Category: Neural Basis of Navigation

How the hippocampus-accumbens code guides goal-directed appetitive behavior?

Oliver Barnstedt, Petra Mocellin, Stefan Remy. A hippocampus-accumbens code guides goal-directed appetitive behavior. bioRxiv 2023.03.09.531869; doi: https://doi.org/10.1101/2023.03.09.531869

Abstract
Neurons in dorsal hippocampus (dHPC) encode a rich repertoire of task-relevant environmental features, while downstream regions such as the …

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How human visual area V6 transforms spatially relevant sensory information into an egocentric representation for navigation?

Aggius-Vella E, Chebat DR, Maidenbaum S, Amedi A. Activation of human visual area V6 during egocentric navigation with and without visual experience. Current Biology. 2023 Mar 1.

Summary
V6 is a retinotopic area located in the dorsal visual

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How the neural representation of allocentric space is distorted by goal-directed behaviour?

PS Muhle-Karbe, H Sheahan, G Pezzulo, HJ Spiers, S Chien, NW Schuck, C Summerfield. Goal-seeking compresses neural codes for space in the human hippocampus and orbitofrontal cortex. bioRxiv 2023.01.12.523762; doi: https://doi.org/10.1101/2023.01.12.523762

Abstract
Humans can navigate flexibly to meet

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How the brain process gated transformations from egocentric to allocentric reference frames involving retrosplenial cortex, entorhinal cortex, and hippocampus?

Alexander, A. S., Robinson, J. C., Stern, C. E., & Hasselmo, M. E. (2023). Gated transformations from egocentric to allocentric reference frames involving retrosplenial cortex, entorhinal cortex, and hippocampus. Hippocampus, 1– 23. https://doi.org/10.1002/hipo.23513

Abstract
This paper reviews the

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What’s the local circuit-basis for spatial navigation and memory processes in hippocampal area CA1?

Tristan Geiller, James B. Priestley, Attila Losonczy. A local circuit-basis for spatial navigation and memory processes in hippocampal area CA1. Current Opinion in Neurobiology. Volume 79, 2023,102701.

Abstract
“The hippocampus is a multi-stage neural circuit that is critical for …

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How lateral oscillations are produced and participate in visual navigation for insects?

Leo Clement, Sebastian Schwarz, Antoine Wystrach. An intrinsic oscillator underlies visual navigation in ants. Current Biology, Volume 33, Issue 3, 2023, Pages 411-422.e5. 

Summary
Many insects display lateral oscillations while moving, but how these oscillations are produced and

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How brain encode object-location memories?

Yusuke Teratani-Ota, Brian J. Wiltgen. Encoding object-location memories along the proximodistal axis of CA1. bioRxiv 2022.10.17.512601; doi: https://doi.org/10.1101/2022.10.17.512601

Abstract
The hippocampus is thought to combine “what” and “where” information from the cortex so that objects and events can

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How rat brain transform egocentric views into goal-directed navigation behavior?

LaChance, Patrick A., and Jeffrey S. Taube. “A model for transforming egocentric views into goal‐directed behavior.” Hippocampus (2023).

Abstract

Neurons in the rat postrhinal cortex (POR) respond to the egocentric (observer-centered) bearing and distance of the boundaries,

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How the brain maintain and update the uncertainty about one’s location to navigate efficiently?

Yul HR Kang, Daniel M Wolpert, Máté Lengyel. Spatial uncertainty and environmental geometry in navigation. bioRxiv 2023.01.30.526278; doi: https://doi.org/10.1101/2023.01.30.526278

Abstract
Variations in the geometry of the environment, such as the shape and size of an enclosure, have profound

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How entorhinal grid-like codes and time-locked network dynamics track others navigating through space?

Isabella C. Wagner, Luise P. Graichen, Boryana Todorova, Andre Lüttig, David B. Omer, Matthias Stangl & Claus Lamm. Entorhinal grid-like codes and time-locked network dynamics track others navigating through space. Nat Commun 14, 231 (2023). https://doi.org/10.1038/s41467-023-35819-3

Abstract
Navigating

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How causal inference is performed in attributing retinal motion to self- and object-motion during closed-loop goal-directed navigation?

Jean-Paul Noel, Johannes Bill, Haoran Ding, John Vastola, Gregory C DeAngelis, Dora Angelaki, Jan Drugowitsch. Causal inference during closed-loop navigation: parsing of self- and object-motion. bioRxiv 2023.01.27.525974; doi: https://doi.org/10.1101/2023.01.27.525974

Abstract
A key computation in building adaptive internal models

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How the human brain is tuned to veridical head direction signals?

Benjamin J Griffiths, Thomas Schreiner, Julia Schaefer, Christian Vollmar, Elisabeth Kaufmann, Stefanie Quach, Jan Remi, Soheyl Noachtar, Tobias Staudigl. Electrophysiological signatures of veridical head direction in humans. bioRxiv 2023.01.26.525724; doi: https://doi.org/10.1101/2023.01.26.525724

Abstract
“Information about heading direction is critical for …

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How navigation and memory processes interact in humans?

Thomas Schreiner, Benjamin J. Griffiths, Merve Kutlu, Christian Vollmar, Elisabeth Kaufmann, Stefanie Quach, Jan Remi, Soheyl Noachtar, Tobias Staudigl. Memory reactivation of real-world spatial orientation revealed by human electrophysiology. bioRxiv 2023.01.27.525854; doi: https://doi.org/10.1101/2023.01.27.525854

Abstract
Spatial navigation and memory

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How retrosplenial cortex computes heading direction from landmark information?

Eleonora Lomi, Kate Jeffery, Anna Mitchell. Convergence of direction, location and theta in the rat anteroventral thalamic nucleus. bioRxiv 2023.01.11.523585; doi: https://doi.org/10.1101/2023.01.11.523585

Abstract
Retrosplenial cortex (RSC) is a cortical region that computes heading direction from landmark information, but

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How the hippocampus incorporates new contextual information into a previously formed and stabilized spatial representation?

Jake Ormond, Simon A. Serka, Joshua P. Johansen. Enhanced reactivation of remapping place cells during aversive learning. Journal of Neuroscience 3 January 2023, JN-RM-1450-22; DOI: 10.1523/JNEUROSCI.1450-22.2022

Abstract
Study of the hippocampal place cell system has greatly enhanced our

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