Evidence map›Paper›PMID 24513404›Full record

ArticleBrain research2014

Short-term effects of an endotoxin on substantia nigra dopamine neurons.

Kaela R S Reinert, Claudia D Umphlet, Ariana Quattlebaum, Heather A Boger

Abstract read
In one paragraph

Article in Brain research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Inflammatory Animal Models of Parkinson's Disease.Journal of Parkinson's disease · 2022
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Inflammation Effects on Motivation and Motor Activity: Role of Dopamine.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2017
    Review
  16. Article
  17. Review
  18. 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

4 authors at 1 institution in 1 country.

Kaela R S ReinertDepartment of Neurosciences and Center on Aging, Medical University of South Carolina, 173 Ashley Ave, BSB Suite 403, MSC 510, Charleston, SC 29425, USA.
Claudia D UmphletDepartment of Neurosciences and Center on Aging, Medical University of South Carolina, 173 Ashley Ave, BSB Suite 403, MSC 510, Charleston, SC 29425, USA.
Ariana QuattlebaumDepartment of Neurosciences and Center on Aging, Medical University of South Carolina, 173 Ashley Ave, BSB Suite 403, MSC 510, Charleston, SC 29425, USA.
Heather A BogerDepartment of Neurosciences and Center on Aging, Medical University of South Carolina, 173 Ashley Ave, BSB Suite 403, MSC 510, Charleston, SC 29425, USA. Electronic address: boger@musc.edu.
Medical University of South Carolina · US

Funding

NEUROINFLAMMATION AND THE AGED DOPINERGIC SYSTEMP01AG023630 · NIA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI GRANHOLM-BENTLEY, ANN-CHARLOTTE ESTHER · 2005 to 2011
$5.3M
Oxidative Stress and Glutamate Excitotoxicity on Aged Dopaminergic NeruonsK99AG033687 · NIA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BOGER, HEATHER A · 2009 to 2010
$140k
NIA NIH HHS AG023630NIA NIH HHS K99 AG033687NIA NIH HHS P01 AG023630
6 · The paper itself

Abstract

Inflammation has been implicated in the pathology of several neurodegenerative diseases, including Parkinson׳s disease (PD). Studies using the endotoxin lipopolysaccharide (LPS), a potent inflammogen, show that systemic insults can trigger prolonged microglial activation and pro-inflammatory cytokine production leading to degeneration of substantia nigra (SN) dopamine (DA) neurons, mimicking idiopathic PD. Because rapid effects of LPS on SN neurons had not been investigated previously, the focus of this study is to assess time-dependent alterations in SN neuroinflammation, DAergic neurons, and neuronal signaling cascades following LPS administration. LPS (5mg/kg, i.p.) or saline (0.9% NaCl) was administered to 8-month-old male mice. At 3h, 5h, and 12h post-injection, the morphology of the SN was assessed using antibodies directed against tyrosine hydroxylase (TH, DAergic marker), Iba-1 (pan-microglial marker), phospho-ERK, and phospho-CREB (signaling). LPS administration significantly reduced TH-immunoreactivity (ir) at all time-points with the greatest reduction observed at 12h post-injection. Reduced TH-ir was accompanied by a significant increase in activated microglia at all time-points following LPS. By 12h post-injection, LPS-treated mice exhibited activated as well as reactive microglia, which can result in neuronal damage. These data demonstrate that the initial reduction in TH-ir observed after an LPS injection was not concomitant with morphological alterations in microglial cells, even though a significant increase in phospho-ERK was observed in glial cells as soon as 3h post-injection. It is possible that the initial alteration in DA phenotype (TH reduction) may perpetuate an inflammatory response that persists and leads to further DAergic damage.

Indexed as

AnimalsCalcium-Binding ProteinsCyclic AMP Response Element-Binding ProteinEndotoxinsExtracellular Signal-Regulated MAP KinasesImmunohistochemistryLipopolysaccharidesMaleMiceMice, Inbred C57BLMicrofilament ProteinsMicrogliaNeurogliaNeuroimmunomodulationNeuronsPhosphorylationAif1 protein, mouseCalcium-Binding ProteinsCyclic AMP Response Element-Binding ProteinEndotoxinsExtracellular Signal-Regulated MAP KinasesLipopolysaccharidesMicrofilament ProteinsTyrosine 3-MonooxygenaseDopamineInflammationLipopolysaccharideSubstantia nigra

Identifiers

PMID24513404
PMCPMC3970422
OpenAlexW2006754174

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.