Evidence map›Paper›PMID 30345481›Full record

ReviewGeroScience2018

PACAP deficiency as a model of aging.

D Reglodi, T Atlasz, E Szabo, A Jungling, A Tamas, T Juhasz, B D Fulop, A Bardosi

Open access · greenAbstract readReview
In one paragraph

Review in GeroScience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
3.6field-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

48 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
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  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Diagnostic and Prognostic Value of PACAP in Multiple Myeloma.International journal of molecular sciences · 2023
    Article
  11. Role of endocrine PACAP in age-related diseases.Frontiers in endocrinology · 2023
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  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

8 authors at 2 institutions in 1 country.

D ReglodiDepartment of Anatomy, MTA-PTE PACAP Research Group, University of Pecs Medical School, Pecs, Hungary. dora.reglodi@aok.pte.hu.
T AtlaszDepartment of Anatomy, MTA-PTE PACAP Research Group, University of Pecs Medical School, Pecs, Hungary.
E SzaboDepartment of Anatomy, MTA-PTE PACAP Research Group, University of Pecs Medical School, Pecs, Hungary.
A JunglingDepartment of Anatomy, MTA-PTE PACAP Research Group, University of Pecs Medical School, Pecs, Hungary.
A TamasDepartment of Anatomy, MTA-PTE PACAP Research Group, University of Pecs Medical School, Pecs, Hungary.
T JuhaszDepartment of Anatomy, Histology and Embryology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
B D FulopDepartment of Anatomy, MTA-PTE PACAP Research Group, University of Pecs Medical School, Pecs, Hungary.
A BardosiCenter for Histology, Cytology and Molecular Diagnostics, and Proteopath GmbH, Trier, Germany.
University of Pecs · HUUniversity of Debrecen · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dysregulation of neuropeptides may play an important role in aging-induced impairments. In the long list of neuropeptides, pituitary adenylate cyclase-activating polypeptide (PACAP) represents a highly effective cytoprotective peptide that provides an endogenous control against a variety of tissue-damaging stimuli. PACAP has neuro- and general cytoprotective effects due to anti-apoptotic, anti-inflammatory, and antioxidant actions. As PACAP is also a part of the endogenous protective machinery, it can be hypothesized that the decreased protective effects in lack of endogenous PACAP would accelerate age-related degeneration and PACAP knockout mice would display age-related degenerative signs earlier. Recent results support this hypothesis showing that PACAP deficiency mimics aspects of age-related pathophysiological changes including increased neuronal vulnerability and systemic degeneration accompanied by increased apoptosis, oxidative stress, and inflammation. Decrease in PACAP expression has been shown in different species from invertebrates to humans. PACAP-deficient mice display numerous pathological alterations mimicking early aging, such as retinal changes, corneal keratinization and blurring, and systemic amyloidosis. In the present review, we summarize these findings and propose that PACAP deficiency could be a good model of premature aging.

Indexed as

AgingAnimalsMiceModels, AnimalPituitary Adenylate Cyclase-Activating PolypeptidePituitary Adenylate Cyclase-Activating PolypeptideAgingAmyloidosisApoptosisDegenerationPACAP

Identifiers

PMID30345481
PMCPMC6294727
OpenAlexW2897815863

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.