Evidence map›Paper›PMID 28044061›Full record

ArticleMolecular psychiatry2018

In silico identification and in vivo validation of miR-495 as a novel regulator of motivation for cocaine that targets multiple addiction-related networks in the nucleus accumbens.

R M Bastle, R J Oliver, A S Gardiner, N S Pentkowski, F Bolognani, A M Allan, T Chaudhury, M St Peter, N Galles, C Smith and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular psychiatry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 3 pooled it
1.8field-weighted citation impact, top 17% 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

43 citing papers in PubMed, 3 syntheses or guidelines pooled it, 61 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Role of microRNAs in the pathophysiology of addiction.Wiley interdisciplinary reviews. RNA · 2021
    Pooled it
  4. Review
  5. Article
  6. Multi-omics Analysis Reveals miR-7220-5p Alleviates NThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Frontiers in oncology · 2023
    Article
  17. Epigenetic Modulation of Opioid Receptors by Drugs of Abuse.International journal of molecular sciences · 2022
    Review
  18. Review
  19. Article
  20. Review
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

12 authors at 2 institutions in 1 country.

R M BastleSchool of Life Sciences, Arizona State University, Tempe, AZ, USA.
R J OliverDepartment of Neurosciences, University of New Mexico School of Medicine, Albuquerque, NM, USA.
A S GardinerDepartment of Neurosciences, University of New Mexico School of Medicine, Albuquerque, NM, USA.
N S PentkowskiSchool of Life Sciences, Arizona State University, Tempe, AZ, USA.
F BolognaniDepartment of Neurosciences, University of New Mexico School of Medicine, Albuquerque, NM, USA.
A M AllanDepartment of Neurosciences, University of New Mexico School of Medicine, Albuquerque, NM, USA.
T ChaudhurySchool of Life Sciences, Arizona State University, Tempe, AZ, USA.
M St PeterSchool of Life Sciences, Arizona State University, Tempe, AZ, USA.
N GallesSchool of Life Sciences, Arizona State University, Tempe, AZ, USA.
C SmithSchool of Life Sciences, Arizona State University, Tempe, AZ, USA.
J L NeisewanderSchool of Life Sciences, Arizona State University, Tempe, AZ, USA.
N I Perrone-BizzozeroDepartment of Neurosciences, University of New Mexico School of Medicine, Albuquerque, NM, USA.
Arizona State University · USUniversity of New Mexico · US

Funding

Alcohol Research Training in NeurosciencesT32AA014127 · NIAAA · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Jonathan L Brigman · 2003 to 2026
$3.3M
Competing roles of microRNAs and RNA-binding proteins in drug addictionR01DA034097 · NIDA · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI NEISEWANDER, JANET L, PERRONE-BIZZOZERO, NORA IRMA · 2012 to 2016
$2.2M
Impact of miR-495 vs. HuD in the Control of Addiction-Related Genes and BehaviorR21DA034452 · NIDA · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI PERRONE-BIZZOZERO, NORA IRMA · 2012 to 2013
$370k
Role of MicroRNAs and RNA-Binding Proteins in Addiction-Related Gene ExpressionR03DA025992 · NIDA · UNIVERSITY OF NEW MEXICO · PI PERRONE-BIZZOZERO, NORA IRMA · 2008 to 2009
$316k
MicroRNA regulation of addiction-related genes and drug abuse-related behaviorF31DA035069 · NIDA · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI BASTLE, RYAN · 2013 to 2015
$125k
Opposing roles of miR-495 and HuD in addiction-related plasticity and behaviorF31DA041214 · NIDA · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI OLIVER, ROBERT JOHN · 2016 to 2017
$54k
NIAAA NIH HHS T32 AA014127NIDA NIH HHS F31 DA035069NIDA NIH HHS F31 DA041214NIDA NIH HHS R01 DA034097NIDA NIH HHS R03 DA025992NIDA NIH HHS R21 DA034452
6 · The paper itself

Abstract

MicroRNAs (miRNAs) are important post-transcriptional regulators of gene expression and are implicated in the etiology of several neuropsychiatric disorders, including substance use disorders (SUDs). Using in silico genome-wide sequence analyses, we identified miR-495 as a miRNA whose predicted targets are significantly enriched in the Knowledgebase for Addiction Related Genes (ARG) database (KARG; http://karg.cbi.pku.edu.cn). This small non-coding RNA is also highly expressed within the nucleus accumbens (NAc), a pivotal brain region underlying reward and motivation. Using luciferase reporter assays, we found that miR-495 directly targeted the 3'UTRs of Bdnf, Camk2a and Arc. Furthermore, we measured miR-495 expression in response to acute cocaine in mice and found that it is downregulated rapidly and selectively in the NAc, along with concomitant increases in ARG expression. Lentiviral-mediated miR-495 overexpression in the NAc shell (NAcsh) not only reversed these cocaine-induced effects but also downregulated multiple ARG mRNAs in specific SUD-related biological pathways, including those that regulate synaptic plasticity. miR-495 expression was also downregulated in the NAcsh of rats following cocaine self-administration. Most importantly, we found that NAcsh miR-495 overexpression suppressed the motivation to self-administer and seek cocaine across progressive ratio, extinction and reinstatement testing, but had no effect on food reinforcement, suggesting that miR-495 selectively affects addiction-related behaviors. Overall, our in silico search for post-transcriptional regulators identified miR-495 as a novel regulator of multiple ARGs that have a role in modulating motivation for cocaine.

Indexed as

3' Untranslated RegionsAnimalsBehavior, AddictiveCocaineCocaine-Related DisordersComputer SimulationConditioning, OperantExtinction, PsychologicalGene ExpressionGene Expression RegulationHumansMaleMiceMice, Inbred C57BLMicroRNAsMotivation3' Untranslated RegionsCocaineMicroRNAsMIRN495 microRNA, humanMIRN495 microRNA, mouse

Identifiers

PMID28044061
PMCPMC5495632
OpenAlexW2564063960

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.