TY - JOUR
T1 - Impact of DC-Coupled Electrophysiological Recordings for Translational Neuroscience
T2 - Case Study of Tracking Neural Dynamics in Rodent Models of Seizures
AU - Jafarian, Amirhossein
AU - Wykes, Rob C
N1 - Funding Information:
RW is funded by a Senior Research Fellowship awarded by the Worshipful Company of Pewterers. This work has received funding from the European Union's Horizon 2020 research and innovation programme under Grant Agreement No 881603 (GrapheneCore3).
Publisher Copyright:
Copyright © 2022 Jafarian and Wykes.
PY - 2022/7/21
Y1 - 2022/7/21
N2 - We propose that to fully understand biological mechanisms underlying pathological brain activity with transitions (e.g., into and out of seizures), wide-bandwidth electrophysiological recordings are important. We demonstrate the importance of ultraslow potential shifts and infraslow oscillations for reliable tracking of synaptic physiology, within a neural mass model, from brain recordings that undergo pathological phase transitions. We use wide-bandwidth data (direct current (DC) to high-frequency activity), recorded using epidural and penetrating graphene micro-transistor arrays in a rodent model of acute seizures. Using this technological approach, we capture the dynamics of infraslow changes that contribute to seizure initiation (active pre-seizure DC shifts) and progression (passive DC shifts). By employing a continuous-discrete unscented Kalman filter, we track biological mechanisms from full-bandwidth data with and without active pre-seizure DC shifts during paroxysmal transitions. We then apply the same methodological approach for tracking the same parameters after application of high-pass-filtering >0.3Hz to both data sets. This approach reveals that ultraslow potential shifts play a fundamental role in the transition to seizure, and the use of high-pass-filtered data results in the loss of key information in regard to seizure onset and termination dynamics.
AB - We propose that to fully understand biological mechanisms underlying pathological brain activity with transitions (e.g., into and out of seizures), wide-bandwidth electrophysiological recordings are important. We demonstrate the importance of ultraslow potential shifts and infraslow oscillations for reliable tracking of synaptic physiology, within a neural mass model, from brain recordings that undergo pathological phase transitions. We use wide-bandwidth data (direct current (DC) to high-frequency activity), recorded using epidural and penetrating graphene micro-transistor arrays in a rodent model of acute seizures. Using this technological approach, we capture the dynamics of infraslow changes that contribute to seizure initiation (active pre-seizure DC shifts) and progression (passive DC shifts). By employing a continuous-discrete unscented Kalman filter, we track biological mechanisms from full-bandwidth data with and without active pre-seizure DC shifts during paroxysmal transitions. We then apply the same methodological approach for tracking the same parameters after application of high-pass-filtering >0.3Hz to both data sets. This approach reveals that ultraslow potential shifts play a fundamental role in the transition to seizure, and the use of high-pass-filtered data results in the loss of key information in regard to seizure onset and termination dynamics.
KW - DC-coupled electrophysiological recordings
KW - continuous-discrete unscented Kalman filter
KW - infraslow oscillations
KW - neural mass model
KW - synaptic physiology
U2 - 10.3389/fncom.2022.900063
DO - 10.3389/fncom.2022.900063
M3 - Article
C2 - 35936824
SN - 1662-5188
VL - 16
JO - Frontiers in Computational Neuroscience
JF - Frontiers in Computational Neuroscience
M1 - 900063
ER -