Monosynaptic hippocampal-prefrontal projections contribute to spatial memory consolidation in mice

Standard

Monosynaptic hippocampal-prefrontal projections contribute to spatial memory consolidation in mice. / Binder, Sonja; Mölle, Matthias; Lippert, Michael; Bruder, Ralf; Aksamaz, Sonat; Ohl, Frank; Wiegert, J Simon; Marshall, Lisa.

in: J NEUROSCI, Jahrgang 39, Nr. 35, 28.08.2019, S. 6978-6991.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Binder, S, Mölle, M, Lippert, M, Bruder, R, Aksamaz, S, Ohl, F, Wiegert, JS & Marshall, L 2019, 'Monosynaptic hippocampal-prefrontal projections contribute to spatial memory consolidation in mice', J NEUROSCI, Jg. 39, Nr. 35, S. 6978-6991. https://doi.org/10.1523/JNEUROSCI.2158-18.2019

APA

Binder, S., Mölle, M., Lippert, M., Bruder, R., Aksamaz, S., Ohl, F., Wiegert, J. S., & Marshall, L. (2019). Monosynaptic hippocampal-prefrontal projections contribute to spatial memory consolidation in mice. J NEUROSCI, 39(35), 6978-6991. https://doi.org/10.1523/JNEUROSCI.2158-18.2019

Vancouver

Bibtex

@article{5a48457390b6489f8935618df01d4fe1,
title = "Monosynaptic hippocampal-prefrontal projections contribute to spatial memory consolidation in mice",
abstract = "Time locking between neocortical sleep slow oscillations, thalamo-cortical spindles, and hippocampal sharp-wave ripples has convincingly been shown to be a key element of systems consolidation. Here we investigate the role of monosynaptic projections from ventral/intermediate hippocampus to medial prefrontal cortex (mPFC) in sleep-dependent memory consolidation in male mice. Following acquisition learning in the Barnes maze, we optogenetically silenced the axonal terminals of hippocampal projections within mPFC during slow-wave sleep. This silencing during SWS selectively impaired recent but not remote memory in the absence of effects on error rate and escape latencies. Furthermore, it prevented the development of the most efficient search strategy and sleep spindle time-locking to slow oscillation. An increase in post-learning sleep sharp-wave ripple (SPWR) density and reduced time locking of learning-associated SPWR activity to sleep spindles may be a less specific response. Our results demonstrate that monosynaptic projections from hippocampus to mPFC contribute to sleep-dependent memory consolidation, potentially by affecting the temporal coupling of sleep-associated electrophysiological events.SIGNIFICANCE STATEMENT Convincing evidence supports the role of slow-wave sleep (SWS), and the relevance of close temporal coupling of neuronal activity between brain regions for systems consolidation. Less attention has been paid so far to the specific neuronal pathways underlying these processes. Here, we optogenetically silenced the direct monosynaptic projection from ventral/intermediate hippocampus (HC) to medial prefrontal cortex (mPFC) during SWS in male mice following repeated learning trials in a weakly aversive spatial task. Our results confirm the concept that the monosynaptic projection between HC and mPFC contributes to memory consolidation and support an important functional role of this pathway in shaping the temporal precision among sleep-associated electrophysiological events.",
author = "Sonja Binder and Matthias M{\"o}lle and Michael Lippert and Ralf Bruder and Sonat Aksamaz and Frank Ohl and Wiegert, {J Simon} and Lisa Marshall",
note = "Copyright {\textcopyright} 2019 the authors.",
year = "2019",
month = aug,
day = "28",
doi = "10.1523/JNEUROSCI.2158-18.2019",
language = "English",
volume = "39",
pages = "6978--6991",
journal = "J NEUROSCI",
issn = "0270-6474",
publisher = "Society for Neuroscience",
number = "35",

}

RIS

TY - JOUR

T1 - Monosynaptic hippocampal-prefrontal projections contribute to spatial memory consolidation in mice

AU - Binder, Sonja

AU - Mölle, Matthias

AU - Lippert, Michael

AU - Bruder, Ralf

AU - Aksamaz, Sonat

AU - Ohl, Frank

AU - Wiegert, J Simon

AU - Marshall, Lisa

N1 - Copyright © 2019 the authors.

PY - 2019/8/28

Y1 - 2019/8/28

N2 - Time locking between neocortical sleep slow oscillations, thalamo-cortical spindles, and hippocampal sharp-wave ripples has convincingly been shown to be a key element of systems consolidation. Here we investigate the role of monosynaptic projections from ventral/intermediate hippocampus to medial prefrontal cortex (mPFC) in sleep-dependent memory consolidation in male mice. Following acquisition learning in the Barnes maze, we optogenetically silenced the axonal terminals of hippocampal projections within mPFC during slow-wave sleep. This silencing during SWS selectively impaired recent but not remote memory in the absence of effects on error rate and escape latencies. Furthermore, it prevented the development of the most efficient search strategy and sleep spindle time-locking to slow oscillation. An increase in post-learning sleep sharp-wave ripple (SPWR) density and reduced time locking of learning-associated SPWR activity to sleep spindles may be a less specific response. Our results demonstrate that monosynaptic projections from hippocampus to mPFC contribute to sleep-dependent memory consolidation, potentially by affecting the temporal coupling of sleep-associated electrophysiological events.SIGNIFICANCE STATEMENT Convincing evidence supports the role of slow-wave sleep (SWS), and the relevance of close temporal coupling of neuronal activity between brain regions for systems consolidation. Less attention has been paid so far to the specific neuronal pathways underlying these processes. Here, we optogenetically silenced the direct monosynaptic projection from ventral/intermediate hippocampus (HC) to medial prefrontal cortex (mPFC) during SWS in male mice following repeated learning trials in a weakly aversive spatial task. Our results confirm the concept that the monosynaptic projection between HC and mPFC contributes to memory consolidation and support an important functional role of this pathway in shaping the temporal precision among sleep-associated electrophysiological events.

AB - Time locking between neocortical sleep slow oscillations, thalamo-cortical spindles, and hippocampal sharp-wave ripples has convincingly been shown to be a key element of systems consolidation. Here we investigate the role of monosynaptic projections from ventral/intermediate hippocampus to medial prefrontal cortex (mPFC) in sleep-dependent memory consolidation in male mice. Following acquisition learning in the Barnes maze, we optogenetically silenced the axonal terminals of hippocampal projections within mPFC during slow-wave sleep. This silencing during SWS selectively impaired recent but not remote memory in the absence of effects on error rate and escape latencies. Furthermore, it prevented the development of the most efficient search strategy and sleep spindle time-locking to slow oscillation. An increase in post-learning sleep sharp-wave ripple (SPWR) density and reduced time locking of learning-associated SPWR activity to sleep spindles may be a less specific response. Our results demonstrate that monosynaptic projections from hippocampus to mPFC contribute to sleep-dependent memory consolidation, potentially by affecting the temporal coupling of sleep-associated electrophysiological events.SIGNIFICANCE STATEMENT Convincing evidence supports the role of slow-wave sleep (SWS), and the relevance of close temporal coupling of neuronal activity between brain regions for systems consolidation. Less attention has been paid so far to the specific neuronal pathways underlying these processes. Here, we optogenetically silenced the direct monosynaptic projection from ventral/intermediate hippocampus (HC) to medial prefrontal cortex (mPFC) during SWS in male mice following repeated learning trials in a weakly aversive spatial task. Our results confirm the concept that the monosynaptic projection between HC and mPFC contributes to memory consolidation and support an important functional role of this pathway in shaping the temporal precision among sleep-associated electrophysiological events.

U2 - 10.1523/JNEUROSCI.2158-18.2019

DO - 10.1523/JNEUROSCI.2158-18.2019

M3 - SCORING: Journal article

C2 - 31285301

VL - 39

SP - 6978

EP - 6991

JO - J NEUROSCI

JF - J NEUROSCI

SN - 0270-6474

IS - 35

ER -