All Relations between representation and hippocampus

Publication Sentence Publish Date Extraction Date Species
Stephanie L Grella, Tia N Donaldso. Contextual memory engrams, and the neuromodulatory influence of the locus coeruleus. Frontiers in molecular neuroscience. vol 17. 2024-02-20. PMID:38375501. we then outline a recent hypothesis involving noradrenergic and dopaminergic projections from the locus coeruleus (lc) to different subregions of the hippocampus, in sculpting contextual representations, giving a brief description of the neuroanatomical and physiological properties of the lc. 2024-02-20 2024-02-22 Not clear
Laurenz Muessig, Fabio Ribeiro Rodrigues, Tale L Bjerknes, Benjamin W Towse, Caswell Barry, Neil Burgess, Edvard I Moser, May-Britt Moser, Francesca Cacucci, Thomas J Will. Environment geometry alters subiculum boundary vector cell receptive fields in adulthood and early development. Nature communications. vol 15. issue 1. 2024-02-01. PMID:38302455. however, subiculum and entorhinal bvc receptive fields are altered by boundary geometry as early as tested, suggesting this is an inherent feature of the hippocampal representation of space. 2024-02-01 2024-02-04 rat
César Torres-Morales, Selene Cansin. Brain representations of space and time in episodic memory: A systematic review and meta-analysis. Cognitive, affective & behavioral neuroscience. vol 24. issue 1. 2024-01-30. PMID:38030912. the hippocampus is the main brain region involved in processing spatial and temporal information for incorporation within episodic memory representations. 2024-01-30 2024-02-01 Not clear
Nakul Yadav, Andrew Toader, Priya Rajasethupath. Beyond hippocampus: Thalamic and prefrontal contributions to an evolving memory. Neuron. 2024-01-25. PMID:38272026. by synthesizing studies across the rodent and human literature, we suggest that as memory representations initially form in hippocampus, parallel traces emerge in frontal cortex that cue memory recall, and as they mature, with sustained support initially from limbic then diencephalic then cortical circuits, they become progressively independent of hippocampus and dependent on a mature cortical representation. 2024-01-25 2024-01-28 human
Yohan J John, Jingyi Wang, Daniel Bullock, Helen Barba. Amygdalar Excitation of Hippocampal Interneurons Can Lead to Emotion-driven Overgeneralization of Context. Journal of cognitive neuroscience. 2024-01-23. PMID:38261402. our model revealed an elegant circuit mechanism that mediates an affective "inverted u" phenomenonv: there is an optimal level of amygdalar input that enriches hippocampal context representations, but on either side of this zone, representations are impoverished. 2024-01-23 2024-01-25 Not clear
Ian Cone, Claudia Clopat. Latent representations in hippocampal network model co-evolve with behavioral exploration of task structure. Nature communications. vol 15. issue 1. 2024-01-23. PMID:38263408. latent representations in hippocampal network model co-evolve with behavioral exploration of task structure. 2024-01-23 2024-01-26 Not clear
Ian Cone, Claudia Clopat. Latent representations in hippocampal network model co-evolve with behavioral exploration of task structure. Nature communications. vol 15. issue 1. 2024-01-23. PMID:38263408. the hippocampus is known to develop representations of this complex structure, forming a so-called "cognitive map". 2024-01-23 2024-01-26 Not clear
Eleanor Spens, Neil Burges. A generative model of memory construction and consolidation. Nature human behaviour. 2024-01-19. PMID:38242925. here we present a computational model in which hippocampal replay (from an autoassociative network) trains generative models (variational autoencoders) to (re)create sensory experiences from latent variable representations in entorhinal, medial prefrontal and anterolateral temporal cortices via the hippocampal formation. 2024-01-19 2024-01-22 Not clear
Kate J Jeffer. The mosaic structure of the mammalian cognitive map. Learning & behavior. 2024-01-17. PMID:38231426. the subsequent discovery of place cells in the hippocampus of rats suggested that such a map-like representation does exist, and also provided a tool with which to explore its properties. 2024-01-17 2024-01-19 rat
Justin D Shin, Shantanu P Jadha. Cortical ripples mediate top-down suppression of hippocampal reactivation during sleep memory consolidation. bioRxiv : the preprint server for biology. 2024-01-03. PMID:38168420. consolidation of initially encoded hippocampal representations in the neocortex through reactivation is crucial for long-term memory formation, and is facilitated by the coordination of hippocampal sharp-wave ripples (swrs) with cortical oscillations during non-rem sleep. 2024-01-03 2024-01-06 Not clear
Runnan Cao, Jinge Wang, Peter Brunner, Jon T Willie, Xin Li, Ueli Rutishauser, Nicholas J Brandmeir, Shuo Wan. Neural mechanisms of face familiarity and learning in the human amygdala and hippocampus. Cell reports. 2023-12-27. PMID:38151023. here, we record from single neurons in the human amygdala and hippocampus and find a greater neuronal representational distance between pairs of familiar faces than unfamiliar faces, suggesting that neural representations for familiar faces are more distinct. 2023-12-27 2023-12-30 human
Marta Boscaglia, Chiara Gastaldi, Wulfram Gerstner, Rodrigo Quian Quirog. A dynamic attractor network model of memory formation, reinforcement and forgetting. PLoS computational biology. vol 19. issue 12. 2023-12-20. PMID:38117859. empirical evidence shows that memories that are frequently revisited are easy to recall, and that familiar items involve larger hippocampal representations than less familiar ones. 2023-12-20 2023-12-23 Not clear
Usman Farooq, George Drago. Geometric experience sculpts the development and dynamics of hippocampal sequential cell assemblies. bioRxiv : the preprint server for biology. 2023-12-18. PMID:38105999. thus, early-life experience with euclidean geometry enriches the hippocampal repertoire of preconfigured neuronal patterns selected toward unique representation and discrimination of multiple linear environments. 2023-12-18 2023-12-21 rat
Kailong Peng, Jeffrey D Wammes, Alex Nguyen, Marius Cătălin Iordan, Kenneth A Norman, Nicholas B Turk-Brown. Inducing representational change in the hippocampus through real-time neurofeedback. bioRxiv : the preprint server for biology. 2023-12-18. PMID:38106228. these changes can reflect increased (integration) or decreased (differentiation) overlap; previous studies have posited that the amount of coactivation between competing representations in cortex determines which will occur: high coactivation leads to hippocampal integration, medium coactivation leads to differentiation, and low coactivation is inert. 2023-12-18 2023-12-21 human
Kailong Peng, Jeffrey D Wammes, Alex Nguyen, Marius Cătălin Iordan, Kenneth A Norman, Nicholas B Turk-Brown. Inducing representational change in the hippocampus through real-time neurofeedback. bioRxiv : the preprint server for biology. 2023-12-18. PMID:38106228. such behavioral consequences result from changes in how much the neural representations of the items overlap, especially in the hippocampus. 2023-12-18 2023-12-21 human
Shenyang Huang, Cortney M Howard, Mariam Hovhannisyan, Maureen Ritchey, Roberto Cabeza, Simon W Davi. Hippocampal functions modulate transfer-appropriate cortical representations supporting subsequent memory. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2023-12-05. PMID:38050089. hippocampal functions modulate transfer-appropriate cortical representations supporting subsequent memory. 2023-12-05 2023-12-10 human
Shenyang Huang, Cortney M Howard, Mariam Hovhannisyan, Maureen Ritchey, Roberto Cabeza, Simon W Davi. Hippocampal functions modulate transfer-appropriate cortical representations supporting subsequent memory. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2023-12-05. PMID:38050089. representational similarity analysis revealed robust representations of visual and semantic information in canonical visual (e.g., occipital cortex) and semantic (e.g., angular gyrus) regions in the cortex, but not in the hippocampus. 2023-12-05 2023-12-10 human
Shenyang Huang, Cortney M Howard, Mariam Hovhannisyan, Maureen Ritchey, Roberto Cabeza, Simon W Davi. Hippocampal functions modulate transfer-appropriate cortical representations supporting subsequent memory. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2023-12-05. PMID:38050089. critically, hippocampal functions modulated the mnemonic impact of cortical representations that are most pertinent to future memory demands, or 2023-12-05 2023-12-10 human
Ofer Perl, Or Duek, Kaustubh R Kulkarni, Charles Gordon, John H Krystal, Ifat Levy, Ilan Harpaz-Rotem, Daniela Schille. Neural patterns differentiate traumatic from sad autobiographical memories in PTSD. Nature neuroscience. vol 26. issue 12. 2023-11-30. PMID:38036701. an intersubject representational similarity analysis of cross-subject semantic content and neural patterns revealed a differentiation in hippocampal representation by narrative type: semantically similar, sad autobiographical memories elicited similar neural representations across participants. 2023-11-30 2023-12-10 human
Jiajun Liao, Jinhui Li, Yidan Qiu, Xiaoyan Wu, Bingyi Liu, Lu Zhang, Yuting Zhang, Xiaoqi Peng, Ruiwang Huan. Dissociable contributions of the hippocampus and orbitofrontal cortex to representing task space in a social context. Cerebral cortex (New York, N.Y. : 1991). 2023-11-27. PMID:38011099. the hippocampus (hc) and the orbitofrontal cortex (ofc) jointly encode a map-like representation of a task space to guide behavior. 2023-11-27 2023-11-29 human