Evidence map›Paper›PMID 19474310›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2009

Dopamine depletion induces distinct compensatory gene expression changes in DARPP-32 signal transduction cascades of striatonigral and striatopallidal neurons.

Bernhard H Meurers, Gustavo Dziewczapolski, Tao Shi, Anton Bittner, Fredrik Kamme, Clifford W Shults

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
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  6. Gene expression analyses identify Narp contribution in the development of L-DOPA-induced dyskinesia.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  7. FACS array profiling identifies Ecto-5' nucleotidase as a striatopallidal neuron-specific gene involved in striatal-dependent learning.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
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  14. Article
  15. Modulation of striatal projection systems by dopamine.Annual review of neuroscience · 2011
    Review
  16. Article
  17. 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

6 authors at 3 institutions in 1 country.

Bernhard H MeurersDepartment of Neurology, The David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California 90095, USA. bmeurers@ljmail.net
Gustavo Dziewczapolski
Tao Shi
Anton Bittner
Fredrik Kamme
Clifford W Shults
Johnson & Johnson (United States) · USUniversity of California, San Diego · USUniversity of California, Los Angeles · US

Funding

Studies on Diagnosis, Pathophysiology, and Treatment of Autonomic Failure in MSAP01NS044233 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LOW, PHILLIP A · 2003 to 2014
$12.4M
NINDS NIH HHS P01 NS044233
6 · The paper itself

Abstract

Functional alterations in striatal projection neurons play a critical role in the development of motor symptoms in Parkinson's disease (PD), but their molecular adaptation to dopamine depletion remains poorly understood. In particular, type and extent of regulation in postsynaptic signal transduction pathways that determine the responsiveness of striatal projection neurons to incoming stimuli, are currently unknown. Using cell-type-specific transcriptome analyses in a rodent model of chronic dopamine depletion, we identified large-scale gene expression changes, including neurotransmitter receptors, signal transduction cascades, and target proteins of dopamine signaling in striatonigral and striatopallidal neurons. Within the dopamine- and cAMP-regulated phosphoprotein of 32 kDa (DARPP-32) cascade of enzymes that plays a central role in signal integration of dopaminoceptive neurons multiple catalytic and regulatory subunits change their mRNA expression levels. In addition to the number of genes the fact that the alterations occur at multiple levels stresses the biological relevance of transcriptional regulation for adaptations of postsynaptic signaling pathways. The overall pattern of changes in both striatonigral and striatopallidal neurons is compatible with homeostatic mechanisms. In accordance with the distinct biological effects of dopamine D(1) and D(2) receptor stimulation, the alterations of the transcriptional profiles most likely result in prodopaminergic phosphorylation patterns. Our data provide insight into the disease-related plasticity of functional genomic networks in vivo that might contribute to the protracted preclinical phase of PD. In addition, the data have potential implications for the symptomatic treatment of the disease.

Indexed as

Adrenergic AgentsAnalysis of VarianceAnimalsCorpus StriatumDopamineDopamine AgentsDopamine and cAMP-Regulated Phosphoprotein 32Gene Expression ProfilingGene Expression RegulationIon ChannelsLevodopaMaleMicroarray AnalysisMicrodissectionNeural PathwaysNeuronsAdrenergic AgentsDopamineDopamine AgentsDopamine and cAMP-Regulated Phosphoprotein 32Ion ChannelsLevodopaOxidopamineWheat Germ Agglutinin-Horseradish Peroxidase Conjugate

Identifiers

PMID19474310
PMCPMC2758935
OpenAlexW1971035979

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.