Evidence map›Paper›PMID 19664623›Full record

ArticleExperimental neurology2009

Alpha-synuclein immunopositive aggregates in the myenteric plexus of the aging Fischer 344 rat.

Robert J Phillips, Gary C Walter, Brittany E Ringer, Katherine M Higgs, Terry L Powley

Open access · greenAbstract read
In one paragraph

Article in Experimental neurology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 10% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 67 citations in OpenAlex.

  1. Impact of aging on animal models of Parkinson's disease.Frontiers in aging neuroscience · 2022
    Pooled it
  2. Trial
  3. Review
  4. Article
  5. Review
  6. Review
  7. The Aging Enteric Nervous System.International journal of molecular sciences · 2023
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Parkinson's Disease: A Prionopathy?International journal of molecular sciences · 2021
    Review
  17. Review
  18. Article
  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

5 authors at 1 institution in 1 country.

Robert J PhillipsPurdue University, Department of Psychological Sciences, 703 Third Street, West Lafayette, IN 47907-2081, USA. rphillip@psych.purdue.edu
Gary C Walter
Brittany E Ringer
Katherine M Higgs
Terry L Powley
Purdue University West Lafayette · US

Funding

HYPOTHALAMIC CONTROL OF BODY WEIGHT AND FEEDINGR01DK027627 · NIDDK · PURDUE UNIVERSITY WEST LAFAYETTE · PI POWLEY, TERRY L. · 1986 to 2021
$6.1M
Autonomic Control of Body Weight and FeedingR37DK027627 · NIDDK · PURDUE UNIVERSITY · PI POWLEY, TERRY L. · 2007 to 2016
$5.5M
Gastrointestinal Tract Innervation: Patterns of AgingR01DK061317 · NIDDK · PURDUE UNIVERSITY WEST LAFAYETTE · PI POWLEY, TERRY L. · 2002 to 2012
$3.1M
NIDDK NIH HHS DK27627NIDDK NIH HHS DK61317NIDDK NIH HHS R01 DK027627NIDDK NIH HHS R01 DK061317NIDDK NIH HHS R37 DK027627
6 · The paper itself

Abstract

Dystrophic axons and terminals are common in the myenteric plexus and smooth muscle of the gastrointestinal (GI) tract of aged rats. In young adult rats, alpha-synuclein in its normal state is abundant throughout the myenteric plexus, making this protein-which is prone to fibrillization-a candidate marker for axonopathies in the aged rat. To determine if aggregation of alpha-synuclein is involved in the formation of age-related enteric neuropathies, we sampled the stomach, small intestine and large intestine of adult, middle-aged, and aged virgin male Fischer 344 rats stained for alpha-synuclein in both its normal and pathological states. Alpha-synuclein-positive dystrophic axons and terminals were present throughout the GI tract of middle-aged and aged rats, with immunohistochemical double labeling demonstrating co-localization within nitric oxide synthase-, calretinin-, calbindin-, or tyrosine hydroxylase-positive markedly swollen neurites. However, other dystrophic neurites positive for each of these four markers were not co-reactive for alpha-synuclein. Similarly, a subpopulation of alpha-synuclein inclusions contained deposits immunostained with an anti-tau phospho-specific Ser(262) antibody, but not all of these hyperphosphorylated tau-positive aggregates were co-localized with alpha-synuclein. The presence of heteroplastic and potentially degenerating neural elements and protein aggregates both positive and negative for alpha-synuclein suggests a complex chronological relationship between the onset of degenerative changes and the accumulation of misfolded proteins. Additionally, proteins other than alpha-synuclein appear to be involved in age-related axonopathies. Finally, this study establishes the utility of the aging Fischer 344 rat for the study of synucleopathies and tauopathies in the GI tract.

Indexed as

Agingalpha-SynucleinAnimalsAutonomic Nervous System DiseasesAxonsBiomarkersCalcium-Binding ProteinsGastrointestinal TractImmunohistochemistryLewy BodiesMaleMyenteric PlexusNitric Oxide Synthase Type IProtein FoldingRatsRats, Inbred F344alpha-SynucleinBiomarkersCalcium-Binding ProteinsNitric Oxide Synthase Type Itau ProteinsTyrosine 3-Monooxygenase

Identifiers

PMID19664623
PMCPMC2761519
OpenAlexW2073114676

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.