Cited by 131Memory and Neural MechanismsNeurogenesis and neuroplasticity mechanismsSleep and Wakefulness Research

Emergence of preconfigured and plastic time-compressed sequences in early postnatal development

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Farooq, U., Dragoi, G.·2019·Science

Abstract

Memory capabilities develop with age: During memory formation, time-compressed neuronal sequences underlie consolidation as well as encoding of novel information. Such memory traces are largely contributed by a selection of preconfigured neuronal patterns. However, when and how these preconfigured patterns first emerge in the hippocampus is unknown. Farooq and Dragoi identified an age-dependent development of network preconfiguration into trajectory-like sequences. This preconfiguration was expressed spontaneously during sleep and emerged from the assembly of persistent, location-depicting ensembles, largely controlled by intrinsic developmental programs. Thus, the compressed binding of adjacent locations into spatial trajectories during navigation and their experience-dependent replay emerge in coordination from spontaneous preconfigured sequences. Science , this issue p. 168

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  • In the rodent hippocampus, at the end of the first postnatal week, sharp wave bursts can be detected, while SPW-Rs in conjunction with neuronal reactivations only emerge at the end of the second postnatal week.

    “In the rodent hippocampus, at the end of the first postnatal week, ''sharp wave bursts,'' as a first organized network event can be detected, while SPW-Rs in conjunction with neuronal reactivations only emerge at the end of the second postnatal week.255,256”

    From Sleep—A brain-state serving systems memory consolidation (2023) · cites this paper as [256]

    The paper’s account of awake rest and sleep reports location-depicting neuronal activity at P15–P16, and says spatial experience–depicting frames co-occurred with ripple oscillations (Fig. 3–4 passages; page unavailable). Its recordings began at P15, however, so it does not establish when sharp-wave bursts first appear in postnatal week one or that SPW-Rs with neuronal reactivation first emerge at the end of week two. (LLM, conf=0.76)

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Research works printed but not linked: 2

  1. [13]O’Keefe J, Nadel L, The Hippocampus as a Cognitive Map. (Oxford University Press, Oxford, 1978).
  2. [29]Kant I, Critique of Pure Reason. (Cambridge University Press, Cambridge, UK, 1781).

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Authors
Farooq, U., & Dragoi, G.
Affiliations
Yale University (US)
Corresponding author
Dragoi, G.
Venue
Science
Published
2019-01-11
Volume
363
Issue
6423
Pages
168-173
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2908664654
Cited by
131
References
31
Citations by year
2026: 10 · 2025: 16 · 2024: 22 · 2023: 23 · 2022: 15 · 2021: 27 · 2020: 11 · 2019: 7
FWCI
8.72
Type
journal article
Language
en
Open access
Locations
  • Science (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • Brain and Behavior Research Foundation
  • Whitehall Foundation
  • Charles H. Hood Foundation
  • Gruber Foundation
  • NINDS
Topics
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
  • Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
Keywords
postnatal development, hippocampal replay, sleep, memory consolidation, episodic memory, spatial navigation
MeSH terms
Age Factors, Animals, Animals, Newborn, Male, Neurons, Sleep, Theta Rhythm, Rats, Long-Evans, Rats, Electrophysiological Phenomena, CA1 Region, Hippocampal, Memory, Episodic, Spatial Memory

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