Poster No:
2155
Submission Type:
Abstract Submission
Authors:
Anna Behler1, Nikitas Koussis2, Michael Breakspear3
Institutions:
1University of Newcastle, Callaghan, NSW, 2University of Newcastle, New Lambton Heights, New South Wales, 3University of Newcastle, Newcastle, N/A
First Author:
Co-Author(s):
Nikitas Koussis
University of Newcastle
New Lambton Heights, New South Wales
Introduction:
Dynamic interactions between subcortical structures and cortical regions are essential to the execution of cognitive functions. In particular, the relationship between the hippocampus and cortex is vital for memory encoding and retrieval (Ren et al., 2018), with both structures demonstrating oscillatory activity marked by propagation of traveling waves (Roberts et al., 2019; Zhang & Jacobs, 2015). As the understanding of wave-wave interactions underlying the integration of these two brain areas is limited, this study focuses on investigating hippocampal waves and their interactions with the cortex computationally, aiming to develop models of these interactions that yield testable predictions.
Methods:
Biophysically informed non-linear neural mass models (i.e., Jansen-Rit columns) were used to simulate neural activity on a hippocampal mesh and a cortical representation. The coupled models of both brain areas were subjected to parameter sweeps and perturbation analyses to characterize global coherence, phase velocity and to identify preferred wave propagation patterns in the models. Different coupling mechanism between the hippocampus and cortex were then investigated.
Results:
A small gradient in external input is crucial for the emergence of traveling waves in the hippocampus, yielding a clear preference for wave directions following the antero-posterior spatial gradient. The nodal phase velocity can be adjusted by tuning the magnitude of the gradient of the external input, i.e. the difference between minimum and maximum of external input; yielding velocities between 0.5 and 2 m/s. Intricate wave interactions, with phase-phase relationships, arose through coupling the hippocampal to the cortex. The nature of these interactions was substantially impacted by the chosen inter-system coupling configuration, including one-to-one, sparse, or clustered coupling schemes. Furthermore, the ratio of inter-system to intra-system coupling strength plays a crucial role in shaping these interactions.

·A) Snapshot of pyramidal post synaptic potential, B) of nodal phase velocity vectors, and C) streamlines at 5 s after start of the simulation indicating the presence of a wave traveling.
Conclusions:
These computational analyses offer detailed mechanistic insights into how traveling waves of neural activity form in the hippocampus and how wave-wave interactions can contribute to cortico-hippocampal functioning. Notably, the hippocampal model fits the wave velocity for slow theta oscillations, aligning with detailed neurophysiological recordings (Zhang & Jacobs, 2015). In sum, the models provide hypotheses that can be directly tested using neuroimaging data from intracranial EEG, such as in epilepsy patients performing cognitive tasks, thereby contributing to a translational neuroscience approach.
By providing testable computational models, our study builds a robust framework for understanding cortico-hippocampal interactions and has significant implications for future research in cognitive neuroscience and neurodegenerative disorders associated with memory dysfunctions.
Modeling and Analysis Methods:
Other Methods 2
Neuroanatomy, Physiology, Metabolism and Neurotransmission:
Subcortical Structures 1
Keywords:
Computational Neuroscience
Cortical Columns
Modeling
Sub-Cortical
Other - Hippocampus
1|2Indicates the priority used for review
Provide references using author date format
Ren, Y., Nguyen, V. T., Sonkusare, S., Lv, J., Pang, T., Guo, L., Eickhoff, S. B., Breakspear, M., & Guo, C. C. (2018). Effective connectivity of the anterior hippocampus predicts recollection confidence during natural memory retrieval. Nature Communications, 9(1), 4875. https://doi.org/10.1038/s41467-018-07325-4
Roberts, J. A., Gollo, L. L., Abeysuriya, R. G., Roberts, G., Mitchell, P. B., Woolrich, M. W., & Breakspear, M. (2019). Metastable brain waves. Nature Communications, 10(1), 1056. https://doi.org/10.1038/s41467-019-08999-0
Zhang, H., & Jacobs, J. (2015). Traveling Theta Waves in the Human Hippocampus. Journal of Neuroscience, 35(36), 12477–12487. https://doi.org/10.1523/JNEUROSCI.5102-14.2015