Poster No:
1674
Submission Type:
Abstract Submission
Authors:
Shih-Cheng Chien1, Stanislav Jiříček2, Thomas Knösche3, Jaroslav Hlinka2, Helmut Schmidt1
Institutions:
1Institute of Computer Science, The Czech Academy of Sciences, Prague, Prague, 2Institute of Computer Science of the Czech Academy of Sciences, Prague, Czech Republic, 3Max Planck Institute, Leipzig, Saxony
First Author:
Shih-Cheng Chien
Institute of Computer Science, The Czech Academy of Sciences
Prague, Prague
Co-Author(s):
Stanislav Jiříček
Institute of Computer Science of the Czech Academy of Sciences
Prague, Czech Republic
Jaroslav Hlinka
Institute of Computer Science of the Czech Academy of Sciences
Prague, Czech Republic
Helmut Schmidt
Institute of Computer Science, The Czech Academy of Sciences
Prague, Prague
Introduction:
Studies investigating the relationship between electrophysiology (EEG) rhythms and blood-oxygen-level-dependent (BOLD) activity have revealed intriguing correlations, such as the negative correlation between EEG alpha power and BOLD signal in occipital areas during eyes-closed resting states. Conversely, positive correlations have been observed in various other brain regions [1]. Additionally, studies have identified positive correlations between EEG gamma power and the BOLD signal during sensory stimulation [2]. A possible interpretation for these diverse findings may lie in the involvement of distinct types of inhibitory neurons, known for their differential effects on EEG rhythm generation [3] and varied neural-vascular coupling properties [4].
Methods:
This study employs a cortical column model to simulate EEG and BOLD signals, encompassing excitatory (E) and inhibitory (PV, SOM, and VIP) populations across cortical layers (L2/3, L4, and L5/6). Various conditions are simulated, with the model initially driven by constant inputs to induce either PV-dominant or SOM-dominant states [5]. Subsequently, a combination of pink noises serves as thalamic input (to E and PV populations) and cortico-cortical input (to E populations). The EEG signals are approximated by the weighted sum of simulated excitatory and inhibitory postsynaptic potentials (EPSPs and IPSPs) of the E populations. BOLD signals are simulated using the Balloon-Windkessel model [6], where the input is the sum of simulated EPSPs of the E, PV, SOM, and VIP populations. Simulated EEGs and BOLDs undergo typical analysis procedures employed in investigating the EEG-BOLD relationship in experimental studies.
Results:
In the PV-dominant state, our simulations reveal a positive correlation between the EEG and BOLD signals, denoted by a significant correlation coefficient. Conversely, the simulated EEG and BOLD signals exhibit a negative correlation under the SOM-dominant state. These findings highlight the influence of inhibitory neuron dominance on the observed correlation patterns between EEG and BOLD signals.
Conclusions:
This preliminary exploration delves into the potential factors contributing to the observed (anti-)correlation between EEG and BOLD signals in EEG-fMRI experiments. We identify instances that give rise to the observed anti/correlation phenomena by systematically examining model configurations across the parameter space. These configurations are linked to dynamic factors, such as variations in input sets, and static factors, including intra-column connectivity and the ratio of PV/SOM cell counts. The nuanced interplay of these factors provides valuable insights for future investigations into the underlying dynamic columnar states in simultaneous EEG/fMRI studies.
Modeling and Analysis Methods:
EEG/MEG Modeling and Analysis 1
fMRI Connectivity and Network Modeling
Task-Independent and Resting-State Analysis 2
Keywords:
Cerebral Blood Flow
Computational Neuroscience
Cortex
Cortical Columns
Cortical Layers
Electroencephaolography (EEG)
FUNCTIONAL MRI
Modeling
1|2Indicates the priority used for review
Provide references using author date format
[1] Gonçalves, Sonia I. (2006), 'Correlating the alpha rhythm to BOLD using simultaneous EEG/fMRI: inter-subject variability', Neuroimage 30.1, 203-213.
[2] Niessing, Jorn (2005), 'Hemodynamic signals correlate tightly with synchronized gamma oscillations', science 309.5736, 948-951.
[3] Whittington, Miles A. (2003), 'Interneuron diversity series: inhibitory interneurons and network oscillations in vitro', Trends in neurosciences 26.12, 676-682.
[4] Cauli, Bruno (2004), 'Cortical GABA interneurons in neurovascular coupling: relays for subcortical vasoactive pathways', Journal of Neuroscience 24.41, 8940-8949.
[5] Hertäg, Loreen (2019), 'Amplifying the redistribution of somato-dendritic inhibition by the interplay of three interneuron types', PLoS computational biology 15.5, e1006999.
[6] Friston, Karl J. (2000), 'Nonlinear responses in fMRI: the Balloon model, Volterra kernels, and other hemodynamics', NeuroImage 12.4, 466-477.