Evidence map›Paper›PMID 15897154›Full record

ReviewNeurotoxicity research2005

MPTP and SNpc DA neuronal vulnerability: role of dopamine, superoxide and nitric oxide in neurotoxicity. Minireview.

V Jackson-Lewis, R J Smeyne

Abstract readReview
PubMed Publisher
In one paragraph

Review in Neurotoxicity research, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

37 citing papers in PubMed, 76 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Renal Dopamine Oxidation and Inflammation in High Salt Fed Rats.Journal of the American Heart Association · 2020
    Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Redox Imbalance and Viral Infections in Neurodegenerative Diseases.Oxidative medicine and cellular longevity · 2016
    Review
  12. Article
  13. Article
  14. Oxidative stress and Parkinson's disease.Frontiers in neuroanatomy · 2015
    Review
  15. Review
  16. Review
  17. Article
  18. Suppression of inflammation with conditional deletion of the prostaglandin E2 EP2 receptor in macrophages and brain microglia.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    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

2 authors at 2 institutions in 1 country.

V Jackson-LewisNeuroscience Research Laboratories of Movement Disorders Division, Department of Neurology, Columbia University, New York, NY 10032, USA. vrj1@columbia.edu
R J Smeyne
Columbia University · USSt. Jude Children's Research Hospital · US

Funding

GENETICS OF MPTP-INDUCED PARKINSONISMR01NS039006 · NINDS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI SMEYNE, RICHARD J · 1999 to 2009
$2.2M
ROLE OF GLIA IN PARKINSON'S DISEASER01ES010772 · NIEHS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI MORGAN, JAMES I · 2000 to 2004
$1.4M
NIEHS NIH HHS ES10772NINDS NIH HHS NS39006
6 · The paper itself

Abstract

Parkinson disease (PD) is a common neurodegenerative disease of unknown origin that is characterized, mainly, by a significant reduction in the number of dopamine neurons in the substantia nigra pars compacta (SNpc) of the brain and a dramatic reduction in dopamine levels in the corpus striatum. For reasons that we do not know, the dopamine neuron seems to be more vulnerable to damage than any other neuron in the brain. Although hypotheses of damage to the dopamine neuron include oxidative stress, growth factor decline, excitotoxicity, inflammation in the SNpc and protein aggregation, oxidative stress in the nigrostriatal dopaminergic system garners a significant amount of attention. In the oxidative stress hypothesis of PD, superoxide, nitric oxide and dopamine all conspire to create an environment that can be detrimental to the dopamine neuron. MPTP (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine), the tool of choice for investigations into the mechanisms involved in the death of dopamine neurons in PD, has been used extensively in attempts to sort out what happens in and around the dopamine neuron. Herein, we review the roles of dopamine, superoxide and nitric oxide in the demise of the dopamine neuron in the MPTP model of PD as it relates to the death of the dopamine neuron noted in PD.

Indexed as

1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridineAnimalsDopamineEnvironmentHumansNeural Networks, ComputerNeurogliaNeuronsNitric OxideSubstantia NigraSuperoxides1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridineDopamineNitric OxideSuperoxides

Identifiers

PMID15897154
OpenAlexW2093832364

What OpenQuestion holds

Textmetadata
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.