Evidence map›Paper›PMID 25269834›Full record

ArticleBrain structure & function2016

Mapping dopaminergic deficiencies in the substantia nigra/ventral tegmental area in schizophrenia.

Matthew W Rice, Rosalinda C Roberts, Miguel Melendez-Ferro, Emma Perez-Costas

Abstract read
In one paragraph

Article in Brain structure & function, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.0field-weighted citation impact, top 31% 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

24 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
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  5. Atypical antipsychotics antagonize GABAMolecular psychiatry · 2023
    Article
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  11. Review
  12. Review
  13. Article
  14. Evidence for altered excitatory and inhibitory tone in the post-mortem substantia nigra in schizophrenia.The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry · 2020
    Article
  15. Article
  16. Article
  17. Article
  18. Neuromelanin-sensitive MRI as a noninvasive proxy measure of dopamine function in the human brain.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  19. Article
  20. 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.

Matthew W RiceDepartment of Psychology, University of Alabama at Birmingham, Campbell Hall 415, 1720 2nd Avenue South, Birmingham, AL, 35294, USA.
Rosalinda C RobertsDepartment of Psychiatry and Behavioral Neurobiology, University of Alabama at Birmingham, Birmingham, USA.
Miguel Melendez-FerroDepartment of Psychology, University of Alabama at Birmingham, Campbell Hall 415, 1720 2nd Avenue South, Birmingham, AL, 35294, USA.
Emma Perez-CostasDepartment of Psychology, University of Alabama at Birmingham, Campbell Hall 415, 1720 2nd Avenue South, Birmingham, AL, 35294, USA. epcostas@gmail.com.
University of Alabama at Birmingham · US

Funding

NEUROPATHOLOGY OF DOPAMINE SYSTEMS IN SCHIZOPHRENIAR01MH066123 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI ROBERTS, ROSALINDA C · 2003 to 2015
$3.6M
NIMH NIH HHS R01 MH066123NIMH NIH HHS R01MH066123-09
6 · The paper itself

Abstract

Previous work from our laboratory showed deficits in tyrosine hydroxylase protein expression within the substantia nigra/ventral tegmental area (SN/VTA) in schizophrenia. However, little is known about the nature and specific location of these deficits within the SN/VTA. The present study had two aims: (1) test if tyrosine hydroxylase deficits could be explained as the result of neuronal loss; (2) assess if deficits in tyrosine hydroxylase are sub-region specific within the SN/VTA, and thus, could affect specific dopaminergic pathways. To achieve these objectives: (1) we obtained estimates of the number of dopaminergic neurons, total number of neurons, and their ratio in matched SN/VTA schizophrenia and control samples; (2) we performed a qualitative assessment in SN/VTA schizophrenia and control matched samples that were processed simultaneously for tyrosine hydroxylase immunohistochemistry. We did not find any significant differences in the total number of neurons, dopaminergic neurons, or their ratio. Our qualitative study of TH expression showed a conspicuous decrease in labeling of neuronal processes and cell bodies within the SN/VTA, which was sub-region specific. Dorsal diencephalic dopaminergic populations of the SN/VTA presented the most conspicuous decrease in TH labeling. These data support the existence of pathway-specific dopaminergic deficits that would affect the dopamine input to the cortex without significant neuronal loss. Interestingly, these findings support earlier reports of decreases in tyrosine hydroxylase labeling in the target areas for this dopaminergic input in the prefrontal and entorhinal cortex. Finally, our findings support that tyrosine hydroxylase deficits could contribute to the hypodopaminergic state observed in cortical areas in schizophrenia.

Indexed as

AdultAgedAged, 80 and overCell CountDopamineDopaminergic NeuronsFemaleHumansMaleMiddle AgedSchizophreniaSubstantia NigraTyrosine 3-MonooxygenaseVentral Tegmental AreaDopamineTyrosine 3-MonooxygenaseImmunohistochemistryMesocorticalMesolimbicNeuropathologyNeuropsychiatric disordersTyrosine hydroxylase

Identifiers

PMID25269834
PMCPMC4504823
OpenAlexW1985518842

What OpenQuestion holds

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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.