Evidence map›Paper›PMID 24102714›Full record

ArticleAging cell2014

Aging and sleep deprivation induce the unfolded protein response in the pancreas: implications for metabolism.

Nirinjini Naidoo, James G Davis, Jingxu Zhu, Maya Yabumoto, Kristan Singletary, Marishka Brown, Raymond Galante, Beamon Agarwal, Joseph A Baur

Open access · hybridAbstract read
In one paragraph

Article in Aging cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

28 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. The impact of insomnia on frailty and the hallmarks of aging.Aging clinical and experimental research · 2023
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Exploring phylogeny to find the function of sleep.Nature reviews. Neuroscience · 2019
    Review
  19. The neurobiological basis of sleep: Insights from Drosophila.Neuroscience and biobehavioral reviews · 2018
    Review
  20. The potential use of physical resilience to predict healthy aging.Pathobiology of aging & age related diseases · 2018
    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

9 authors at 1 institution in 1 country.

Nirinjini NaidooDivision of Sleep Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA; Center for Sleep and Circadian Neurobiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
James G Davis
Jingxu Zhu
Maya Yabumoto
Kristan Singletary
Marishka Brown
Raymond Galante
Beamon Agarwal
Joseph A Baur
University of Pennsylvania · US

Funding

VIRAL VECTOR COREP30DK019525 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI Patrick Seale · 1986 to 2026
$48.3M
THE ROLE OF SLEEP IN MEMORY STORAGEP01AG017628 · NIA · UNIVERSITY OF PENNSYLVANIA · PI PACK, ALLAN I · 2001 to 2017
$19.2M
Age Impaired ER Homeostasis in Wake-Active Neurons: BiP/Nox2 CrosstalkR21AG032500 · NIA · UNIVERSITY OF PENNSYLVANIA · PI NAIDOO, NIRMALA NIRINJINI · 2008 to 2009
$557k
NIA NIH HHS AG23500NIA NIH HHS P01 AG017628NIA NIH HHS R21 AG032500NIDDK NIH HHS DK 19525NIDDK NIH HHS P30 DK019525
6 · The paper itself

Abstract

Sleep disruption has detrimental effects on glucose metabolism through pathways that remain poorly defined. Although numerous studies have examined the consequences of sleep deprivation (SD) in the brain, few have directly tested its effects on peripheral organs. We examined several tissues in mice for induction of the unfolded protein response (UPR) following acute SD. In young animals, we found a robust induction of BiP in the pancreas, indicating an active UPR. At baseline, pancreata from aged animals exhibited a marked increase in a pro-apoptotic transcription factor, CHOP, that was amplified by SD, whereas BiP induction was not observed, suggesting a maladaptive response to cellular stress with age. Acute SD increased plasma glucose levels in both young and old animals. However, this change was not overtly related to stress in the pancreatic beta cells, as plasma insulin levels were not lower following acute SD. Accordingly, animals subjected to acute SD remained tolerant to a glucose challenge. In a chronic SD experiment, young mice were found to be sensitized to insulin and have improved glycemic control, whereas aged animals became hyperglycemic and failed to maintain appropriate plasma insulin concentrations. Our results show that both age and SD cooperate to induce the UPR in pancreatic tissue. While changes in insulin secretion are unlikely to play a major role in the acute effects of SD, CHOP induction in pancreatic tissues suggests that chronic SD may contribute to the loss or dysfunction of endocrine cells and that these effects may be exacerbated by normal aging.

Indexed as

Unfolded Protein ResponseAgingAnimalsBlood GlucoseCentral Nervous SystemCorticosteroneFoodGlucose Tolerance TestHomeostasisInsulinMaleMiceMice, Inbred C57BLPancreasSleep DeprivationBlood GlucoseCorticosteroneInsulinagingbehaviorglucose tolerancemousesleep deprivation

Identifiers

PMID24102714
PMCPMC4009977
OpenAlexW2015147584

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.