Evidence map›Paper›PMID 28547130›Full record

ArticlePsychopharmacology2017

Extracellular dopamine, acetylcholine, and activation of dopamine D1 and D2 receptors after selective breeding for cocaine self-administration in rats.

Haiyang Xu, Sasmita Das, Marc Sturgill, Colin Hodgkinson, Qiaoping Yuan, David Goldman, Kenneth Grasing

Open access · greenAbstract read
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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 47% 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

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. 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 1 country.

Haiyang XuSubstance Abuse Research Laboratory, 151, Kansas City Veterans Affairs Medical Center, 4801 Linwood Boulevard, Kansas City, MO, 64128, USA.
Sasmita DasMolecular Bio-Nanotechnology, Imaging and Therapeutic Research Unit, 151, Kansas City Veterans Affairs Medical Center, 4801 Linwood Boulevard, Kansas City, MO, 64128, USA.
Marc SturgillDepartment of Pharmacy Practice and Administration, Ernest Mario School of Pharmacy, Rutgers, the State University of New Jersey, Piscataway, NJ, 08854, USA.
Colin HodgkinsonLaboratory of Neurogenetics, National Institute on Alcohol Abuse and Alcoholism, 9000 Rockville Pike, Bethesda, MD, 20852, USA.
Qiaoping YuanLaboratory of Neurogenetics, National Institute on Alcohol Abuse and Alcoholism, 9000 Rockville Pike, Bethesda, MD, 20852, USA.
David GoldmanLaboratory of Neurogenetics, National Institute on Alcohol Abuse and Alcoholism, 9000 Rockville Pike, Bethesda, MD, 20852, USA.
Kenneth GrasingSubstance Abuse Research Laboratory, 151, Kansas City Veterans Affairs Medical Center, 4801 Linwood Boulevard, Kansas City, MO, 64128, USA. kgrasing@kumc.edu.
National Institute on Alcohol Abuse and Alcoholism · USRutgers, The State University of New Jersey · USUniversity of Kansas · USUniversity of Kansas Medical Center · US

Funding

Integrative genetics of behavior with high throughput technologiesZIAAA000301 · NIAAA · NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM · PI GOLDMAN, DAVID · 2009 to 2025
$68.6M
Tacrine Effects on Cocaine Self-Administration and Pharmacokinetic MeasuresR21DA029787 · NIDA · MIDWEST VETERANS' BIOMEDICAL RESEARCH FOUNDATION · PI GRASING, KENNETH W. · 2011 to 2012
$351k
Lorcaserin Effects on Cocaine Craving and Drug-Reinforced BehaviorR21DA037556 · NIDA · MIDWEST VETERANS' BIOMEDICAL RESEARCH FOUNDATION · PI GRASING, KENNETH W. · 2014 to 2017
$344k
Persistent Attenuation of Cocaine-Reinforced BehaviorI01BX000958 · VA · KANSAS CITY VA MEDICAL CENTER · PI GRASING, KENNETH W. · 2012 to 2015
–
BLRD VA I01 BX000958NIDA NIH HHS R21 DA029787NIDA NIH HHS R21 DA037556
6 · The paper itself

Abstract

rationaleThe low self-administration (LS)/Kgras (LS) and high self-administration (HS)/Kgras (HS) rat lines were generated by selective breeding for low- and high-intravenous cocaine self-administration, respectively, from a common outbred Wistar stock (Crl:WI). This trait has remained stable after 13 generations of breeding.

objectiveThe objective of the present study is to compare cocaine preference, neurotransmitter release, and dopamine receptor activation in LS and HS rats.

methodsLevels of dopamine, acetylcholine, and cocaine were measured in the nucleus accumbens (NA) shell of HS and LS rats by tandem mass spectrometry of microdialysates. Cocaine-induced locomotor activity and conditioned-place preference were compared between LS and HS rats.

resultsHS rats displayed greater conditioned-place preference scores compared to LS and reduced basal extracellular concentrations of dopamine and acetylcholine. However, patterns of neurotransmitter release did not differ between strains. Low-dose cocaine increased locomotor activity in LS rats, but not in HS animals, while high-dose cocaine augmented activity only in HS rats. Either dose of cocaine increased immunoreactivity for c-Fos in the NA shell of both strains, with greater elevations observed in HS rats. Activation identified by cells expressing both c-Fos and dopamine receptors was generally greater in the HS strain, with a similar pattern for both D1 and D2 dopamine receptors.

conclusionsDiminished levels of dopamine and acetylcholine in the NA shell, with enhanced cocaine-induced expression of D1 and D2 receptors, are associated with greater rewarding effects of cocaine in HS rats and an altered dose-effect relationship for cocaine-induced locomotor activity.

Indexed as

AcetylcholineAnimalsCocaineDopamineDopamine Uptake InhibitorsMaleMotor ActivityNucleus AccumbensRatsReceptors, Dopamine D1Receptors, Dopamine D2Selective BreedingSelf AdministrationAcetylcholineCocaineDopamineDopamine Uptake InhibitorsReceptors, Dopamine D1Receptors, Dopamine D2Conditioned-place preferenceDopamine D1 receptorDopamine D2 receptorNucleus accumbens shellRewardSelective breedingSelf-administration

Identifiers

PMID28547130
PMCPMC5538921
OpenAlexW2617782379

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.