Evidence map›Paper›PMID 22672659›Full record

ArticleJournal of pineal research2012

Genetic deletion of MT(1) and MT(2) melatonin receptors differentially abrogates the development and expression of methamphetamine-induced locomotor sensitization during the day and the night in C3H/HeN mice.

Anthony J Hutchinson, Randall L Hudson, Margarita L Dubocovich

Abstract read
In one paragraph

Article in Journal of pineal research, 2012. 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
1.1field-weighted citation impact, top 29% 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, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Pharmacological Actions of Carbamate Insecticides at Mammalian Melatonin Receptors.The Journal of pharmacology and experimental therapeutics · 2021
    Article
  4. Review
  5. Article
  6. 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
  7. Update on melatonin receptors: IUPHAR Review 20.British journal of pharmacology · 2016
    Review
  8. MT1 and MT2 Melatonin Receptors: A Therapeutic Perspective.Annual review of pharmacology and toxicology · 2016
    Review
  9. Review
  10. 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

3 authors at 1 institution in 1 country.

Anthony J HutchinsonDepartment of Pharmacology and Toxicology, School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY 14221, USA.
Randall L Hudson
Margarita L Dubocovich
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 R01 DA021870NIDA NIH HHS R01DA021870
6 · The paper itself

Abstract

This study explored the role of the melatonin receptors in methamphetamine (METH)-induced locomotor sensitization during the light and dark phases in C3H/HeN mice with genetic deletion of the MT(1) and/or MT(2) melatonin receptors. Six daily treatments with METH (1.2 mg/kg, i.p.) in a novel environment during the light phase led to the development of locomotor sensitization in wild-type (WT), MT(1)KO and MT(2)KO mice. Following four full days of abstinence, METH challenge (1.2 mg/kg, i.p.) triggered the expression of locomotor sensitization in METH-pretreated but not in vehicle (VEH)-pretreated mice. In MT(1)/MT(2)KO mice, the development of sensitization during the light phase was significantly reduced and the expression of sensitization was completely abrogated upon METH challenge. During the dark phase the development of locomotor sensitization in METH-pretreated WT, MT(1)KO and MT(2)KO mice was statistically different from VEH-treated controls. However, WT and MT(2)KO, but not MT(1)KO mice receiving repeated VEH pretreatments during the dark phase expressed a sensitized response to METH challenge that is of an identical magnitude to that observed upon 6 days of METH pretreatment. We conclude that exposure to a novel environment during the dark phase, but not during the light phase, facilitated the expression of sensitization to a METH challenge in a manner dependent on MT(1) melatonin receptor activation by endogenous melatonin. We suggest that MT(1) and MT(2) melatonin receptors are potential targets for pharmacotherapeutic intervention in METH abusers.

Indexed as

Gene DeletionPhotoperiodAnimalsBehavior, AnimalCentral Nervous SystemCentral Nervous System SensitizationCentral Nervous System StimulantsMaleMelatoninMethamphetamineMiceMice, Inbred C3HMice, KnockoutMotor ActivityReceptor, Melatonin, MT1Receptor, Melatonin, MT2Central Nervous System StimulantsMelatoninMethamphetamineReceptor, Melatonin, MT1Receptor, Melatonin, MT2

Identifiers

PMID22672659
PMCPMC3568497
OpenAlexW1933917044

What OpenQuestion holds

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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.