35 research outputs found
Faculty Bibliography 2017
Bibliography of OWU faculty publications in 2016-2017
A biophysical model of dynamic balancing of excitation and inhibition in fast oscillatory large-scale networks
Over long timescales, neuronal dynamics can be robust to quite large perturbations, such as changes in white matter connectivity and grey matter structure through processes including learning, aging, development and certain disease processes. One possible explanation is that robust dynamics are facilitated by homeostatic mechanisms that can dynamically rebalance brain networks. In this study, we simulate a cortical brain network using the Wilson-Cowan neural mass model with conduction delays and noise, and use inhibitory synaptic plasticity (ISP) to dynamically achieve a spatially local balance between excitation and inhibition. Using MEG data from 55 subjects we find that ISP enables us to simultaneously achieve high correlation with multiple measures of functional connectivity, including amplitude envelope correlation and phase locking. Further, we find that ISP successfully achieves local E/I balance, and can consistently predict the functional connectivity computed from real MEG data, for a much wider range of model parameters than is possible with a model without ISP
Membrane resonance enables stable and robust gamma oscillations
Neuronal mechanisms underlying beta/gamma oscillations (20-80 Hz) are not completely understood. Here, we show that in vivo beta/gamma oscillations in the cat visual cortex sometimes exhibit remarkably stable frequency even when inputs fluctuate dramatically. Enhanced frequency stability is associated with stronger oscillations measured in individual units and larger power in the local field potential. Simulations of neuronal circuitry demonstrate that membrane properties of inhibitory interneurons strongly determine the characteristics of emergent oscillations. Exploration of networks containing either integrator or resonator inhibitory interneurons revealed that: (i) Resonance, as opposed to integration, promotes robust oscillations with large power and stable frequency via a mechanism called RING (Resonance INduced Gamma); resonance favors synchronization by reducing phase delays between interneurons and imposes bounds on oscillation cycle duration; (ii) Stability of frequency and robustness of the oscillation also depend on the relative timing of excitatory and inhibitory volleys within the oscillation cycle; (iii) RING can reproduce characteristics of both Pyramidal INterneuron Gamma (PING) and INterneuron Gamma (ING), transcending such classifications; (iv) In RING, robust gamma oscillations are promoted by slow but are impaired by fast inputs. Results suggest that interneuronal membrane resonance can be an important ingredient for generation of robust gamma oscillations having stable frequency
Analyses at microscopic, mesoscopic, and mean-field scales
Die Aktivität des Hippocampus im Tiefschlaf ist geprägt durch sharp wave-ripple Komplexe (SPW-R): kurze (50–100 ms) Phasen mit erhöhter neuronaler Aktivität, moduliert durch eine schnelle “Ripple”-Oszillation (140–220 Hz). SPW-R werden mit Gedächtniskonsolidierung in Verbindung gebracht, aber ihr Ursprung ist unklar. Sowohl exzitatorische als auch inhibitorische Neuronpopulationen könnten die Oszillation generieren.
Diese Arbeit analysiert Ripple-Oszillationen in inhibitorischen Netzwerkmodellen auf mikro-, meso- und makroskopischer Ebene und zeigt auf, wie die Ripple-Dynamik von exzitatorischem Input, inhibitorischer Kopplungsstärke und dem Rauschmodell abhängt.
Zuerst wird ein stark getriebenes Interneuron-Netzwerk mit starker, verzögerter Kopplung analysiert. Es wird eine Theorie entwickelt, die die Drift-bedingte Feuerdynamik im Mean-field Grenzfall beschreibt. Die Ripple-Frequenz und die Dynamik der Membranpotentiale werden analytisch als Funktion des Inputs und der Netzwerkparameter angenähert. Die Theorie erklärt, warum die Ripple-Frequenz im Verlauf eines SPW-R-Ereignisses sinkt (intra-ripple frequency accommodation, IFA). Weiterhin zeigt eine numerische Analyse, dass ein alternatives Modell, basierend auf einem transienten Störungseffekt in einer schwach gekoppelten Interneuron-Population, unter biologisch plausiblen Annahmen keine IFA erzeugen kann. IFA kann somit zur Modellauswahl beitragen und deutet auf starke, verzögerte inhibitorische Kopplung als plausiblen Mechanismus hin.
Schließlich wird die Anwendbarkeit eines kürzlich entwickelten mesoskopischen Ansatzes für die effiziente Simulation von Ripples in endlich großen Netzwerken geprüft. Dabei wird das Rauschen nicht im Input der Neurone beschrieben, sondern als stochastisches Feuern entsprechend einer Hazard-Rate. Es wird untersucht, wie die Wahl des Hazards die dynamische Suszeptibilität einzelner Neurone, und damit die Ripple-Dynamik in rekurrenten Interneuron-Netzwerken beeinflusst.Hippocampal activity during sleep or rest is characterized by sharp wave-ripples (SPW-Rs): transient (50–100 ms) periods of elevated neuronal activity modulated by a fast oscillation — the ripple (140–220 Hz). SPW-Rs have been linked to memory consolidation, but their generation mechanism remains unclear. Multiple potential mechanisms have been proposed, relying on excitation and/or inhibition as the main pacemaker.
This thesis analyzes ripple oscillations in inhibitory network models at micro-, meso-, and macroscopic scales and elucidates how the ripple dynamics depends on the excitatory drive, inhibitory coupling strength, and the noise model.
First, an interneuron network under strong drive and strong coupling with delay is analyzed. A theory is developed that captures the drift-mediated spiking dynamics in the mean-field limit. The ripple frequency as well as the underlying dynamics of the membrane potential distribution are approximated analytically as a function of the external drive and network parameters. The theory explains why the ripple frequency decreases over the course of an event (intra-ripple frequency accommodation, IFA). Furthermore, numerical analysis shows that an alternative inhibitory ripple model, based on a transient ringing effect in a weakly coupled interneuron population, cannot account for IFA under biologically realistic assumptions. IFA can thus guide model selection and provides new support for strong, delayed inhibitory coupling as a mechanism for ripple generation.
Finally, a recently proposed mesoscopic integration scheme is tested as a potential tool for the efficient numerical simulation of ripple dynamics in networks of finite size. This approach requires a switch of the noise model, from noisy input to stochastic output spiking mediated by a hazard function. It is demonstrated how the choice of a hazard function affects the linear response of single neurons and therefore the ripple dynamics in a recurrent interneuron network
Characterizing dynamically evolving functional networks in humans with application to speech
Understanding how communication between brain areas evolves to support dynamic function remains a fundamental challenge in neuroscience. One approach to this question is functional connectivity analysis, in which statistical coupling measures are employed to detect signatures of interactions between brain regions. Because the brain uses multiple communication mechanisms at different temporal and spatial scales, and because the neuronal signatures of communication are often weak, powerful connectivity inference methodologies require continued development specific to these challenges.
Here we address the challenge of inferring task-related functional connectivity in brain voltage recordings. We first develop a framework for detecting changes in statistical coupling that occur reliably in a task relative to a baseline period. The framework characterizes the dynamics of connectivity changes, allows inference on multiple spatial scales, and assesses statistical uncertainty. This general framework is modular and applicable to a wide range of tasks and research questions.
We demonstrate the flexibility of the framework in the second part of this thesis, in which we refine the coupling statistics and hypothesis tests to improve statistical power and test different proposed connectivity mechanisms. In particular, we introduce frequency domain coupling measures and define test statistics that exploit theoretical properties and capture known sampling variability. The resulting test statistics use correlation, coherence, canonical correlation, and canonical coherence to infer task-related changes in coupling. Because canonical correlation and canonical coherence are not commonly used in functional connectivity analyses, we derive the theoretical values and statistical estimators for these measures.
In the third part of this thesis, we present a sample application of these techniques to electrocorticography data collected during an overt reading task. We discuss the challenges that arise with task-related human data, which is often noisy and underpowered, and present functional connectivity results in the context of traditional and contemporary within-electrode analytics. In two of nine subjects we observe time-domain and frequency-domain network changes that accord with theoretical models of information routing during motor processing.
Taken together, this work contributes a methodological framework for inferring task-related functional connectivity across spatial and temporal scales, and supports insight into the rapid, dynamic functional coupling of human speech
25th annual computational neuroscience meeting: CNS-2016
The same neuron may play different functional roles in the neural circuits to which it belongs. For example, neurons in the Tritonia pedal ganglia may participate in variable phases of the swim motor rhythms [1]. While such neuronal functional variability is likely to play a major role the delivery of the functionality of neural systems, it is difficult to study it in most nervous systems. We work on the pyloric rhythm network of the crustacean stomatogastric ganglion (STG) [2]. Typically network models of the STG treat neurons of the same functional type as a single model neuron (e.g. PD neurons), assuming the same conductance parameters for these neurons and implying their synchronous firing [3, 4]. However, simultaneous recording of PD neurons shows differences between the timings of spikes of these neurons. This may indicate functional variability of these neurons. Here we modelled separately the two PD neurons of the STG in a multi-neuron model of the pyloric network. Our neuron models comply with known correlations between conductance parameters of ionic currents. Our results reproduce the experimental finding of increasing spike time distance between spikes originating from the two model PD neurons during their synchronised burst phase. The PD neuron with the larger calcium conductance generates its spikes before the other PD neuron. Larger potassium conductance values in the follower neuron imply longer delays between spikes, see Fig. 17.Neuromodulators change the conductance parameters of neurons and maintain the ratios of these parameters [5]. Our results show that such changes may shift the individual contribution of two PD neurons to the PD-phase of the pyloric rhythm altering their functionality within this rhythm. Our work paves the way towards an accessible experimental and computational framework for the analysis of the mechanisms and impact of functional variability of neurons within the neural circuits to which they belong
25th Annual Computational Neuroscience Meeting: CNS-2016
Abstracts of the 25th Annual Computational Neuroscience
Meeting: CNS-2016
Seogwipo City, Jeju-do, South Korea. 2–7 July 201
29th Annual Computational Neuroscience Meeting: CNS*2020
Meeting abstracts
This publication was funded by OCNS. The Supplement Editors declare that they have no competing interests.
Virtual | 18-22 July 202
Neuronal Network Oscillations in the Control of Human Movement
The overarching aim of this thesis was to use neuroimaging and neuromodulation techniques to further understand the relationship between cortical oscillatory activity and the control of human movement. Modulations in motor cortical beta and alpha
activity have been consistently implicated in the preparation, execution, and termination of movement. Here, I describe the outcome of four studies designed to further elucidate these motor-related changes in oscillatory activity.
In Chapter 3, I report the findings of a study that used an established behavioural paradigm to vary the degree of uncertainty during the preparation of movement. I demonstrate that preparatory alpha and beta desynchronisation reflect a process of
disengagement from the existing network to enable the creation of functional assemblies required for movement. Importantly, I also demonstrate a novel neural signature of transient alpha synchrony, that occurs after preparatory desynchronisation, that
underlies the recruitment of functional assemblies required for directional control.
The study described in Chapter 4 was designed to further investigate the functional role of preparatory alpha and beta desynchronisation by entraining oscillatory activity in the primary motor cortex (M1) using frequency-specific transcranial alternating current stimulation. No significant effects of stimulation were found on participant response times. However, no clear conclusion could be drawn due to limitations of the stimulation parameters that were used.
In Chapter 5, I explored the inverse relationship between M1 beta power and cortical excitability using single-pulse transcranial magnetic stimulation to elicit motor-evoked potentials (MEPs). The amplitude of MEPs collected during a period of beta
desynchronisation was significantly greater than during a resting baseline. Conversely, the amplitude of MEPs collected during the post-movement beta rebound that follows the termination of a movement was significantly reduced compared to baseline. This
finding confirms the inverse relationship between M1 beta power and cortical excitability.
The study in Chapter 6 explored the effect of experimental context on M1 beta power. When the participant was cued to expect an upcoming motor task, resting beta power was significantly increased, then when the likelihood of an upcoming motor requirement
decreased, there was a significant concurrent decrease in resting beta power. This reflects increased coherence and functional connectivity within M1 and other motor areas, to ‘recalibrate’ the motor system in preparation for a synchronous input signal to
more readily recruit the required functional assembly