Evidence map›Paper›PMID 25142573›Full record

ArticleSleep2014

Genetic rescue of functional senescence in synaptic and behavioral plasticity.

Jeffrey M Donlea, Narendrakumar Ramanan, Neal Silverman, Paul J Shaw

Open access · bronzeAbstract read
In one paragraph

Article in Sleep, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

17 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Activity Monitoring for Analysis of Sleep inCold Spring Harbor protocols · 2024
    Article
  3. Article
  4. Article
  5. Article
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  10. Aging and the clock: Perspective from flies to humans.The European journal of neuroscience · 2020
    Review
  11. Article
  12. Article
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  14. Article
  15. Article
  16. Acetylcholine from Visual Circuits Modulates the Activity of Arousal Neurons in Drosophila.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  17. Sleep, Performance, and Memory in Flies.Current sleep medicine reports · 2015
    Review
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

4 authors at 2 institutions in 1 country.

Jeffrey M Donlea
Narendrakumar Ramanan
Neal Silverman
Paul J Shaw
Washington University in St. Louis · USUniversity of Massachusetts Chan Medical School · US

Funding

Washington University Center for Translational NeuroscienceP30NS057105 · NINDS · WASHINGTON UNIVERSITY · PI HOLTZMAN, DAVID M. · 2006 to 2011
$8.7M
GENETIC ANALYSIS OF SLEEP SENECENCEP01AG033561 · NIA · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI BODMER, ROLF · 2011 to 2015
$6.3M
FUNCTIONAL ANALYSIS OF SLEEP HOMEOSTASIS IN DROSOPHILAR01NS051305 · NINDS · WASHINGTON UNIVERSITY · PI SHAW, PAUL J · 2005 to 2023
$6.1M
Role of Drosophila circadian circuitry in experience-dependent sleepF31NS063514 · NINDS · WASHINGTON UNIVERSITY · PI DONLEA, JEFFREY MICHAEL · 2009 to 2010
$39k
NIA NIH HHS 1 P01AG033561-01NIA NIH HHS P01 AG033561NINDS NIH HHS F31 NS063514NINDS NIH HHS P30 NS057105NINDS NIH HHS R01 NS051305
6 · The paper itself

Abstract

STUDY

objectivesAging has been linked with decreased neural plasticity and memory formation in humans and in laboratory model species such as the fruit fly, Drosophila melanogaster. Here, we examine plastic responses following social experience in Drosophila as a high-throughput method to identify interventions that prevent these impairments. PATIENTS OR

participantsWild-type and transgenic Drosophila melanogaster. DESIGN AND

interventionsYoung (5-day old) or aged (20-day old) adult female Drosophila were housed in socially enriched (n = 35-40) or isolated environments, then assayed for changes in sleep and for structural markers of synaptic terminal growth in the ventral lateral neurons (LNVs) of the circadian clock. MEASUREMENTS AND

resultsWhen young flies are housed in a socially enriched environment, they exhibit synaptic elaboration within a component of the circadian circuitry, the LNVs, which is followed by increased sleep. Aged flies, however, no longer exhibit either of these plastic changes. Because of the tight correlation between neural plasticity and ensuing increases in sleep, we use sleep after enrichment as a high-throughput marker for neural plasticity to identify interventions that prolong youthful plasticity in aged flies. To validate this strategy, we find three independent genetic manipulations that delay age-related losses in plasticity: (1) elevation of dopaminergic signaling, (2) over-expression of the transcription factor blistered (bs) in the LNVs, and (3) reduction of the Imd immune signaling pathway. These findings provide proof-of-principle evidence that measuring changes in sleep in flies after social enrichment may provide a highly scalable assay for the study of age-related deficits in synaptic plasticity.

conclusionsThese studies demonstrate that Drosophila provides a promising model for the study of age-related loss of neural plasticity and begin to identify genes that might be manipulated to delay the onset of functional senescence.

Indexed as

Social BehaviorAgingAnimalsAnimals, Genetically ModifiedBiological AssayBiomarkersCarrier ProteinsCircadian RhythmDopaminergic NeuronsDrosophila melanogasterDrosophila ProteinsFemaleHigh-Throughput Screening AssaysImmunityMaleMemoryBiomarkersCarrier ProteinsDrosophila Proteinspeptidoglycan recognition proteinagingDrosophilaplasticity

Identifiers

PMID25142573
PMCPMC4153059
OpenAlexW2028777734

What OpenQuestion holds

Textmetadata
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.