Evidence map›Paper›PMID 24060432›Full record

ArticleToxicology2013

Evaluation of neurobehavioral and neuroinflammatory end-points in the post-exposure period in rats sub-acutely exposed to manganese.

Dinamene Santos, Santos Dinamene, M Camila Batoréu, Batoreu M Camila, I Tavares de Almeida, L Davis Randall, M Luísa Mateus, Mateus M Luisa, Vanda Andrade, Andrade Vanda and 8 more

Erratum issuedAbstract read
In one paragraph

Article in Toxicology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Magnetic resonance imaging to assess the brain response to fasting in glioblastoma-bearing rats as a model of cancer anorexia.Cancer imaging : the official publication of the International Cancer Imaging Society · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Severity of parkinsonism associated with environmental manganese exposure.Environmental health : a global access science source · 2021
    Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Manganese-induced Neurotoxicity: FromToxicology research · 2015
    Article
4 · The record

Corrections and comments

  • Erratum issued
    Dinamene, Santos [corrected to Santos, Dinamene]; Camila, Batoreu M [corrected to Batoréu, M Camila]; Luisa, Mateus [corrected to Mateus, M Luísa]; Vanda, Andrade [corrected to Andrade, Vanda]; Ruben, Ramos [corrected to Ramos, Ruben]; Edite, Torres [cor
5 · Who and what money

Authors and funding

18 authors.

Dinamene Santos
Santos DinameneI-Med.UL, Department of Toxicology and Food Sciences, Faculty of Pharmacy, University of Lisbon, Lisbon, Portugal.
M Camila Batoréu
Batoreu M Camila
I Tavares de Almeida
L Davis Randall
M Luísa Mateus
Mateus M Luisa
Vanda Andrade
Andrade Vanda
Ruben Ramos
Ramos Ruben
Edite Torres
Torres Edite
Michael Aschner
Aschner Michael
A P Marreilha dos Santos
A P Marreilha Dos Santos

Funding

Mechanisms of Manganese NeurotoxicityR01ES010563 · NIEHS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Michael Aschner, Aaron B Bowman · 2001 to 2026
$11.9M
NIEHS NIH HHS R01 ES010563
6 · The paper itself

Abstract

Manganese (Mn) can cause manganism, a neurological disorder similar to Parkinson' Disease (PD). The neurobehavioral and neuroinflammatory end-points in the Mn post exposure period have not been studied yet. Rats were injected on alternate days with 8 doses of MnCl2 (25mg/kg) or saline, then euthanized 1, 10, 30 or 70 days following the last dose. Whole-blood (WB) (p<0.05), urine (p<0.05) and brain cortical (p<0.0001) Mn levels were significantly increased 24h after the last dose. Decreases in the rats' ambulation were noted 1, 10 and 30 days after the last Mn dose (p<0.001; p<0.05; p<0.001, respectively) and also in the rearing activity at the four time-points (p<0.05). Cortical glial fibrillary acid protein immunoreactivity (GFAP-ir) was significantly increased at 1, 10, 30 (p<0.0001) and 70 (p<0.001) days after the last Mn dose, as well as tumor necrosis α (TNF-α) levels (p<0.05) but just on day 1. Taken together, the results show that, during the 70-day clearance phase of Mn, the recovery is not immediate as behavioral alterations and neuroinflammation persist long after Mn is cleared from the cortical brain compartment.

Indexed as

AnimalsBehavior, AnimalBrainCerebral CortexChloridesDose-Response Relationship, DrugEndpoint DeterminationGlial Fibrillary Acidic ProteinImmunohistochemistryInflammationMaleManganeseManganese CompoundsManganese PoisoningMotor ActivityRatsChloridesGlial Fibrillary Acidic ProteinManganesemanganese chlorideManganese CompoundsGFAPManganese neurotoxicityNeurobehavioral assaysNeuroinflammationTNF-α

Identifiers

PMID24060432
PMCPMC3850178

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Registered trials

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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.