Quantifying dynamics and variability in neural systems

Synchronized neural activity, in which the firing of neurons is coordinated in time, is an observed phenomenon in many neural functions. The conditions that promote synchrony and the dynamics of synchronized activity are active areas of investigation because they are incompletely understood. In addi...

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Main Author: Norman, Sharon Elizabeth
Other Authors: Butera, Robert J.
Format: Others
Language:en_US
Published: Georgia Institute of Technology 2016
Subjects:
Online Access:http://hdl.handle.net/1853/54269
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spelling ndltd-GATECH-oai-smartech.gatech.edu-1853-542692016-02-17T03:34:40ZQuantifying dynamics and variability in neural systemsNorman, Sharon ElizabethPhase resetting curveNeuronsVariabilityComputational neuroscienceElectrophysiologySynchronized neural activity, in which the firing of neurons is coordinated in time, is an observed phenomenon in many neural functions. The conditions that promote synchrony and the dynamics of synchronized activity are active areas of investigation because they are incompletely understood. In addition, variability is intrinsic to biological systems, but the effect of neuron spike time variability on synchronization dynamics is a question that merits more attention. Previous experiments using a hybrid circuit of one biological neuron coupled to one computational neuron revealed that irregularity in biological neuron spike timing could change synchronization in the circuit, transitioning the activity between phase-locked and phase slipping. Simulations of this circuit could not replicate the transitions in network activity if neuron period was represented as a Gaussian process, but could if a process with history and a stochastic component were used. The phase resetting curve (PRC), which describes how neuron cycles change in response to input, can be used to construct a map that predicts if synchronization will occur in hybrid circuits. Without modification, these maps did not always capture observed network activity. I conducted long-term recordings of invertebrate neurons and show that interspike interval (ISI) can be represented as an autoregressive integrated moving average process, where ISI is dependent on past history and a stochastic component with history. Using integrate and fire model simulations, I suggest that stochastic activity in adaptation channels could be responsible for the history dependence and correlational structure observed in these neurons. This evidence for stochastic, history-dependent noise in neural systems indicates that our understanding of network dynamics could be enhanced by including more complex, but relevant, forms of noise. I show that cycle-by-cycle dynamics of the coupled system can be used to infer features of the dynamic map, even if it cannot be measured or is changing over time. Using this method, stable fixed points can be distinguished from ghost attractors in the presence of noise, networks with similar phase but different underlying dynamics can be resolved, and the movement of stable fixed points can be observed. The time-series vector method is a valuable tool for distinguishing dynamics and describing robustness. It can be adapted for use in larger populations and non-reciprocal circuits. Finally, some larger implications of neuroscience research, specifically the use of neural interfaces for national security, are discussed. Neural interfaces for human enhancement in a national security context raise a number of unique ethical and policy concerns not common to dual use research of concern or traditional human subjects research. Guidelines about which technologies should be developed are lacking. We discuss a two-step framework with 1) an initial screen to prioritize technologies that should be reviewed immediately, and 2) a comprehensive ethical review regarding concerns for the enhanced individual, operational norms, and multi-use applications in the case of transfer to civilian contexts.Georgia Institute of TechnologyButera, Robert J.2016-01-07T17:21:10Z2016-01-07T17:21:10Z2014-122014-08-22December 20142016-01-07T17:21:10ZDissertationapplication/pdfhttp://hdl.handle.net/1853/54269en_US
collection NDLTD
language en_US
format Others
sources NDLTD
topic Phase resetting curve
Neurons
Variability
Computational neuroscience
Electrophysiology
spellingShingle Phase resetting curve
Neurons
Variability
Computational neuroscience
Electrophysiology
Norman, Sharon Elizabeth
Quantifying dynamics and variability in neural systems
description Synchronized neural activity, in which the firing of neurons is coordinated in time, is an observed phenomenon in many neural functions. The conditions that promote synchrony and the dynamics of synchronized activity are active areas of investigation because they are incompletely understood. In addition, variability is intrinsic to biological systems, but the effect of neuron spike time variability on synchronization dynamics is a question that merits more attention. Previous experiments using a hybrid circuit of one biological neuron coupled to one computational neuron revealed that irregularity in biological neuron spike timing could change synchronization in the circuit, transitioning the activity between phase-locked and phase slipping. Simulations of this circuit could not replicate the transitions in network activity if neuron period was represented as a Gaussian process, but could if a process with history and a stochastic component were used. The phase resetting curve (PRC), which describes how neuron cycles change in response to input, can be used to construct a map that predicts if synchronization will occur in hybrid circuits. Without modification, these maps did not always capture observed network activity. I conducted long-term recordings of invertebrate neurons and show that interspike interval (ISI) can be represented as an autoregressive integrated moving average process, where ISI is dependent on past history and a stochastic component with history. Using integrate and fire model simulations, I suggest that stochastic activity in adaptation channels could be responsible for the history dependence and correlational structure observed in these neurons. This evidence for stochastic, history-dependent noise in neural systems indicates that our understanding of network dynamics could be enhanced by including more complex, but relevant, forms of noise. I show that cycle-by-cycle dynamics of the coupled system can be used to infer features of the dynamic map, even if it cannot be measured or is changing over time. Using this method, stable fixed points can be distinguished from ghost attractors in the presence of noise, networks with similar phase but different underlying dynamics can be resolved, and the movement of stable fixed points can be observed. The time-series vector method is a valuable tool for distinguishing dynamics and describing robustness. It can be adapted for use in larger populations and non-reciprocal circuits. Finally, some larger implications of neuroscience research, specifically the use of neural interfaces for national security, are discussed. Neural interfaces for human enhancement in a national security context raise a number of unique ethical and policy concerns not common to dual use research of concern or traditional human subjects research. Guidelines about which technologies should be developed are lacking. We discuss a two-step framework with 1) an initial screen to prioritize technologies that should be reviewed immediately, and 2) a comprehensive ethical review regarding concerns for the enhanced individual, operational norms, and multi-use applications in the case of transfer to civilian contexts.
author2 Butera, Robert J.
author_facet Butera, Robert J.
Norman, Sharon Elizabeth
author Norman, Sharon Elizabeth
author_sort Norman, Sharon Elizabeth
title Quantifying dynamics and variability in neural systems
title_short Quantifying dynamics and variability in neural systems
title_full Quantifying dynamics and variability in neural systems
title_fullStr Quantifying dynamics and variability in neural systems
title_full_unstemmed Quantifying dynamics and variability in neural systems
title_sort quantifying dynamics and variability in neural systems
publisher Georgia Institute of Technology
publishDate 2016
url http://hdl.handle.net/1853/54269
work_keys_str_mv AT normansharonelizabeth quantifyingdynamicsandvariabilityinneuralsystems
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