Evidence map›Paper›PMID 25034823›Full record

ArticleLearning & memory (Cold Spring Harbor, N.Y.)2014

Genetic disruption of the core circadian clock impairs hippocampus-dependent memory.

Sarah M Wardlaw, Trongha X Phan, Amit Saraf, Xuanmao Chen, Daniel R Storm

Erratum issuedOpen access · diamondAbstract read
In one paragraph

Article in Learning & memory (Cold Spring Harbor, N.Y.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
–field-weighted citation impact
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

83 citing papers in PubMed, 110 citations in OpenAlex.

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  18. A high-light therapy restores the circadian clock and corrects the pathological syndrome generated in restricted-fed mice.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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23 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Sarah M WardlawDepartment of Pharmacology, School of Medicine, University of Washington, Seattle, Washington 98195-7750, USA.
Trongha X PhanDepartment of Pharmacology, School of Medicine, University of Washington, Seattle, Washington 98195-7750, USA.
Amit SarafDepartment of Pharmacology, School of Medicine, University of Washington, Seattle, Washington 98195-7750, USA.
Xuanmao ChenDepartment of Pharmacology, School of Medicine, University of Washington, Seattle, Washington 98195-7750, USA.
Daniel R StormDepartment of Pharmacology, School of Medicine, University of Washington, Seattle, Washington 98195-7750, USA dstorm@u.washington.edu.
University of Washington · US

Funding

PURIFICATION AND CHARACTERIZATION OF ADENYLATE CYCLASER01NS020498 · NINDS · UNIVERSITY OF WASHINGTON · PI STORM, DANIEL R · 1985 to 2013
$4.9M
Memory Enhancement by A Genetic Increase in cAMP SignalsR01MH073601 · NIMH · UNIVERSITY OF WASHINGTON · PI STORM, DANIEL R · 2006 to 2015
$3.5M
NIMH NIH HHS MH 073601NIMH NIH HHS R01 MH073601NINDS NIH HHS NS 20498NINDS NIH HHS R01 NS020498
6 · The paper itself

Abstract

Perturbing the circadian system by electrolytically lesioning the suprachiasmatic nucleus (SCN) or varying the environmental light:dark schedule impairs memory, suggesting that memory depends on the circadian system. We used a genetic approach to evaluate the role of the molecular clock in memory. Bmal1-/- mice, which are arrhythmic under constant conditions, were examined for hippocampus-dependent memory, LTP at the Schaffer-collateral synapse, and signal transduction activity in the hippocampus. Bmal1-/- mice exhibit impaired contextual fear and spatial memory. Furthermore, LTP in hippocampal slices from Bmal1-/- mice is also significantly decreased relative to that from wild-type mice. Activation of Erk1,2 MAP kinase (MAPK) during training for contextual fear memory and diurnal oscillation of MAPK activity and cAMP in the hippocampus is also lost in Bmal1-/- mice, suggesting that the memory defects are due to reduction of the memory consolidation pathway in the hippocampus. We conclude that critical signaling events in the hippocampus required for memory depend on BMAL1.

Indexed as

Long-Term PotentiationActigraphyAnimalsARNTL Transcription FactorsBlotting, WesternCircadian ClocksElectroshockEnzyme-Linked Immunosorbent AssayFearFootFreezing Reaction, CatalepticHippocampusMaleMAP Kinase Signaling SystemMaze LearningMemoryARNTL Transcription FactorsBmal1 protein, mouse

Identifiers

PMID25034823
PMCPMC4105720
OpenAlexW2326783248

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.