Evidence map›Paper›PMID 24813704›Full record

ArticlePhysiology & behavior2014

Genetic deletion of the MT1 or MT2 melatonin receptors abrogates methamphetamine-induced reward in C3H/HeN mice.

Shannon J Clough, Anthony J Hutchinson, Randall L Hudson, Margarita L Dubocovich

Open access · greenAbstract read
In one paragraph

Article in Physiology & behavior, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.8field-weighted citation impact, top 35% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Adrenal MTHormones and behavior · 2022
    Article
  2. Article
  3. Article
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  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Learned motivation drives circadian physiology in the absence of the master circadian clock.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2017
    Article
  12. Update on melatonin receptors: IUPHAR Review 20.British journal of pharmacology · 2016
    Review
  13. MT1 and MT2 Melatonin Receptors: A Therapeutic Perspective.Annual review of pharmacology and toxicology · 2016
    Review
  14. 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

4 authors at 1 institution in 1 country.

Shannon J CloughDepartment of Pharmacology & Toxicology, School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY 14214, United States.
Anthony J HutchinsonDepartment of Pharmacology & Toxicology, School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY 14214, United States.
Randall L HudsonDepartment of Physiology and Biophysics, School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY 14214, United States.
Margarita L DubocovichDepartment of Pharmacology & Toxicology, School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY 14214, United States. Electronic address: mdubo@buffalo.edu.
University at Buffalo, State University of New York · US

Funding

Modulation of Methamphetamine Actions in the CNSR01DA021870 · NIDA · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI DUBOCOVICH, MARGARITA L · 2007 to 2011
$1.6M
NIDA NIH HHS DA 021870NIDA NIH HHS R01 DA021870
6 · The paper itself

Abstract

The drug of abuse methamphetamine (METH) is known for its ability to enhance reward responses. The rewarding properties of psychostimulants have been shown to vary across time of day in mice. The goal of this study was to determine the role of the MT1 and MT2 melatonin receptors in METH-induced reward, as measured by the conditioned place preference (CPP) paradigm during the light and dark phases. C3H/HeN wild-type mice were trained for METH-induced CPP at either ZT 6-8 (ZT: Zeitgeber time; ZT 0=lights on), when endogenous melatonin levels are low, or ZT 19-21, when melatonin levels are high. These time points also correspond to the high and low points for expression of the circadian gene Period1, respectively. The locomotor response to METH (1.2mg/kg, ip) treatment was of similar magnitude at both times; however only C3H/HeN mice conditioned to METH at ZT 6-8 developed a place preference. C3H/HeN mice with a genetic deletion of either the MT1 (MT1KO) or MT2 (MT2KO) receptor tested at ZT 6-8 or ZT 19-21 did not develop a place preference for METH, though both showed a similar increase in locomotor activity following METH treatment when compared to wild-type mice. We conclude that in our mouse model METH-induced CPP is dependent on time of day and the presence of the MT1 or MT2 receptors, suggesting a role for melatonin in METH-induced reward.

Indexed as

RewardAnalysis of VarianceAnimalsCentral Nervous System StimulantsConditioning, OperantDose-Response Relationship, DrugLocomotionMaleMelatoninMethamphetamineMiceMice, Inbred C3HMice, KnockoutReceptor, Melatonin, MT1Receptor, Melatonin, MT2Time FactorsCentral Nervous System StimulantsMelatoninMethamphetamineReceptor, Melatonin, MT1Receptor, Melatonin, MT2C3H/HeN mouseConditioned place preferenceMelatoninMelatonin receptorsMT(1) or MT(2) knockout mice

Identifiers

PMID24813704
PMCPMC4698795
OpenAlexW2005367665

What OpenQuestion holds

Textmetadata
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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.