Evidence map›Paper›PMID 27531979›Full record

ArticleFrontiers in aging neuroscience2016

Recurrent Sleep Fragmentation Induces Insulin and Neuroprotective Mechanisms in Middle-Aged Flies.

Michael J Williams, Emelie Perland, Mikaela M Eriksson, Josef Carlsson, Daniel Erlandsson, Loora Laan, Tabusi Mahebali, Ella Potter, Robert Frediksson, Christian Benedict and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Frontiers in cell and developmental biology · 2020
    Article
  10. Tired and stressed: Examining the need for sleep.The European journal of neuroscience · 2020
    Review
  11. Aging and the clock: Perspective from flies to humans.The European journal of neuroscience · 2020
    Review
  12. Article
  13. Article
  14. Article
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

11 authors at 1 institution in 1 country.

Michael J WilliamsFunctional Pharmacology, Department of Neuroscience, Uppsala University Uppsala, Sweden.
Emelie PerlandFunctional Pharmacology, Department of Neuroscience, Uppsala University Uppsala, Sweden.
Mikaela M ErikssonFunctional Pharmacology, Department of Neuroscience, Uppsala University Uppsala, Sweden.
Josef CarlssonFunctional Pharmacology, Department of Neuroscience, Uppsala University Uppsala, Sweden.
Daniel ErlandssonFunctional Pharmacology, Department of Neuroscience, Uppsala University Uppsala, Sweden.
Loora LaanFunctional Pharmacology, Department of Neuroscience, Uppsala University Uppsala, Sweden.
Tabusi MahebaliFunctional Pharmacology, Department of Neuroscience, Uppsala University Uppsala, Sweden.
Ella PotterFunctional Pharmacology, Department of Neuroscience, Uppsala University Uppsala, Sweden.
Robert FredikssonFunctional Pharmacology, Department of Neuroscience, Uppsala University Uppsala, Sweden.
Christian BenedictFunctional Pharmacology, Department of Neuroscience, Uppsala University Uppsala, Sweden.
Helgi B SchiöthFunctional Pharmacology, Department of Neuroscience, Uppsala University Uppsala, Sweden.
Uppsala University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lack of quality sleep increases central nervous system oxidative stress and impairs removal of neurotoxic soluble metabolites from brain parenchyma. During aging poor sleep quality, caused by sleep fragmentation, increases central nervous system cellular stress. Currently, it is not known how organisms offset age-related cytotoxic metabolite increases in order to safeguard neuronal survival. Furthermore, it is not understood how age and sleep fragmentation interact to affect oxidative stress protection pathways. We demonstrate sleep fragmentation increases systems that protect against oxidative damage and neuroprotective endoplasmic reticulum molecular chaperones, as well as neuronal insulin and dopaminergic expression in middle-aged Drosophila males. Interestingly, even after sleep recovery the expression of these genes was still upregulated in middle-aged flies. Finally, sleep fragmentation generates higher levels of reactive oxygen species (ROS) in middle-aged flies and after sleep recovery these levels remain significantly higher than in young flies. The fact that neuroprotective pathways remain upregulated in middle-aged flies beyond sleep fragmentation suggests it might represent a strong stressor for the brain during later life.

Indexed as

dopamineglucagoninsulinmetabolismmolecular chaperoneNrf2sleep

Identifiers

PMID27531979
PMCPMC4969361
OpenAlexW2482457296

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.