Evidence map›Paper›PMID 28243713›Full record

ArticlePsychopharmacology2017

mPer1 promotes morphine-induced locomotor sensitization and conditioned place preference via histone deacetylase activity.

Stéphanie Perreau-Lenz, Laura-Sophie Hoelters, Sarah Leixner, Carla Sanchis-Segura, Anita Hansson, Ainhoa Bilbao, Rainer Spanagel

Abstract read
PubMed Publisher
In one paragraph

Article in Psychopharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.4field-weighted citation impact, top 48% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. The Brain's Reward System in Health and Disease.Advances in experimental medicine and biology · 2021
    Article
  11. Article
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

7 authors at 4 institutions in 2 countries.

Stéphanie Perreau-LenzCentral Institute for Mental Health, Institute of Psychopharmacology, Medical Faculty Mannheim, University of Heidelberg, Heidelberg, Germany. stephanie.perreau-lenz@sri.com.
Laura-Sophie HoeltersCentral Institute for Mental Health, Institute of Psychopharmacology, Medical Faculty Mannheim, University of Heidelberg, Heidelberg, Germany.
Sarah LeixnerCentral Institute for Mental Health, Institute of Psychopharmacology, Medical Faculty Mannheim, University of Heidelberg, Heidelberg, Germany.
Carla Sanchis-SeguraArea de Psicobiologia, Universitat Jaume I, Castelló, Spain.
Anita HanssonCentral Institute for Mental Health, Institute of Psychopharmacology, Medical Faculty Mannheim, University of Heidelberg, Heidelberg, Germany.
Ainhoa BilbaoCentral Institute for Mental Health, Institute of Psychopharmacology, Medical Faculty Mannheim, University of Heidelberg, Heidelberg, Germany.
Rainer SpanagelCentral Institute for Mental Health, Institute of Psychopharmacology, Medical Faculty Mannheim, University of Heidelberg, Heidelberg, Germany.
Heidelberg University · DECentral Institute of Mental Health · DEUniversitat Jaume I · ESUniversity Hospital Heidelberg · DE

Funding

Casein Kinase 1, Alcohol Abuse and Comorbid Sleep and Circadian DisturbancesR21AA023078 · NIAAA · SRI INTERNATIONAL · PI PERREAU-LENZ, STEPHANIE · 2014 to 2015
$486k
NIAAA NIH HHS R21 AA023078
6 · The paper itself

Abstract

rationalePrevious studies have shown that repeated exposure to drugs of abuse is associated with changes in clock genes expression and that mice strains with various mutations in clock genes show alterations in drug-induced behaviors.

objectiveThe objective of this study is to characterize the role of the clock gene mPer1 in the development of morphine-induced behaviors and a possible link to histone deacetylase (HDAC) activity.

methodsIn Per1

resultsPer1

conclusionsOur results reveal that although the mPer1 gene does not alter morphine-induced antinociception nor withdrawal, it plays a prominent role in the development of morphine-induced behavioral sensitization and reward via inhibitory modulation of striatal HDAC activity. These data suggest that PER1 inhibits deacetylation to promote drug-induced neuroplastic changes.

Indexed as

Analgesics, OpioidAnimalsConditioning, PsychologicalCorpus StriatumDrug ToleranceEnzyme ActivationHistone Deacetylase InhibitorsHistone DeacetylasesLocomotionMaleMiceMice, KnockoutMice, TransgenicMorphineNaloxonePeriod Circadian ProteinsAnalgesics, OpioidHistone Deacetylase InhibitorsHistone DeacetylasesMorphineNaloxonePer1 protein, mousePeriod Circadian ProteinsAddictionBehavioral sensitizationClock genesCPPEpigeneticHDACMiceOpioidsPer1Sodium butyrate

Identifiers

PMID28243713
OpenAlexW2594833403

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.