Evidence map›Paper›PMID 29774542›Full record

ArticleThe Journal of pathology2018

Accelerated pre-senile systemic amyloidosis in PACAP knockout mice - a protective role of PACAP in age-related degenerative processes.

Dora Reglodi, Adel Jungling, Rémi Longuespée, Joerg Kriegsmann, Rita Casadonte, Mark Kriegsmann, Tamas Juhasz, Sebastian Bardosi, Andrea Tamas, Balazs Daniel Fulop and 7 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

27 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Diagnostic and Prognostic Value of PACAP in Multiple Myeloma.International journal of molecular sciences · 2023
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. PACAP for Retinal Health: Model for Cellular Aging and Rescue.International journal of molecular sciences · 2021
    Article
  13. Review
  14. Article
  15. Probing theFrontiers in neuroscience · 2021
    Review
  16. Alzheimer's Disease Mouse as a Model of Testis Degeneration.International journal of molecular sciences · 2020
    Article
  17. Article
  18. Protective Effects of PACAP in Peripheral Organs.Frontiers in endocrinology · 2020
    Review
  19. Article
  20. 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

17 authors at 6 institutions in 4 countries.

Dora ReglodiDepartment of Anatomy, MTA-PTE PACAP Research Group, University of Pecs Medical School, Pécs, Hungary.
Adel JunglingDepartment of Anatomy, MTA-PTE PACAP Research Group, University of Pecs Medical School, Pécs, Hungary.
Rémi LonguespéeInstitute of Pathology, University of Heidelberg, Heidelberg, Germany.
Joerg KriegsmannCenter for Histology, Cytology and Molecular Diagnostics, Trier, Germany.
Rita CasadonteProteopath GmbH, Trier, Germany.
Mark KriegsmannInstitute of Pathology, University of Heidelberg, Heidelberg, Germany.ORCID 0000-0002-7319-3646
Tamas JuhaszDepartment of Anatomy, Histology and Embryology, Faculty of Medicine, University of Debrecen, Hungary.
Sebastian BardosiCenter for Histology, Cytology and Molecular Diagnostics, Trier, Germany.
Andrea TamasDepartment of Anatomy, MTA-PTE PACAP Research Group, University of Pecs Medical School, Pécs, Hungary.
Balazs Daniel FulopDepartment of Anatomy, MTA-PTE PACAP Research Group, University of Pecs Medical School, Pécs, Hungary.
Krisztina KovacsDepartment of Biochemistry and Medical Chemistry, University of Pecs Medical School, Pécs, Hungary.
Zsuzsanna NagySecond Department of Internal Medicine, University of Pecs Medical School, Pécs, Hungary.
Jason SparksDepartment of Anatomy, MTA-PTE PACAP Research Group, University of Pecs Medical School, Pécs, Hungary.
Attila MisetaDepartment of Laboratory Medicine and Szentagothai Research Centre, University of Pecs Medical School, Pécs, Hungary.
Gabriel MazzucchelliLaboratory of Mass Spectrometry (LSM) - MolSys, Department of Chemistry, University of Liège, Belgium.
Hitoshi HashimotoLaboratory of Molecular Neuropharmacology, Graduate School of Pharmaceutical Sciences, Osaka University, Japan.
Attila BardosiCenter for Histology, Cytology and Molecular Diagnostics, Trier, Germany.ORCID 0000-0002-2791-7017
University of Pecs · HUUniversität Trier · DEHeidelberg University · DEOsaka University of Pharmaceutical Sciences · JPUniversity of Debrecen · HUUniversity of Liège · BE

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. Among them, pituitary adenylate cyclase-activating polypeptide (PACAP) is a potent cytoprotective peptide that provides an endogenous control against a variety of tissue-damaging stimuli. We hypothesized that the progressive decline of PACAP throughout life and the well-known general cytoprotective effects of PACAP lead to age-related pathophysiological changes in PACAP deficiency, supported by the increased vulnerability to various stressors of animals partially or totally lacking PACAP. Using young and aging CD1 PACAP knockout (KO) and wild type (WT) mice, we demonstrated pre-senile amyloidosis in young PACAP KO animals and showed that senile amyloidosis appeared accelerated, more generalized, more severe, and affected more individuals. Histopathology showed age-related systemic amyloidosis with mainly kidney, spleen, liver, skin, thyroid, intestinal, tracheal, and esophageal involvement. Mass spectrometry-based proteomic analysis, reconfirmed with immunohistochemistry, revealed that apolipoprotein-AIV was the main amyloid protein in the deposits together with several accompanying proteins. Although the local amyloidogenic protein expression was disturbed in KO animals, no difference was found in laboratory lipid parameters, suggesting a complex pathway leading to increased age-related degeneration with amyloid deposits in the absence of PACAP. In spite of no marked inflammatory histological changes or blood test parameters, we detected a disturbed cytokine profile that possibly creates a pro-inflammatory milieu favoring amyloid deposition. In summary, here we describe accelerated systemic senile amyloidosis in PACAP gene-deficient mice, which might indicate an early aging phenomenon in this mouse strain. Thus, PACAP KO mice could serve as a model of accelerated aging with human relevance. © 2018 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.

Indexed as

Plaque, AmyloidAge FactorsAmyloidosisAnimalsApolipoproteins ACytokinesDisease Models, AnimalDisease ProgressionGenetic Predisposition to DiseaseInflammation MediatorsMice, KnockoutPhenotypePituitary Adenylate Cyclase-Activating PolypeptideProteomicsSeverity of Illness IndexSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationAdcyap1 protein, mouseapolipoprotein A-IVApolipoproteins ACytokinesInflammation MediatorsPituitary Adenylate Cyclase-Activating Polypeptideamyloidapolipoprotein-AIVMALDI imagingproteomic analysis

Identifiers

PMID29774542
PMCPMC6055756
OpenAlexW2892180966

What OpenQuestion holds

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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.