Evidence map›Paper›PMID 29579685›Full record

ArticleNeurobiology of aging2018

Impact of insulin signaling and proteasomal activity on physiological output of a neuronal circuit in aging Drosophila melanogaster.

Hrvoje Augustin, Kieran McGourty, Marcus J Allen, Jennifer Adcott, Chi Tung Wong, Emmanuel Boucrot, Linda Partridge

Open access · hybridAbstract read
In one paragraph

Article in Neurobiology of aging, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 29% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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  4. Cell type-specific modulation of healthspan by Forkhead family transcription factors in the nervous system.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
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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

7 authors at 4 institutions in 3 countries.

Hrvoje AugustinMax Planck Institute for Biology of Ageing, Köln, Germany; Institute of Healthy Ageing, and GEE, University College London, London, UK.
Kieran McGourtyDepartment of Structural and Molecular Biology, London, UK; The Bernal Institute, University of Limerick, Limerick, Ireland.
Marcus J AllenSchool of Biosciences, University of Kent, Canterbury, Kent, UK.
Jennifer AdcottInstitute of Healthy Ageing, and GEE, University College London, London, UK.
Chi Tung WongInstitute of Healthy Ageing, and GEE, University College London, London, UK.
Emmanuel BoucrotDepartment of Structural and Molecular Biology, London, UK.
Linda PartridgeMax Planck Institute for Biology of Ageing, Köln, Germany; Institute of Healthy Ageing, and GEE, University College London, London, UK. Electronic address: partridge@age.mpg.de.
MRC Unit for Lifelong Health and Ageing · GBInstitute of Structural and Molecular Biology · GBUniversity of Kent · GBUniversity of Limerick · IE

Funding

Wellcome TrustWellcome Trust WT098565
6 · The paper itself

Abstract

The insulin family of growth factors plays an important role in development and function of the nervous system. Reduced insulin and insulin-growth-factor signaling (IIS), however, can improve symptoms of neurodegenerative diseases in laboratory model organisms and protect against age-associated decline in neuronal function. Recently, we showed that chronic, moderately lowered IIS rescues age-related decline in neurotransmission through the Drosophila giant fiber escape response circuit. Here, we expand our initial findings by demonstrating that reduced functional output in the giant fiber system of aging flies can be prevented by increasing proteasomal activity within the circuit. Manipulations of IIS in neurons can also affect longevity, underscoring the relevance of the nervous system for aging.

Indexed as

AgingAnimalsCells, CulturedDrosophila melanogasterDrosophila ProteinsGTP PhosphohydrolasesInsulinIntercellular Signaling Peptides and ProteinsLongevityNeuronsProteasome Endopeptidase Complexrab11 GTP-Binding Proteinsrab GTP-Binding ProteinsSignal TransductionSomatomedinsSynaptic TransmissionDrosophila ProteinsGTP PhosphohydrolasesInsulinIntercellular Signaling Peptides and ProteinsProteasome Endopeptidase Complexrab11 GTP-Binding ProteinsRab11 protein, DrosophilaRab4 protein, Drosophilarab GTP-Binding ProteinsSomatomedinsAgingDrosophilaGao junctionsGiant Fiber systemInsulin signalingProteasomal activityRab11Rab4Recycling

Identifiers

PMID29579685
PMCPMC5933513
OpenAlexW2789256141

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.