Evidence map›Paper›PMID 24569009›Full record

ArticleBehavioural brain research2014

The role of the laterodorsal tegmental nucleus in methamphetamine conditioned place preference and locomotor activity.

Lauren K Dobbs, Christopher L Cunningham

Abstract read
In one paragraph

Article in Behavioural brain research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.0field-weighted citation impact, top 31% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Neurobiology of reward-related learning.Neuroscience and biobehavioral reviews · 2021
    Review
  8. Article
  9. Article
  10. Glucagon-Like Peptide-1 Receptor Signaling in the Lateral Dorsal Tegmental Nucleus Regulates Energy Balance.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018
    Article
  11. Article
  12. Structural and functional considerations of the cholinergic brainstem.Journal of neural transmission (Vienna, Austria : 1996) · 2016
    Review
  13. Review
  14. Review
  15. 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

2 authors at 1 institution in 1 country.

Lauren K DobbsDepartment of Behavioral Neuroscience, Oregon Health & Science University, 3181 SW Sam Jackson Park Rd, L470 , Portland, OR 97239, USA. Electronic address: Lauren.dobbs@nih.gov.
Christopher L CunninghamDepartment of Behavioral Neuroscience, Oregon Health & Science University, 3181 SW Sam Jackson Park Rd, L470 , Portland, OR 97239, USA.
Oregon Health & Science University · US

Funding

Translational measures of risk for excessive alcohol consumptionP60AA010760 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI Suzanne S. Fei · 2006 to 2026
$34.5M
BIOLOGICAL BASES OF DRUG-SEEKING BEHAVIORT32DA007262 · NIDA · OREGON HEALTH & SCIENCE UNIVERSITY · PI WILLIAMS, JOHN T · 1991 to 2022
$9.4M
MODULATION OF ALCOHOL REINFORCEMENTR01AA007702 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI RYABININ, ANDREY E · 1988 to 2019
$4.0M
Role of mesopontine cholinergic afferents in methamphetamine rewardF31DA027295 · NIDA · OREGON HEALTH & SCIENCE UNIVERSITY · PI DOBBS, LAUREN K · 2010 to 2011
$83k
NIAAA NIH HHS P60 AA010760NIAAA NIH HHS R01 AA007702NIAAA NIH HHS R01AA007702NIDA NIH HHS F31 DA027295NIDA NIH HHS F31DA027295NIDA NIH HHS T32 DA007262
6 · The paper itself

Abstract

Methamphetamine (METH) indirectly stimulates the laterodorsal tegmental nucleus (LDT) acetylcholine (ACh) neurons to increase ACh within the ventral tegmental area (VTA). LDT ACh inhibition attenuates METH and saline locomotor activity. The aim of these experiments was to determine whether LDT ACh contributes to METH conditioned place preference (CPP). C57BL/6J mice received a bilateral electrolytic or sham lesion of the LDT. After recovery, mice received alternating pairings of METH (0.5 mg/kg) and saline with distinct tactile floor cues over 8 days. During preference tests, mice were given access to both floor types and time spent on each was recorded. Mice were tested again after exposure to both extinction and reconditioning trials. Brains were then processed for choline acetyltransferase immunohistochemistry to label LDT ACh neurons. Lesioned mice had significantly fewer LDT ACh neurons and showed increased saline and METH locomotor activity during the first conditioning trial compared to sham mice. Locomotor activity (saline and METH) was negatively correlated with the number of LDT ACh neurons. Lesioned and sham mice showed similar METH CPP following conditioning, extinction and reconditioning trials. LDT ACh neurons are not necessary for METH reward as indexed by CPP, but may be important for basal and METH-induced locomotor activity.

Indexed as

Analysis of VarianceAnimalsCholine O-AcetyltransferaseConditioning, OperantDopamine Uptake InhibitorsElectrolysisExtinction, PsychologicalMaleMethamphetamineMiceMice, Inbred C57BLMorphineMotor ActivityNarcoticsTegmentum MesencephaliCholine O-AcetyltransferaseDopamine Uptake InhibitorsMethamphetamineMorphineNarcoticsAcetylcholineElectrolytic lesionInbred mice (C57BL/6)Locomotor activityMethamphetamineReward

Identifiers

PMID24569009
PMCPMC4020626
OpenAlexW2022401043

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.