cfos principal cells and interneurons are strongly reactivated by sharp wave ripples DOI Creative Commons
Masood‐ul‐Hassan Javed, E. M. Robles-Hernandez, Rina Patel

и другие.

bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2024, Номер unknown

Опубликована: Дек. 17, 2024

Abstract The hippocampal formation is central for the learning and consolidation of spatial memories. While it known that high-frequency oscillations, called sharp wave ripples, play a critical role memory processes, unclear if they interact with engram cells. Here we identify effect these oscillations on cells as mice explored two environments over several days. We found both principal interneurons are part cfos-tagged engram. cells, place highly reactivated by SWRs, whereas none negatively SWR-modulated Together, our findings reveal link between cellular network mechanisms imply key in it.

Язык: Английский

Sleep loss diminishes hippocampal reactivation and replay DOI
Bapun Giri, Nathaniel R. Kinsky, Utku Kaya

и другие.

Nature, Год журнала: 2024, Номер 630(8018), С. 935 - 942

Опубликована: Июнь 12, 2024

Язык: Английский

Процитировано

19

Mental exploration of future choices during immobility theta oscillations DOI Open Access
Mengni Wang, Li Yuan, Stefan Leutgeb

и другие.

bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2025, Номер unknown

Опубликована: Фев. 3, 2025

SUMMARY Mental exploration enables flexible evaluation of potential future choices, guiding decision-making without requiring direct real-world iterations. Although the hippocampus is known to be active while imagining future, precise mechanisms that support mental choices remain unclear. In hippocampus, theta rhythm (4-12 Hz) prevalent during movement and supports memory coding by organizing neuronal activity patterns into short virtual path segments (theta sequences) around rat’s location. We observed these theta-related neural in a hippocampus-dependent working task also, unexpectedly, oscillations immobility. Compared standard sequences movement, immobility differed they occurred at shifted phase preferentially represented remote locations, particular next choice task. Coding for locations was also awake sharp wave ripple, but short-lasting events rarely were biased toward frequently visited locations. Therefore, our findings suggest recurring bouts immobility, which are primates humans, cognitive demands hippocampal network facilitate ongoing predictions choices.

Язык: Английский

Процитировано

1

Sleep stages antagonistically modulate reactivation drift DOI Creative Commons

Lars Bollmann,

Péter Baracskay,

Federico Stella

и другие.

Neuron, Год журнала: 2025, Номер unknown

Опубликована: Март 1, 2025

Язык: Английский

Процитировано

1

Memory engram stability and flexibility DOI Creative Commons
Yosif Zaki, Denise J. Cai

Neuropsychopharmacology, Год журнала: 2024, Номер 50(1), С. 285 - 293

Опубликована: Сен. 18, 2024

Язык: Английский

Процитировано

6

The predictive nature of spontaneous brain activity across scales and species DOI Creative Commons
Anastasia Dimakou, Giovanni Pezzulo, Andrea Zangrossi

и другие.

Neuron, Год журнала: 2025, Номер unknown

Опубликована: Март 1, 2025

Язык: Английский

Процитировано

0

Awake replay: off the clock but on the job DOI Creative Commons
Matthijs A. A. van der Meer, Daniel Bendor

Trends in Neurosciences, Год журнала: 2025, Номер unknown

Опубликована: Март 1, 2025

Hippocampal replay is widely thought to support two key cognitive functions: online decision-making and offline memory consolidation. In this review, we take a closer look at the hypothesized link between awake in rodents, find only marginal evidence of role. By contrast, consolidation view bolstered by new computational ideas recent data, suggesting that (i) performs fictive learning for later goal-oriented behavior; (ii) tags memories prior sleep, prioritizing them Based on these advances, favor an updated refined role - is, supporting prioritized tagging outside hippocampus rather than direct, guiding behavior.

Язык: Английский

Процитировано

0

Hippocampal reactivation and replay: Findings and insights from rodent studies DOI
Brian Kim, Kamran Diba

Elsevier eBooks, Год журнала: 2025, Номер unknown

Опубликована: Янв. 1, 2025

Язык: Английский

Процитировано

0

Sleep doesn’t just consolidate memories; it actively shapes them DOI
Giorgia Guglielmi

The Transmitter, Год журнала: 2025, Номер unknown

Опубликована: Янв. 1, 2025

Язык: Английский

Процитировано

0

Novel off-context experience constrains hippocampal representational drift DOI
Gal Elyasaf,

Alon Rubin,

Yaniv Ziv

и другие.

Current Biology, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 1, 2024

Язык: Английский

Процитировано

2

Single field evolution rule governs the dynamics of representational drift in mouse hippocampal dorsal CA1 region DOI Creative Commons
Cong Chen, Shuyang Yao,

Sihui Cheng

и другие.

bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2024, Номер unknown

Опубликована: Июль 29, 2024

Summary How the brain reconciles dynamism with stability to balance learning and reliable memory storage has not yet been fully understood. To address critical question, we longitudinally recorded place cells in hippocampal dorsal CA1 region over 7 56 days, utilizing multiple goal-oriented navigation paradigms across various environments. We found that 80% of displayed fields, undergoing complex evolution events including field disappearance, formation, retention. Place fields from same neuron showed limited coordination (∼5%), a preference for synchronized changes. further uncovered single rule: longer remains active, more likely it is continue being active; conversely, inactive, less recover future fate depends on its past activity. Mathematical modeling revealed this rule sufficiently demonstrates growing dCA1 spatial representation at population level.

Язык: Английский

Процитировано

1