Analysis of hippocampal local field potentials by diffusion mapped delay coordinates
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Published:2024-04-06
Issue:2
Volume:52
Page:133-144
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ISSN:0929-5313
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Container-title:Journal of Computational Neuroscience
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language:en
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Short-container-title:J Comput Neurosci
Author:
Gonzalez D. A.,Peel J. H.,Pagadala T.,McHail D. G.,Cressman J. R.,Dumas T. C.
Abstract
AbstractSpatial navigation through novel spaces and to known goal locations recruits multiple integrated structures in the mammalian brain. Within this extended network, the hippocampus enables formation and retrieval of cognitive spatial maps and contributes to decision making at choice points. Exploration and navigation to known goal locations produce synchronous activity of hippocampal neurons resulting in rhythmic oscillation events in local networks. Power of specific oscillatory frequencies and numbers of these events recorded in local field potentials correlate with distinct cognitive aspects of spatial navigation. Typically, oscillatory power in brain circuits is analyzed with Fourier transforms or short-time Fourier methods, which involve assumptions about the signal that are likely not true and fail to succinctly capture potentially informative features. To avoid such assumptions, we applied a method that combines manifold discovery techniques with dynamical systems theory, namely diffusion maps and Takens’ time-delay embedding theory, that avoids limitations seen in traditional methods. This method, called diffusion mapped delay coordinates (DMDC), when applied to hippocampal signals recorded from juvenile rats freely navigating a Y-maze, replicates some outcomes seen with standard approaches and identifies age differences in dynamic states that traditional analyses are unable to detect. Thus, DMDC may serve as a suitable complement to more traditional analyses of LFPs recorded from behaving subjects that may enhance information yield.
Funder
National Institutes of Health
Publisher
Springer Science and Business Media LLC
Reference22 articles.
1. Berry, T., Cressman, J., Gregurić-Ferenček, Z., & andSauer T. (2013). Time-scale separation from diffusion-mapped delay coordinates. SIAM Journal on Applied Dynamical Systems [Electronic Only]. https://doi.org/10.1137/12088183X 2. Blair, M. G., Nguyen, N.-Q., Albani, S. H., L’Etoile, M. M., Andrawis, M. M., Owen, L. M., Oliveira, R. F., et al. (2013). Developmental changes in structural and functional properties of hippocampal AMPARs parallels the emergence of deliberative spatial navigation in Juvenile Rats. Journal of Neuroscience, 33(30), 12218–12228. https://doi.org/10.1523/JNEUROSCI.4827-12.2013 3. Buzsáki, G., Buhl, D. L., Harris, K. D., Csicsvari, J., Czéh, B., & Morozov, A. (2003). Hippocampal network patterns of activity in the mouse. Neuroscience, 116(1), 201–211. https://doi.org/10.1016/s0306-4522(02)00669-3 4. Cabral, J., Luckhoo, H., Woolrich, M., Joensson, M., Mohseni, H., Baker, A., Kringelbach, M. L., & Deco, G. (2014). Exploring Mechanisms of Spontaneous Functional Connectivity in MEG: How delayed network interactions lead to structured amplitude envelopes of band-pass filtered oscillations. NeuroImage, 90(April), 423–435. https://doi.org/10.1016/j.neuroimage.2013.11.047 5. Carr, M. F., Karlsson, M. P., & Frank, L. M. (2012). Transient slow gamma synchrony underlies hippocampal memory replay. Neuron, 75, 700–713.
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