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Neurodegeneration exposes firing rate dependent effects on oscillation dynamics in computational neural networks
by
Schumm, Samantha
, Parvesse, Brandon
, Meaney, David F
, Gabrieli, David
in
Bioengineering
/ Computational neuroscience
/ Cortex
/ Firing pattern
/ Firing rate
/ Neural networks
/ Neurodegeneration
/ Neurons
/ Neuroplasticity
/ Oscillations
/ Rhythms
/ Traumatic brain injury
2019
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Neurodegeneration exposes firing rate dependent effects on oscillation dynamics in computational neural networks
by
Schumm, Samantha
, Parvesse, Brandon
, Meaney, David F
, Gabrieli, David
in
Bioengineering
/ Computational neuroscience
/ Cortex
/ Firing pattern
/ Firing rate
/ Neural networks
/ Neurodegeneration
/ Neurons
/ Neuroplasticity
/ Oscillations
/ Rhythms
/ Traumatic brain injury
2019
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Do you wish to request the book?
Neurodegeneration exposes firing rate dependent effects on oscillation dynamics in computational neural networks
by
Schumm, Samantha
, Parvesse, Brandon
, Meaney, David F
, Gabrieli, David
in
Bioengineering
/ Computational neuroscience
/ Cortex
/ Firing pattern
/ Firing rate
/ Neural networks
/ Neurodegeneration
/ Neurons
/ Neuroplasticity
/ Oscillations
/ Rhythms
/ Traumatic brain injury
2019
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Neurodegeneration exposes firing rate dependent effects on oscillation dynamics in computational neural networks
Paper
Neurodegeneration exposes firing rate dependent effects on oscillation dynamics in computational neural networks
2019
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Overview
Traumatic brain injury (TBI) can lead to neurodegeneration in the injured circuitry, either through primary structural damage to the neuron or secondary effects that disrupt key cellular processes. Moreover, traumatic injuries can preferentially impact subpopulations of neurons, but the functional network effects of these targeted degeneration profiles remain unclear. Although isolating the consequences of complex injury dynamics and long-term recovery of the circuit can be difficult to control experimentally, computational networks can be a powerful tool to analyze the consequences of injury. Here, we use the Izhikevich spiking neuron model to create networks representative of cortical tissue. After an initial settling period with spike-timing-dependent plasticity (STDP), networks developed rhythmic oscillations similar to those seen in vivo. As neurons were sequentially removed from the network, population activity rate and oscillation dynamics were significantly reduced. In a successive period of network restructuring with STDP, network activity levels were returned to baseline for some injury levels and oscillation dynamics significantly improved. We next explored the role that specific neurons have in the creation and termination of oscillation dynamics. We determined that oscillations initiate from activation of low firing rate neurons with limited structural inputs. To terminate oscillations, high activity excitatory neurons with strong input connectivity activate downstream inhibitory circuitry. Finally, we confirm the excitatory neuron population role through targeted neurodegeneration. These results suggest targeted neurodegeneration can play a key role in the oscillation dynamics after injury.
Publisher
Cold Spring Harbor Laboratory Press,Cold Spring Harbor Laboratory
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