785 research outputs found

    Conjunctive representations in the hippocampus: What and where?

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    The context in which events occur can be represented as both (1) a set of independent features, the feature representation view, and (2) a set of features bound into a unitary representation, the conjunction representation view. It is assumed that extrahippocampal (e.g., neocortical) areas provide a basis for feature representations, but the hippocampal formation makes an essential contribution to the automatic storage of conjunctive representations. We develop this dual-representation view and explore its implications for hippocampal contributions to contextual fear conditioning processes. To this end, we discuss how our framework can resolve some of the conflicts in the recent literature relating the hippocampus to contextual fear conditioning. We also present new data supporting the role of a key mechanism afforded by conjunctive representations--pattern completion (the ability of a subset of a memory pattern to activate the complete memory)--in contextual fear conditioning. As is implied by this mechanism, we report that fear can be conditioned to the memory representation of a context that is not actually present at the time of shock. Moreover, this result is predicted by our computational model of cortical and hippocampal function. We suggest that pattern completion demonstrated in animals and by our model provides a mechanistic bridge to human declarative memory

    Establishing the boundaries: the hippocampal contribution to imagining scenes

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    When we visualize scenes, either from our own past or invented, we impose a viewpoint for our “mind's eye” and we experience the resulting image as spatially coherent from that viewpoint. The hippocampus has been implicated in this process, but its precise contribution is unknown. We tested a specific hypothesis based on the spatial firing properties of neurons in the hippocampal formation of rats, that this region supports the construction of spatially coherent mental images by representing the locations of the environmental boundaries surrounding our viewpoint. Using functional magnetic resonance imaging, we show that hippocampal activation increases parametrically with the number of enclosing boundaries in the imagined scene. In contrast, hippocampal activity is not modulated by a nonspatial manipulation of scene complexity nor to increasing difficulty of imagining the scenes in general. Our findings identify a specific computational role for the hippocampus in mental imagery and episodic recollection

    Anterior Hippocampus and Goal-Directed Spatial Decision Making

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    Contains fulltext : 115487.pdf (publisher's version ) (Open Access

    Adaptive cognitive maps for curved surfaces in a 3D world

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    Mapping sequence structure in the human lateral entorhinal cortex

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    Remembering event sequences is central to episodic memory and presumablysupported by the hippocampal-entorhinal region. We previously demonstrated that thehippocampus maps spatial and temporal distances between events encountered along a routethrough a virtual city (Deuker et al., 2016), but the content of entorhinal mnemonic representationsremains unclear. Here, we demonstrate that multi-voxel representations in the anterior-lateralentorhinal cortex (alEC) — the human homologue of the rodent lateral entorhinal cortex —specifically reflect the temporal event structure after learning. Holistic representations of thesequence structure related to memory recall and the timeline of events could be reconstructedfrom entorhinal multi-voxel patterns. Our findings demonstrate representations of temporalstructure in the alEC; dovetailing with temporal information carried by population signals in thelateral entorhinal cortex of navigating rodents and alEC activations during temporal memoryretrieval. Our results provide novel evidence for the role of the alEC in representing time forepisodic memory

    Sleep strengthens integration of spatial memory systems

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    Spatial memory comprises different representational systems that are sensitive to different environmental cues, like proximal landmarks or local boundaries. Here we examined how sleep affects the formation of a spatial representation integrating landmark-referenced and boundary-referenced representations. To this end, participants (n = 42) were familiarized with an environment featuring both a proximal landmark and a local boundary. After nocturnal periods of sleep or wakefulness and another night of sleep, integration of the two representational systems was tested by testing the participant's flexibility to switch from landmark-based to boundary-based navigation in the environment, and vice versa. Results indicate a distinctly increased flexibility in relying on either landmarks or boundaries for navigation, when familiarization to the environment was followed by sleep rather than by wakefulness. A second control study (n = 45) did not reveal effects of sleep (vs. wakefulness) on navigation in environments featuring only landmarks or only boundaries. Thus, rather than strengthening isolated representational systems per se, sleep presumably through forming an integrative representation, enhances flexible coordination of representational subsystems

    Structuring time in human lateral entorhinal cortex

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    Episodic memories consist of event information linked to spatio-temporal context. Notably, the hippocampus is involved in the encoding, representation and retrieval of temporal relations that comprise a context, but it remains largely unclear how coding for elapsed time arises in the hippocampal-entorhinal region. The entorhinal cortex (EC), the main cortical input structure of the hippocampus, has been hypothesized to provide temporal tags for memories via contextual drift and recent evidence demonstrates that time can be decoded from population activity in the rodent lateral EC. Here, we use fMRI to show that the anterior-lateral EC (alEC), the human homologue region of rodent lateral EC, maps the temporal structure of events. Participants acquired knowledge about temporal and spatial relationships between object positions - dissociated via teleporters - along a fixed route through a virtual city. Multi-voxel pattern similarity in alEC changed through learning to reflect elapsed time between event memories. Furthermore, we reconstructed the temporal structure of object relationships from alEC pattern similarity change. In contrast to the hippocampus, which maps the subjective time between event memories in this task, the temporal map in alEC reflected the objective time elapsed between events. Our findings provide evidence for the notion that alEC represents the temporal structure of memories, putatively derived from slowly-varying population signals during learning. Further, our findings suggest a dissociation between objective and subjective temporal maps in EC and hippocampus; thereby providing novel evidence for the role of the hippocampal-entorhinal region in representing time for episodic memory

    Motor affordance and its role for visual working memory: evidence from fMRI studies

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    We examined the role of motor affordances of objects for working memory retention processes. Three experiments are reported in which participants passively viewed pictures of real world objects or had to retain the objects in working memory for a comparison with an S2 stimulus. Brain activation was recorded by means of functional magnetic resonance imaging (fMRI). Retaining information about objects for which hand actions could easily be retrieved (manipulable objects) in working memory activated the hand region of the ventral premotor cortex (PMC) contralateral to the dominant hand. Conversely, nonmanipulable objects activated the left inferior frontal gyrus. This suggests that working memory for objects with motor affordance is based on motor programs associated with their use. An additional study revealed that motor program activation can be modulated by task demands: Holding manipulable objects in working memory for an upcoming motor comparison task was associated with left ventral PMC activation. However, retaining the same objects for a subsequent size comparison task led to activation in posterior brain regions. This suggests that the activation of hand motor programs are under top down control. By this they can flexibly be adapted to various task demands. It is argued that hand motor programs may serve a similar working memory function as speech motor programs for verbalizable working memory contents, and that the premotor system mediates the temporal integration of motor representations with other task-relevant representations in support of goal oriented behavior

    Mnemonic construction and representation of temporal structure in the hippocampal formation

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    The hippocampal-entorhinal region supports memory for episodic details, such as temporal relations of sequential events, and mnemonic constructions combining experiences for inferential reasoning. However, it is unclear whether hippocampal event memories reflect temporal relations derived from mnemonic constructions, event order, or elapsing time, and whether these sequence representations generalize temporal relations across similar sequences. Here, participants mnemonically constructed times of events from multiple sequences using infrequent cues and their experience of passing time. After learning, event representations in the anterior hippocampus reflected temporal relations based on constructed times. Temporal relations were generalized across sequences, revealing distinct representational formats for events from the same or different sequences. Structural knowledge about time patterns, abstracted from different sequences, biased the construction of specific event times. These findings demonstrate that mnemonic construction and the generalization of relational knowledge combine in the hippocampus, consistent with the simulation of scenarios from episodic details and structural knowledge
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