Evidence map›Paper›PMID 23551948›Full record

ArticleThe Journal of physiology2013

Striatal neurones have a specific ability to respond to phasic dopamine release.

Liliana R V Castro, Marina Brito, Elvire Guiot, Marina Polito, Christoph W Korn, Denis Hervé, Jean-Antoine Girault, Danièle Paupardin-Tritsch, Pierre Vincent

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 7% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 64 citations in OpenAlex.

  1. The Signaling and Pharmacology of the Dopamine D1 Receptor.Frontiers in cellular neuroscience · 2021
    Pooled it
  2. Review
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  8. Review
  9. Neuromodulation of Astrocytic KInternational journal of molecular sciences · 2021
    Article
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  15. Protocol for Isolating the Mouse Circle of Willis.Journal of visualized experiments : JoVE · 2016
    Article
  16. Article
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  19. Article
  20. Can intracellular cAMP dynamics enable scalable computation?Frontiers in cellular neuroscience · 2015
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 2 countries.

Liliana R V CastroNeurobiologie des Processus Adaptatifs UMR7102 CNRS UPMC, F-75005 Paris, France.
Marina Brito
Elvire Guiot
Marina Polito
Christoph W Korn
Denis Hervé
Jean-Antoine Girault
Danièle Paupardin-Tritsch
Pierre Vincent
Centre National de la Recherche Scientifique · FRSorbonne Université · FRInserm · FRUniversity of Coimbra · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cAMP/protein kinase A (PKA) signalling cascade is ubiquitous, and each step in this cascade involves enzymes that are expressed in multiple isoforms. We investigated the effects of this diversity on the integration of the pathway in the target cell by comparing prefrontal cortical neurones with striatal neurones which express a very specific set of signalling proteins. The prefrontal cortex and striatum both receive dopaminergic inputs and we analysed the dynamics of the cAMP/PKA signal triggered by dopamine D1 receptors in these two brain structures. Biosensor imaging in mouse brain slice preparations showed profound differences in the D1 response between pyramidal cortical neurones and striatal medium spiny neurones: the cAMP/PKA response was much stronger, faster and longer lasting in striatal neurones than in pyramidal cortical neurones. We identified three molecular determinants underlying these differences: different activities of phosphodiesterases, particularly those of type 4, which strongly damp the cAMP signal in the cortex but not in the striatum; stronger adenylyl cyclase activity in the striatum, generating responses with a faster onset than in the cortex; and DARPP-32, a phosphatase inhibitor which prolongs PKA action in the striatum. Striatal neurones were also highly responsive in terms of gene expression since a single sub-second dopamine stimulation is sufficient to trigger c-Fos expression in the striatum, but not in the cortex. Our data show how specific molecular elements of the cAMP/PKA signalling cascade selectively enable the principal striatal neurones to respond to brief dopamine stimuli, a critical process in incentive learning.

Indexed as

1-Methyl-3-isobutylxanthine2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepineAnimalsBiosensing TechniquesColforsinCorpus StriatumCyclic AMPCyclic AMP-Dependent Protein KinasesCyclic Nucleotide Phosphodiesterases, Type 4DopamineDopamine AgonistsDopamine and cAMP-Regulated Phosphoprotein 32In Vitro TechniquesMaleMiceMice, Inbred C57BL1-Methyl-3-isobutylxanthine2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepineColforsinCyclic AMPCyclic AMP-Dependent Protein KinasesCyclic Nucleotide Phosphodiesterases, Type 4DopamineDopamine AgonistsDopamine and cAMP-Regulated Phosphoprotein 32Phosphodiesterase InhibitorsPpp1r1b protein, mouseProto-Oncogene Proteins c-fos

Identifiers

PMID23551948
PMCPMC3717223
OpenAlexW2107239850

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.