Evidence map›Paper›PMID 24412233›Full record

ArticleNeuroscience2014

Decrease in age-related tau hyperphosphorylation and cognitive improvement following vitamin D supplementation are associated with modulation of brain energy metabolism and redox state.

T L Briones, H Darwish

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

13 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Vitamin D in Neurological Diseases: A Rationale for a Pathogenic Impact.International journal of molecular sciences · 2018
    Review
  9. Vitamin DInflammopharmacology · 2018
    Article
  10. Article
  11. Review
  12. Article
  13. Vitamin D and Alzheimer's Disease: Neurocognition to Therapeutics.International journal of Alzheimer's disease · 2015
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 2 countries.

T L BrionesDepartment of Adult Health, Wayne State University, Detroit, MI 48202, United States. Electronic address: tbriones@wayne.edu.
H DarwishHariri School of Nursing, American University of Beirut, Lebanon.
American University of Beirut · LBWayne State University · US

Funding

GENE EXPRESSION-ENVIRONMENT LINK IN CEREBRAL ISCHEMIAR01NR007666 · NINR · UNIVERSITY OF ILLINOIS AT CHICAGO · PI BRIONES, TERESITA L · 2002 to 2006
$1.4M
NINR NIH HHS P30 NR000914NINR NIH HHS R01 NR007666
6 · The paper itself

Abstract

In the present study we examined whether vitamin D supplementation can reduce age-related tau hyperphosphorylation and cognitive impairment by enhancing brain energy homeostasis and protein phosphatase 2A (PP2A) activity, and modulating the redox state. Male F344 rats aged 20 months (aged) and 6 months (young) were randomly assigned to either vitamin D supplementation or no supplementation (control). Rats were housed in pairs and the supplementation group (n=10 young and n=10 aged) received subcutaneous injections of vitamin D (1, α25-dihydroxyvitamin D3) for 21 days. Control animals (n=10 young and n=10 aged) received equal volume of normal saline and behavioral testing in the water maze started on day 14 after the initiation of vitamin D supplementation. Tau phosphorylation, markers of brain energy metabolism (ADP/ATP ratio and adenosine monophosphate-activated protein kinase) and redox state (levels of reactive oxygen species, activity of superoxide dismutase, and glutathione levels) as well as PP2A activity were measured in hippocampal tissues. Our results extended previous findings that: (1) tau phosphorylation significantly increased during aging; (2) markers of brain energy metabolism and redox state are significantly decreased in aging; and (3) aged rats demonstrated significant learning and memory impairment. More importantly, we found that age-related changes in brain energy metabolism, redox state, and cognitive function were attenuated by vitamin D supplementation. No significant differences were seen in tau hyperphosphorylation, markers of energy metabolism and redox state in the young animal groups. Our data suggest that vitamin D ameliorated the age-related tau hyperphosphorylation and cognitive decline by enhancing brain energy metabolism, redox state, and PP2A activity making it a potentially useful therapeutic option to alleviate the effects of aging.

Indexed as

AgingAnimalsCalciumCognition DisordersDietary SupplementsEnergy MetabolismHippocampusHomeostasisMaleMaze LearningOxidation-ReductionPhosphorylationProtein Phosphatase 2Random AllocationRatsRats, Inbred F344CalciumProtein Phosphatase 2tau ProteinsVitamin DVitaminscognitive agingglutathionesuperoxide dismutasewater maze

Identifiers

PMID24412233
PMCPMC4103183
OpenAlexW2040180819

What OpenQuestion holds

Textmetadata
LicenceTDM
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.