Evidence map›Paper›PMID 24725970›Full record

ArticleBiological psychiatry2014

Cell-type specific expression of p11 controls cocaine reward.

Margarita Arango-Lievano, Justin T Schwarz, Mary Vernov, Matthew B Wilkinson, Kathryn Bradbury, Akira Feliz, Roberta Marongiu, Yaroslav Gelfand, Jennifer Warner-Schmidt, Eric J Nestler and 3 more

Abstract read
In one paragraph

Article in Biological psychiatry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Inducible CRISPR Epigenome Systems Mimic Cocaine Induced Bidirectional Regulation of Nab2 and Egr3.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Journal of psychiatry & neuroscience : JPN · 2017
    Article
  9. Article
  10. Gene therapy blockade of dorsal striatal p11 improves motor function and dyskinesia in parkinsonian mice.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  11. Opposing role for Egr3 in nucleus accumbens cell subtypes in cocaine action.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 1 country.

Margarita Arango-LievanoLaboratory of Molecular Neurosurgery, Department of Neurological Surgery, Weill Cornell Medical College, New York, New York.
Justin T SchwarzLaboratory of Molecular Neurosurgery, Department of Neurological Surgery, Weill Cornell Medical College, New York, New York.
Mary VernovLaboratory of Molecular Neurosurgery, Department of Neurological Surgery, Weill Cornell Medical College, New York, New York.
Matthew B WilkinsonFishberg Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
Kathryn BradburyFishberg Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
Akira FelizLaboratory of Molecular Neurosurgery, Department of Neurological Surgery, Weill Cornell Medical College, New York, New York.
Roberta MarongiuLaboratory of Molecular Neurosurgery, Department of Neurological Surgery, Weill Cornell Medical College, New York, New York.
Yaroslav GelfandLaboratory of Molecular Neurosurgery, Department of Neurological Surgery, Weill Cornell Medical College, New York, New York.
Jennifer Warner-SchmidtLaboratory of Molecular and Cellular Neuroscience, Rockefeller University, New York, New York.
Eric J NestlerFishberg Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York; Psychiatry and Pharmacology, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
Paul GreengardLaboratory of Molecular and Cellular Neuroscience, Rockefeller University, New York, New York.
Scott J RussoFishberg Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
Michael G KaplittFishberg Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York. Electronic address: mik2002@med.cornell.edu.
Neurological Surgery · USIcahn School of Medicine at Mount Sinai · USAllen Institute for Brain Science · USCornell University · USRockefeller University · US

Funding

TRANSGENIC COREP01DA008227 · NIDA · YALE UNIVERSITY · PI NESTLER, ERIC J. · 1993 to 2018
$28.1M
THE ROLE OF DARPPS IN THE ACUTE AND CHRONIC EFFECTS OF COCAINE AND AMPHETAMINEP01DA010044 · NIDA · ROCKEFELLER UNIVERSITY · PI GREENGARD, PAUL · 1996 to 2015
$23.6M
NIDA NIH HHS P01 DA008227NIDA NIH HHS P01 DA010044
6 · The paper itself

Abstract

backgroundThe high rate of comorbidity between depression and cocaine addiction suggests shared molecular mechanisms and anatomical pathways. Limbic structures, such as the nucleus accumbens (NAc), play a crucial role in both disorders, yet how different cell types within these structures contribute to the pathogenesis remains elusive. Downregulation of p11 (S100A10), specifically in the NAc, elicits depressive-like behaviors in mice, but its role in drug addiction is unknown.

methodsWe combined mouse genetics and viral strategies to determine how the titration of p11 levels within the entire NAc affects the rewarding actions of cocaine on behavior (six to eight mice per group) and molecular correlates (three experiments, five to eight mice per group). Finally, the manipulation of p11 expression in distinct NAc dopaminoceptive neuronal subsets distinguished cell-type specific effects of p11 on cocaine reward (five to eight mice per group).

resultsWe demonstrated that p11 knockout mice have enhanced cocaine conditioned place preference, which is reproduced by the focal downregulation of p11 in the NAc of wild-type mice. In wild-type mice, cocaine reduced p11 expression in the NAc, while p11 overexpression exclusively in the NAc reduced cocaine conditioned place preference. Finally, we identified dopamine receptor-1 expressing medium spiny neurons as key mediators of the effects of p11 on cocaine reward.

conclusionsOur data provide evidence that disruption of p11 homeostasis in the NAc, particularly in dopamine receptor-1 expressing medium spiny neurons, may underlie pathophysiological mechanisms of cocaine rewarding action. Treatments to counter maladaptation of p11 levels may provide novel therapeutic opportunities for cocaine addiction.

Indexed as

RewardAnimalsAnnexin A2CocaineConditioning, PsychologicalDown-RegulationMaleMiceMice, Inbred C57BLMotor ActivityNeuronsNucleus AccumbensReceptors, Dopamine D1S100 Calcium Binding Protein A10S100 ProteinsAnnexin A2CocaineReceptors, Dopamine D1S100 Calcium Binding Protein A10S100 ProteinsCocaine rewardconditional knock downnucleus accumbensp11 (s100a10)striatonigral pathwaystriatopallidal pathway

Identifiers

PMID24725970
PMCPMC4145045
OpenAlexW1989550232

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.