scholarly journals Phase precession in the human hippocampus and entorhinal cortex

Cell ◽  
2021 ◽  
Author(s):  
Salman E. Qasim ◽  
Itzhak Fried ◽  
Joshua Jacobs
2020 ◽  
Author(s):  
Salman E. Qasim ◽  
Itzhak Fried ◽  
Joshua Jacobs

AbstractKnowing where we are, where we have been, and where we are going is critical to many behaviors, including navigation and memory. One potential neuronal mechanism underlying this ability is phase precession, in which spatially tuned neurons represent sequences of positions by activating at progressively earlier phases of local network theta (~5–10 Hz) oscillations. Phase precession may be a general neural pattern for representing sequential events for learning and memory. However, phase precession has never been observed in humans. By recording human single-neuron activity during spatial navigation, we show that spatially tuned neurons in the human hippocampus and entorhinal cortex exhibit phase precession. Furthermore, beyond the neural representation of locations, we show evidence for phase precession related to specific goal-states. Our findings thus extend theta phase precession to humans and suggest that this phenomenon has a broad functional role for the neural representation of both spatial and non-spatial information.


Author(s):  
Gray Umbach ◽  
Pranish Kantak ◽  
Joshua Jacobs ◽  
Michael Kahana ◽  
Brad E. Pfeiffer ◽  
...  

AbstractThe organization of temporal information is critical for the encoding and retrieval of episodic memories. In the rodent hippocampus and entorhinal cortex, recent evidence suggests that temporal information is encoded by a population of “time cells.” We identify time cells in humans using intracranial microelectrode recordings obtained from 27 human epilepsy patients who performed an episodic memory task. We show that time cell activity predicts the temporal organization of episodic memories. A significant portion of these cells exhibits phase precession, a key phenomenon not previously seen in human recordings. These findings establish a cellular mechanism for the representation of temporal information in the human brain needed to form episodic memories.


2013 ◽  
Vol 2013 ◽  
pp. 1-19 ◽  
Author(s):  
Patrick Greene ◽  
Mike Howard ◽  
Rajan Bhattacharyya ◽  
Jean-Marc Fellous

The human hippocampus receives distinct signals via the lateral entorhinal cortex, typically associated with object features, and the medial entorhinal cortex, associated with spatial or contextual information. The existence of these distinct types of information calls for some means by which they can be managed in an appropriate way, by integrating them or keeping them separate as required to improve recognition. We hypothesize that several anatomical features of the hippocampus, including differentiation in connectivity between the superior/inferior blades of DG and the distal/proximal regions of CA3 and CA1, work together to play this information managing role. We construct a set of neural network models with these features and compare their recognition performance when given noisy or partial versions of contexts and their associated objects. We found that the anterior and posterior regions of the hippocampus naturally require different ratios of object and context input for optimal performance, due to the greater number of objects versus contexts. Additionally, we found that having separate processing regions in DG significantly aided recognition in situations where object inputs were degraded. However, split processing in both DG and CA3 resulted in performance tradeoffs, though the actual hippocampus may have ways of mitigating such losses.


2016 ◽  
Vol 36 (7) ◽  
pp. 2283-2288 ◽  
Author(s):  
Eric T. Reifenstein ◽  
Christian L. Ebbesen ◽  
Qiusong Tang ◽  
Michael Brecht ◽  
Susanne Schreiber ◽  
...  

2012 ◽  
Vol 109 (16) ◽  
pp. 6301-6306 ◽  
Author(s):  
E. T. Reifenstein ◽  
R. Kempter ◽  
S. Schreiber ◽  
M. B. Stemmler ◽  
A. V. M. Herz

2020 ◽  
Vol 117 (45) ◽  
pp. 28463-28474 ◽  
Author(s):  
Gray Umbach ◽  
Pranish Kantak ◽  
Joshua Jacobs ◽  
Michael Kahana ◽  
Brad E. Pfeiffer ◽  
...  

The organization of temporal information is critical for the encoding and retrieval of episodic memories. In the rodent hippocampus and entorhinal cortex, evidence accumulated over the last decade suggests that populations of “time cells” in the hippocampus encode temporal information. We identify time cells in humans using intracranial microelectrode recordings obtained from 27 human epilepsy patients who performed an episodic memory task. We show that time cell activity predicts the temporal organization of retrieved memory items. We also uncover evidence of ramping cell activity in humans, which represents a complementary type of temporal information. These findings establish a cellular mechanism for the representation of temporal information in the human brain needed to form episodic memories.


2021 ◽  
Author(s):  
Yanbo Lian ◽  
Anthony N. Burkitt

Hippocampal place cells have spatio-temporal properties: they generally respond to a single spatial position of a small environment; in addition, they also display a temporal property, the theta phase precession, namely that the phase of spiking relative to the theta wave shifts from the late phase to early phase as the animal crosses the place field. Grid cells in layer II of medial entorhinal cortex (MEC) also have spatio-temporal properties similar to hippocampal place cells, except that grid cells respond to multiple spatial locations that form a hexagonal pattern. Other non-grid spatial cells are also abundant in the entorhinal cortex (EC). EC is the upstream that projects strongly to the hippocampus, many EC-hippocampus models have been designed to explain how the spatial property of place cells emerges. However, there is no learning model explaining how the temporal properties of hippocampal place cells emerge from the EC input. A learning model is presented here based on non-negative sparse coding in which we show that the spatial and temporal properties of hippocampal place cells can be simultaneously learnt from EC input: both MEC grid cells and other EC spatial cells contribute to the spatial properties of hippocampal place cells while MEC grid cells contribute to the temporal properties of hippocampal place cells.


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