Evidence map›Paper›PMID 11739600›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2001

cAMP response element-binding protein is required for dopamine-dependent gene expression in the intact but not the dopamine-denervated striatum.

M Andersson, C Konradi, M A Cenci

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

46 citing papers in PubMed, 144 citations in OpenAlex.

  1. Review
  2. BDNF/TrkB activators in Parkinson's disease: A new therapeutic strategy.Journal of cellular and molecular medicine · 2024
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  18. Striatal cholinergic cell ablation attenuates L-DOPA induced dyskinesia in Parkinsonian mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
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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 2 countries.

M AnderssonDepartment of Physiological Sciences, Neurobiology Division, Lund University, Wallenberg Neuroscience Centre, 221 84 Lund, Sweden.
C Konradi
M A Cenci
Lund University · SEHarvard University · US

Funding

PSYCHOSTIMULANT REGULATION OF NEURAL GENE EXPRESSIONR01DA007134 · NIDA · MC LEAN HOSPITAL (BELMONT, MA) · PI KONRADI, CHRISTINE L · 1991 to 2003
$1.1M
NIDA NIH HHS R01 DA007134
6 · The paper itself

Abstract

The cAMP response element-binding protein (CREB) is believed to play a pivotal role in dopamine (DA) receptor-mediated nuclear signaling and neuroplasticity. Here we demonstrate that the significance of CREB for gene expression depends on the experimental paradigm. We compared the role of CREB in two different but related models: l-DOPA administration to unilaterally 6-hydroxydopamine lesioned rats, and cocaine administration to neurologically intact animals. Antisense technology was used to produce a local knockdown of CREB in the lateral caudate-putamen, a region that mediates the dyskinetic or stereotypic manifestations associated with l-DOPA or cocaine treatment, respectively. In intact rats, CREB antisense reduced both basal and cocaine-induced expression of c-Fos, FosB/DeltaFosB, and prodynorphin mRNA. In the DA-denervated striatum, CREB was not required for l-DOPA to induce these gene products, nor did CREB contribute considerably to DNA binding activity at cAMP responsive elements (CREs) and CRE-like enhancers. DeltaFosB-related proteins and JunD were the main contributors to both CRE and AP-1 DNA-protein complexes in l-DOPA-treated animals. In behavioral studies, intrastriatal CREB knockdown caused enhanced activity scores in intact control animals and exacerbated the dyskinetic effects of acute l-DOPA treatment in 6-OHDA-lesioned animals. These data demonstrate that CREB is not required for the development of l-DOPA-induced dyskinesia in hemiparkinsonian rats. Moreover, our results reveal an unexpected alteration of nuclear signaling mechanisms in the parkinsonian striatum treated with l-DOPA, where AP-1 transcription factors appear to supersede CREB in the activation of CRE-containing genes.

Indexed as

AnimalsAntiparkinson AgentsCocaineCorpus StriatumCyclic AMP Response Element-Binding ProteinDenervationDNADopamineDopamine Uptake InhibitorsDose-Response Relationship, DrugDrug Administration RoutesEnkephalinsFemaleGene ExpressionLevodopaOligonucleotides, AntisenseAntiparkinson AgentsCocaineCyclic AMP Response Element-Binding ProteinDNADopamineDopamine Uptake InhibitorsEnkephalinsLevodopaOligonucleotides, AntisenseOxidopaminepreproenkephalinProtein PrecursorsProto-Oncogene Proteins c-fosRNA, MessengerTranscription Factor AP-1

Identifiers

PMID11739600
PMCPMC4204657
OpenAlexW2143656230

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.