Neural Adaptation and Fractional Dynamics as a Window to Underlying Neural Excitability

Author:

Lundstrom Brian N.ORCID,Richner Tom

Abstract

AbstractThe relationship between macroscale electrophysiological recordings and the dynamics of underlying neural activity remains unclear. We have previously shown that low frequency EEG activity (<1 Hz) is decreased at the seizure onset zone (SOZ), while higher frequency activity (1-50 Hz) is increased. These changes result in power spectral densities (PSDs) with flattened slopes near the SOZ, which are assumed to be areas of increased excitability. We wanted to understand possible mechanisms underlying PSD changes in brain regions of increased excitability. We hypothesize that these observations are consistent with changes in adaptation within the neural circuit.We developed a theoretical framework and tested the effect of adaptation mechanisms, such as spike frequency adaptation and synaptic depression, on excitability and PSDs using filter-based neural mass models and conductance-based models. We compared the contribution of single timescale adaptation and multiple timescale adaptation.We found that adaptation with multiple timescales alters the PSDs. Multiple timescales of adaptation can approximate fractional dynamics, a form of calculus related to power laws, history dependence, and non-integer order derivatives. Coupled with input changes, these dynamics changed circuit responses in unexpected ways. Increased input without synaptic depression increases broadband power. However, increased input with synaptic depression may decrease power. The effects of adaptation were most pronounced for low frequency activity (< 1Hz). Increased input combined with a loss of adaptation yielded reduced low frequency activity and increased higher frequency activity, consistent with clinical EEG observations from SOZs.Spike frequency adaptation and synaptic depression, two forms of multiple timescale adaptation, affect low frequency EEG and the slope of PSDs. These neural mechanisms may underlie changes in EEG activity near the SOZ and relate to neural hyperexcitability. Neural adaptation may be evident in macroscale electrophysiological recordings and provide a window to understanding neural circuit excitability.Author SummaryElectrophysiological recordings such as EEG from the human brain often come from many thousands of neurons or more. It can be difficult to relate recorded activity to characteristics of the underlying neurons and neural circuits. Here, we use novel theoretical framework and computational neural models to understand how neural adaptation might be evident in human EEG recordings. Neural adaptation includes mechanisms such as spike frequency adaptation and short-term depression that emphasize stimulus changes and help promote stability. Our results suggest that changes in neural adaptation affect EEG signals, especially at low frequencies. Further, adaptation can lead to changes related to fractional derivatives, a kind of calculus with non-integer orders. Neural adaptation may provide a window into understanding specific aspects of neuron excitability even from EEG recordings.

Publisher

Cold Spring Harbor Laboratory

Reference43 articles.

1. Trappenberg TP. Fundamentals of Computational Neuroscience. Oxford University Press, USA; 2002. 360 p.

2. Dayan P , Abbott LF. Theoretical neuroscience: computational and mathematical modeling of neural systems [Internet]. Cambridge, Mass.: Massachusetts Institute of Technology Press; 2001. xv, 460 p. p. (Computational neuroscience). Available from: http://www.loc.gov/catdir/toc/fy031/2001044005.html

3. Kandel ER , Schwartz JH , Jessell TM , Siegelbaum SA , Hudspeth AJ , editors. Principles of Neural Science. 5th edition. New York: McGraw-Hill Professional Pub; 2012. 1760 p.

4. Sensory adaptation

5. Distributed Relaxation Processes in Sensory Adaptation

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