Evidence map›Paper›PMID 23699506›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2013

A dietary regimen of caloric restriction or pharmacological activation of SIRT1 to delay the onset of neurodegeneration.

Johannes Gräff, Martin Kahn, Alireza Samiei, Jun Gao, Kristie T Ota, Damien Rei, Li-Huei Tsai

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing 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

71 citing papers in PubMed.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. The roles of sirtuins in ferroptosis.Frontiers in physiology · 2023
    Review
  11. Review
  12. Review
  13. Dietary regulation in health and disease.Signal transduction and targeted therapy · 2022
    Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article

11 more citing papers are in PubMed but not listed here.

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.

Johannes GräffPicower Institute for Learning and Memory, Department of Brain and Cognitive Sciences and Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Martin Kahn
Alireza Samiei
Jun Gao
Kristie T Ota
Damien Rei
Li-Huei Tsai

Funding

THE ROLE OF Cdk5 IN THE DNA DAMAGE RESPONCE DURING AGING AND NEURODEGENERATIONP01AG027916 · NIA · HARVARD MEDICAL SCHOOL · PI YANKNER, BRUCE A · 2006 to 2010
$7.7M
Howard Hughes Medical InstituteNIA NIH HHS P01 AG027916NIA NIH HHS P01AG027916
6 · The paper itself

Abstract

Caloric restriction (CR) is a dietary regimen known to promote lifespan by slowing down the occurrence of age-dependent diseases. The greatest risk factor for neurodegeneration in the brain is age, from which follows that CR might also attenuate the progressive loss of neurons that is often associated with impaired cognitive capacities. In this study, we used a transgenic mouse model that allows for a temporally and spatially controlled onset of neurodegeneration to test the potentially beneficial effects of CR. We found that in this model, CR significantly delayed the onset of neurodegeneration and synaptic loss and dysfunction, and thereby preserved cognitive capacities. Mechanistically, CR induced the expression of the known lifespan-regulating protein SIRT1, prompting us to test whether a pharmacological activation of SIRT1 might recapitulate CR. We found that oral administration of a SIRT1-activating compound essentially replicated the beneficial effects of CR. Thus, SIRT1-activating compounds might provide a pharmacological alternative to the regimen of CR against neurodegeneration and its associated ailments.

Indexed as

Caloric RestrictionCognition DisordersNeurodegenerative DiseasesSirtuin 1Analysis of VarianceAnimalsAtrophyBrainCase-Control StudiesCyclin-Dependent Kinase 5Disease Models, AnimalExcitatory Postsynaptic PotentialsFemaleGreen Fluorescent ProteinsImmunoprecipitationIn Vitro TechniquesCdk5r1 protein, mouseCyclin-Dependent Kinase 5Green Fluorescent ProteinsNerve Tissue ProteinsPhosphopyruvate HydratasePhosphotransferasesPiperidinesSirt1 protein, mouseSirtuin 1tert-butyl 4-((2-(2-(6-(2-(tert-butoxycarbonyl(methyl)amino)ethylamino)-2-butylpyrimidine-4-carboxamido)phenyl)thiazolo(5,4-b)pyridin-6-yl)methoxy)piperidine-1-carboxylateThiazolesTumor Suppressor Protein p53Vitamin E

Identifiers

PMID23699506
PMCPMC3775567

What OpenQuestion holds

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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.