurons. While the recorded data may uncover principles of brain function, its interpretation calls for multiscale computational models with corresponding spatial dimensions and signal predictions. Such models can facilitate the search of mechanisms underlying observed spatiotemporal activity patterns in cortex. Multi-layer spiking neuron network models of local cortical circuits covering ~1 mm$^2$ have been developed, integrating experimentally obtained neuron-type specific connectivity data and reproducing features of in-vivo spiking statistics. With forward models, local field potentials (LFPs) can be computed from the simulated spiking activity. To account for the spatial scale of common neural recordings, we extend a local network and LFP model to 4x4 mm$^2$. The upscaling preserves the neuron densities, and introduces distance-dependent connection probabilities and delays. As detailed experimental connectivity data is partially lacking, we address this uncertainty in model parameters by testing parameter combinations within biologically plausible bounds. Based on model predictions of spiking activity and LFPs, we find that the upscaling procedure preserves the overall spiking statistics of the original model and reproduces asynchronous irregular spiking across populations and weak pairwise spike-train correlations observed in sensory cortex. In contrast with the weak spike-train correlations, the correlation of LFP signals is strong and distance-dependent, compatible with experimental observations. Enhanced spatial coherence in the low-gamma band may explain the recent experimental report of an apparent band-pass filter effect in the spatial reach of the LFP.Comment: 44 pages, 9 figures, 5 table

Interacting Mechanisms Driving Synchrony in Neural Networks with Inhibitory Interneurons

Computational neuroscience contributes to our understanding of the brain by applying techniques from fields including mathematics, physics, and computer science to neuroscientific problems that are not amenable to purely biologic study. One area in which this interdisciplinary research is particularly valuable is the proposal and analysis of mechanisms underlying neural network behaviors. Neural synchrony, especially when driven by inhibitory interneurons, is a behavior of particular importance considering this behavior play a role in neural oscillations underlying important brain functions such as memory formation and attention. Typically, these oscillations arise from synchronous firing of a neural population, and thus the study of neural oscillations and neural synchrony are deeply intertwined. Such network behaviors are particularly amenable to computational analysis given the variety of mathematical techniques that are of use in this field. Inhibitory interneurons are thought to drive synchrony in ways described by two computational mechanisms: Interneuron Network Gamma (ING), which describes how an inhibitory network synchronizes itself; and Pyramidal Interneuron Network Gamma (PING), which describes how a population of interneurons inter-connected with a population of excitatory pyramidal cells (an E-I network) synchronizes both populations. As first articulated using simplified interneuron models, these mechanisms find network properties are the primary impetus for synchrony. However, as neurobiologists uncover interneurons exhibiting a vast array of cellular and intra-connectivity properties, our understanding of how interneurons drive oscillations must account for this diversity. This necessitates an investigation of how changing interneuron properties might disrupt the predictions of ING and PING, and whether other mechanisms might interact with or disrupt these network-driven mechanisms. In my dissertation, I broach this topic utilizing the Type I and Type II neuron classifications, which refer to properties derived from the mathematics of coupled oscillators. Classic ING and PING literature typically utilize Type I neurons which always respond to an excitatory perturbation with an advance of the subsequent action potential. However, many interneurons exhibit Type II properties, which respond to some excitatory perturbations with a delay in the subsequent action potential. Interneuronal diversity is also reflected in the strength and density of the synaptic connections between these neurons, which is also explored in this work. My research reveals a variety of ways in which interneuronal diversity alters synchronous oscillations in networks containing inhibitory interneurons and the mechanisms likely driving these dynamics. For example, oscillations in networks of Type II interneurons violate ING predictions and can be explained mechanistically primarily utilizing cellular properties. Additionally, varying the type of both excitatory and inhibitory cells in E-I networks reveals that synchronous excitatory activity arises with different network connectivities for different neuron types, sometimes driven by cellular properties rather than PING. Furthermore, E-I networks respond differently to varied strengths of inhibitory intra-connectivity depending upon interneuron type, sometimes in ways not fully accounted for by PING theory. Taken together, this research reveals that network-driven and cellularly-driven mechanisms promoting oscillatory activity in networks containing inhibitory interneurons interact, and oftentimes compete, in order to dictate the overall network dynamics. These dynamics are more complex than those predicted by the classic ING and PING mechanisms alone. The diverse dynamical properties imparted to oscillating neural networks by changing inhibitory interneuron properties provides some insight into the biological need for such variability.PHDApplied and Interdisciplinary MathematicsUniversity of Michigan, Horace H. Rackham School of Graduate Studieshttps://deepblue.lib.umich.edu/bitstream/2027.42/143981/1/sbrich_1.pd

The Use of Maps in the Analysis of Networks of Coupled Neuronal Oscillators

In this thesis we study aspects of periodic activity in model mutually-coupled oscillators inspired by the nervous system. We define and use maps describing the timing of activity on successive cycles. The central theme here is to examine emergent behavior in networks through the properties of the individual oscillators.In the first chapter, we describe Phase Response Curves (PRCs), which map the changes in theperiod of an oscillator to perturbations at dierent phases along the cycle. We consider various networks of oscillators, pulse-coupled through their PRCs: rings, chains, arrays, and global coupling.We study conditions under which stable patterns, such as synchrony and waves, may be found.In the second and third chapters, we model beta (12-30 Hz) and gamma (30-80 Hz) rhythmsin the nervous system in reduced networks of excitatory and inhibitory neurons. We look at theintriguing results of experiments that show increases in beta band activity in human MEGs upon taking the sedative Diapam. We show that the model network is able to mimic the experimental data. The model then clarifies the inhibitory action of the drug in tissue.We look at another experiment that finds disruption of long-range synchrony of gamma oscillations in transgenic mice with altered excitatory kinetics. We study this behavior in a reduced network that encodes for conduction delays across spatially distal sites. The model provides an explanation of this phenomenon in terms of the properties of the cells involved in generating the rhythm.In our analyses, we use maps to study stability of the patterns of activity

LOCAL AND TOP-DOWN REGULATION OF OLFACTORY BULB CIRCUITS

The olfactory bulb (OB) is the first place in the brain where chemosensory processing occurs. The neurophysiological mechanisms underlying these processes are mostly driven by inhibition, which is implemented by a large population of local inhibitory neurons, and among them, the granule cell (GCs) is the most prominent type. Local inhibitory interneurons sculpt the coding of output neurons, affecting odor detection, discrimination, and learning. Therefore, the regulation of inhibitory circuits is critical to OB function and fine-tuning OB output. Specifically, inhibitory tone in the OB can be regulated by the dynamic interactions between cell-intrinsic factors affecting neuronal excitability and extrinsic top-down modulation associated with an animal’s behavioral state. Here, I provide new evidence for intrinsic mechanisms governing inhibitory interneuron excitability in the OB and how modulation by noradrenaline works in concert with these intrinsic mechanisms to affect circuit function. This work highlights circuit- and cell-specific differences in noradrenergic modulation with regards to short- and long-term plasticity within OB circuits