Evidence map›Paper›PMID 20307667›Full record

ArticleNeurobiology of disease2010

Neuron-selective changes in RNA transcripts related to energy metabolism in toxic models of parkinsonism in rodents.

James G Greene, Raymond Dingledine, J Timothy Greenamyre

Open access · greenAbstract read
In one paragraph

Article in Neurobiology of disease, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. 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

3 authors at 2 institutions in 1 country.

James G GreeneDepartments of Neurology and Pharmacology, and the Center for Neurodegenerative Disease, Emory University School of Medicine, Atlanta, GA, USA. jggreen@emory.edu <jggreen@emory.edu>
Raymond Dingledine
J Timothy Greenamyre
Emory University · USUniversity of Pittsburgh · US

Funding

Molecular mechanism of selective neuronal vulnerabilityK08NS048858 · NINDS · EMORY UNIVERSITY · PI GREENE, JAMES G · 2005 to 2009
$837k
NINDS NIH HHS K08 NS048858NINDS NIH HHS NINDS K08 NS048858
6 · The paper itself

Abstract

Dopamine (DA) neurons in the substantia nigra (SNDA neurons) are among the most severely affected in Parkinson's disease (PD). Mitochondrial complex I inhibition by rotenone or MPTP can induce SNDA neurodegeneration and recapitulate motor disability in rodents. We performed a transcriptional analysis of the midbrain response to complex I inhibition focused on selected metabolic transcripts using quantitative real-time RT-PCR in conjunction with laser-capture microdissection (LCM) of immunofluorescently targeted SNDA and ventral tegmental area (VTA) DA neurons. There were DA neuron-selective alterations in metabolic transcripts in response to generalized complex I inhibition dependent on the behavioral response of the animal, and vulnerable SNDA neurons were more dynamic in their metabolic transcriptional response than less vulnerable VTADA neurons. The metabolic transcriptional response of DA neurons may contribute significantly to the ultimate toxicity associated with mitochondrial inhibition, and better understanding of this response may provide insight into potential targets for neuroprotection in PD.

Indexed as

AnimalsDisease Models, AnimalDopamineElectron Transport Complex IMaleMesencephalonMiceMice, Inbred C57BLMicrodissectionNeuronsParkinsonian DisordersRatsRats, Inbred LewReverse Transcriptase Polymerase Chain ReactionRNASubstantia NigraDopamineElectron Transport Complex IRNA

Identifiers

PMID20307667
PMCPMC2872119
OpenAlexW2134106974

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.