Evidence map›Paper›PMID 30498985›Full record

ArticleJournal of molecular neuroscience : MN2019

Vasoactive Intestinal Peptide Decreases β-Amyloid Accumulation and Prevents Brain Atrophy in the 5xFAD Mouse Model of Alzheimer's Disease.

Orhan Tansel Korkmaz, Hakan Ay, Nurgul Aytan, Isabel Carreras, Neil W Kowall, Alpaslan Dedeoglu, Nese Tuncel

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of molecular neuroscience : MN, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

23 citing papers in PubMed, 31 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Endogenous VIP VPACBiology · 2022
    Article
  15. Article
  16. Protective effect of α-asarone and β-asarone on Aβ -induced inflammatory response in PC12 cells and its.Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2021
    Article
  17. Integration of lncRNA and mRNA profiles to reveal the protective effects ofInternational journal of molecular medicine · 2021
    Article
  18. Article
  19. Article
  20. 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

7 authors at 2 institutions in 2 countries.

Orhan Tansel KorkmazResearch and Development, VA Boston Healthcare System, Boston, MA, 02130, USA. tanselhan@gmail.com.ORCID http://orcid.org/0000-0003-1410-740X
Hakan AyDepartment of Anatomy, Faculty of Medicine, Eskisehir Osmangazi University, 26040, Eskisehir, Turkey.
Nurgul AytanResearch and Development, VA Boston Healthcare System, Boston, MA, 02130, USA.
Isabel CarrerasResearch and Development, VA Boston Healthcare System, Boston, MA, 02130, USA.
Neil W KowallResearch and Development, VA Boston Healthcare System, Boston, MA, 02130, USA.
Alpaslan DedeogluResearch and Development, VA Boston Healthcare System, Boston, MA, 02130, USA.
Nese TuncelDepartment of Physiology, Faculty of Medicine, Eskisehir Osmangazi University, 26480, Eskisehir, Turkey.
Boston University · USEskişehir Osmangazi University · TR

Funding

Neuropathology CoreP30AG013846 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI KOWALL, NEIL W. · 1996 to 2020
$29.1M
Cyclohexanehexol Therapy in Transgenic Models of Alzheimer's DiseaseR01AG031896 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI DEDEOGLU, ALPASLAN · 2009 to 2013
$1.9M
National Institute on Aging P30AG013846NIA NIH HHS R01AG031896Türkiye Bilimsel ve Teknolojik Araştirma Kurumu 1059B190900502
6 · The paper itself

Abstract

Alzheimer's disease (AD) is a neurodegenerative disorder characterized by extracellular deposits of fibrillary β-amyloid (Aβ) plaques in the brain that initiate an inflammatory process resulting in neurodegeneration. The neuronal loss associated with AD results in gross atrophy of affected regions causing a progressive loss of cognitive ability and memory function, ultimately leading to dementia. Growing evidence suggests that vasoactive intestinal peptide (VIP) could be beneficial for various neurodegenerative diseases, including AD. The study investigated the effects of VIP on 5xFAD, a transgenic mouse model of AD. Toward this aim, we used 20 5xFAD mice in two groups (n = 10 each), VIP-treated (25 ng/kg i.p. injection, three times per week) and saline-treated (the drug's vehicle) following the same administration regimen. Treatment started at 1 month of age and ended 2 months later. After 2 months of treatment, the mice were euthanized, their brains dissected out, and immunohistochemically stained for Aβ

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesAnimalsAtrophyBrainFemaleMiceNeuroprotective AgentsVasoactive Intestinal PeptideAmyloid beta-PeptidesNeuroprotective AgentsVasoactive Intestinal Peptide5xFADAlzheimer’s diseaseBrain atrophyNeuroinflammationVasoactive intestinal peptideβ-Amyloid plaques

Identifiers

PMID30498985
OpenAlexW2902678191

What OpenQuestion holds

Textmetadata
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.