Evidence map›Paper›PMID 36510822›Full record

ArticleSleep2023

Atypical hypnotic compound ML297 restores sleep architecture immediately following emotionally valenced learning, to promote memory consolidation and hippocampal network activation during recall.

Jessy D Martinez, William P Brancaleone, Kathryn G Peterson, Lydia G Wilson, Sara J Aton

Open access · hybridAbstract read
In one paragraph

Article in Sleep, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 12 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Jessy D MartinezDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48109, USA.ORCID 0000-0001-9811-7626
William P BrancaleoneUndergraduate Program in Neuroscience, University of Michigan, Ann Arbor, MI 48109, USA.ORCID 0000-0002-4644-1544
Kathryn G PetersonUndergraduate Program in Neuroscience, University of Michigan, Ann Arbor, MI 48109, USA.
Lydia G WilsonDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48109, USA.
Sara J AtonDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48109, USA.ORCID 0000-0002-2921-0509
University of Michigan · US

Funding

Thalamocortical and corticocortical mechanisms for sleep-dependent visual learningR01NS104776 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ATON, SARA J · 2018 to 2022
$1.9M
Linking interneuron-mediated circuit regulation with sleep-dependent plasticity and memory storage in the hippocampusRF1NS118440 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ATON, SARA J · 2020 to 2020
$1.4M
Linking interneuron-mediated circuit regulation with sleep-dependent plasticity and memory storage in the hippocampusR01NS118440 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ATON, SARA J · 2023 to 2024
$880k
NIH HHS R01 NS104776NINDS NIH HHS R01 NS118440NINDS NIH HHS RF1 NS118440
6 · The paper itself

Abstract

Sleep plays a critical role in consolidating many forms of hippocampus-dependent memory. While various classes of hypnotic drugs have been developed in recent years, it remains unknown whether, or how, some of them affect sleep-dependent memory consolidation mechanisms. We find that ML297, a recently developed candidate hypnotic agent targeting a new mechanism (activating GIRK1/2-subunit containing G-protein coupled inwardly rectifying potassium [GIRK] channels), alters sleep architecture in mice over the first 6 hr following a single-trial learning event. Following contextual fear conditioning (CFC), ML297 reversed post-CFC reductions in NREM sleep spindle power and REM sleep amounts and architecture, renormalizing sleep features to what was observed at baseline, prior to CFC. Renormalization of post-CFC REM sleep latency, REM sleep amounts, and NREM spindle power were all associated with improved contextual fear memory (CFM) consolidation. We find that improvements in CFM consolidation due to ML297 are sleep-dependent, and are associated with increased numbers of highly activated dentate gyrus (DG), CA1, and CA3 neurons during CFM recall. Together our findings suggest that GIRK1/2 channel activation restores normal sleep architecture- including REM sleep, which is normally suppressed following CFC-and increases the number of hippocampal neurons incorporated into the CFM engram during memory consolidation.

Indexed as

Memory ConsolidationAnimalsHippocampusHypnotics and SedativesLearningMiceSleepHypnotics and Sedativeshippocampushypnotic drugmemory consolidationREMspindles

Identifiers

PMID36510822
PMCPMC9995787
OpenAlexW4311282554

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.