Evidence map›Paper›PMID 23726958›Full record

ReviewExperimental neurology2014

A survey from 2012 of evidence for the role of neuroinflammation in neurotoxin animal models of Parkinson's disease and potential molecular targets.

Chenere P Ramsey, Malú G Tansey

Abstract readReview
In one paragraph

Review in Experimental neurology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 8% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Pooled it
  2. Article
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  4. Article
  5. Anti-Neuroinflammatory Effect of Ombuin fromInternational journal of molecular sciences · 2024
    Article
  6. Review
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  11. Investigation of the peripheral inflammation (neutrophil-lymphocyte ratio) in two neurodegenerative diseases of the central nervous system.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2022
    Article
  12. Article
  13. [Regulatory mechanism of interferon regulatory factor 1 byNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2021
    Article
  14. Review
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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

2 authors at 1 institution in 1 country.

Chenere P RamseyDepartment of Physiology, School of Medicine, Emory University, Atlanta, GA, USA; Department of Biological Sciences, School of Science, Hampton University, Hampton, VA, USA.
Malú G TanseyDepartment of Physiology, School of Medicine, Emory University, Atlanta, GA, USA. Electronic address: malu.tansey@emory.edu.
Emory University · US

Funding

IRACDA Fellowships in Research and Science Training (FIRST)K12GM000680 · NIGMS · EMORY UNIVERSITY · PI BROWN, LOU ANN S, MCCARTY, NAEL A · 2000 to 2024
$41.2M
The Emory Alzheimer's Disease CenterP50AG025688 · NIA · EMORY UNIVERSITY · PI LEVEY, ALLAN I · 2005 to 2019
$25.7M
Graduate and Postdoctoral Training in ToxicologyT32ES012870 · NIEHS · EMORY UNIVERSITY · PI Carmen Joseph Marsit · 2004 to 2026
$9.1M
PROJECT 3: METABOLOMIC BIOMARKERS OF PARKINSON'S DISEASEP01ES016731 · NIEHS · EMORY UNIVERSITY · PI MILLER, GARY W · 2008 to 2012
$6.7M
TRAINING IN TRANSLATIONAL RESEARCH IN NEUROLOGYT32NS007480 · NINDS · EMORY UNIVERSITY · PI LEVEY, ALLAN I · 2000 to 2020
$4.5M
RGS10 in microglia activation and dopaminergic neuron survivalR01NS072467 · NINDS · EMORY UNIVERSITY · PI TANSEY, MARIA DE LOURDES GAMEZ · 2010 to 2014
$1.7M
NIA NIH HHS P50 AG025688NIEHS NIH HHS 5P01ES016731NIEHS NIH HHS P01 ES016731NIEHS NIH HHS T32 ES012870NIGMS NIH HHS 5K12GM000680NIGMS NIH HHS K12 GM000680NINDS NIH HHS 5R01NS072467NINDS NIH HHS 5T32NS007480NINDS NIH HHS R01 NS072467NINDS NIH HHS T32 NS007480
6 · The paper itself

Abstract

Parkinson's disease (PD) is a neurodegenerative movement disorder that results from the progressive loss of dopaminergic neurons in the midbrain substantia nigra pars compacta (SNpc). The specific molecular events that cause PD are currently not known; however, progress to better understand PD pathogenesis has been made using various animal models of the disease. In this review, we have highlighted reports from 2012 in which neurochemical/neurotoxins have been used in rodents to specifically address the role of neuroinflammation in the development and/or progression of PD-like pathology and in particular nigral degeneration. A number of studies have been summarized in which plausible pro-inflammatory, anti-inflammatory, or therapeutic agents targeting inflammatory pathways were introduced and/or investigated by various groups for neuroprotective effects. From these studies, it is clear that neuroinflammation acts to exacerbate the toxic outcomes that are set in motion within neurons following exposure to neurotoxins. Additionally, it is noted that future work is still needed to better understand the underlying mechanisms mediating the neuroinflammatory and neurotoxic phenotypes reported in rodent models of PD-like pathology to maximize the translation potential of these interventions to the clinic to prevent and/or delay PD onset and/or progression in humans.

Indexed as

AnimalsDisease Models, AnimalDopamineInflammationNerve DegenerationNeuronsParkinson Disease, SecondarySubstantia NigraDopamine6-OHDADopaminergicLPSMicrogliaMPTPNeurodegenerationNeuroinflammationNeurotoxinNigrostriatalParaquatParkinson's disease

Identifiers

PMID23726958
PMCPMC3823748
OpenAlexW1969604768

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.