Evidence map›Paper›PMID 30803445›Full record

ArticleMolecular brain2019

Neuronal scaffolding protein spinophilin is integral for cocaine-induced behavioral sensitization and ERK1/2 activation.

Lorena Bianchine Areal, Alison Hamilton, Cristina Martins-Silva, Rita Gomes Wanderley Pires, Stephen S G Ferguson

Open access · goldAbstract read
In one paragraph

Article in Molecular brain, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.4field-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

19 citing papers in PubMed, 29 citations in OpenAlex.

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  12. Serine Racemase Expression by Striatal Neurons.Cellular and molecular neurobiology · 2022
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  15. Modulation of dendritic spines by protein phosphatase-1.Advances in pharmacology (San Diego, Calif.) · 2021
    Review
  16. Review
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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

5 authors at 3 institutions in 3 countries.

Lorena Bianchine ArealDepartment of Cellular and Molecular Medicine and University of Ottawa Brain and Mind Institute, University of Ottawa, 451 Smyth Road, Ottawa, ON, K1H 8M5, Canada.
Alison HamiltonDepartment of Cellular and Molecular Medicine and University of Ottawa Brain and Mind Institute, University of Ottawa, 451 Smyth Road, Ottawa, ON, K1H 8M5, Canada.
Cristina Martins-SilvaDepartment of Physiological Sciences, Health Sciences Center, Federal University of Espirito, Santo, Vitoria, ES, 29043-910, Brazil.
Rita Gomes Wanderley PiresGraduate Program in Neuroscience, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, MG, 31270-901, Brazil.
Stephen S G FergusonDepartment of Cellular and Molecular Medicine and University of Ottawa Brain and Mind Institute, University of Ottawa, 451 Smyth Road, Ottawa, ON, K1H 8M5, Canada. sferguso@uottawa.ca.ORCID 0000-0002-0887-7312
Universidade Federal de Minas Gerais · BRUniversity of Ottawa · CAUniversidade Federal do Espírito Santo · BR

Funding

CIHR MOP 119437
6 · The paper itself

Abstract

Spinophilin is a scaffolding protein enriched in dendritic spines with integral roles in the regulation of spine density and morphology, and the modulation of synaptic plasticity. The ability of spinophilin to alter synaptic strength appears to involve its scaffolding of key synaptic proteins, including the important structural element F-actin, AMPA/NMDA modulator protein phosphatase 1, and neuromodulatory G-protein coupled receptors, including dopamine receptor D2 and metabotropic glutamate receptor 5. Additionally, spinophilin is highly expressed in the striatum, a brain region that is fundamentally involved in reward-processing and locomotor activity which receives both glutamatergic and dopaminergic inputs. Therefore, we aimed to investigate the role of spinophilin in behavioral responses to cocaine, evaluating wild-type and spinophilin knockout mice followed by the examination of underlying molecular alterations. Although acute locomotor response was not affected, deletion of spinophilin blocked the development and expression of behavioral sensitization to cocaine while maintaining normal conditioned place preference. This behavioral alteration in spinophilin knockout mice was accompanied by attenuated c-Fos and ∆FosB expression following cocaine administration and blunted cocaine-induced phosphorylation of ERK1/2 in the striatum, with no change in other relevant signaling molecules. Therefore, we suggest spinophilin fulfills an essential role in cocaine-induced behavioral sensitization, likely via ERK1/2 phosphorylation and induction of c-Fos and ∆FosB in the striatum, a mechanism that may underlie specific processes in cocaine addiction.

Indexed as

AnimalsBehavior, AnimalChoice BehaviorCocaineCorpus StriatumEnzyme ActivationExtracellular Signal-Regulated MAP KinasesGene DeletionGene Expression RegulationImidazolesMice, Inbred C57BLMice, KnockoutMicrofilament ProteinsMotor ActivityNerve Tissue ProteinsNeurabins2-chloro-4-((2,5-dimethyl-1-(4-(trifluoromethoxy)phenyl)-1H-imidazol-4-yl)ethynyl)pyridineCocaineExtracellular Signal-Regulated MAP Kinasesglutamine receptorImidazolesMicrofilament ProteinsNerve Tissue ProteinsNeurabinsNR2A NMDA receptorProto-Oncogene Proteins c-fosPyridinesReceptor, Metabotropic Glutamate 5Receptors, DopamineReceptors, NeurotransmitterReceptors, N-Methyl-D-AspartateBehavioral sensitizationCocaineDrug addictionSpinophilin

Identifiers

PMID30803445
PMCPMC6388481
OpenAlexW2930990488

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.