Evidence map›Paper›PMID 30191259›Full record

ArticlePsychopharmacology2019

Analysis of neurotransmitter levels in addiction-related brain regions during synthetic cathinone self-administration in male Sprague-Dawley rats.

Julie A Marusich, Elaine A Gay, Bruce E Blough

Erratum issuedAbstract read
In one paragraph

Article in Psychopharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

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  8. Neurotransmitter system aberrations in patients with drug addiction.Journal of neural transmission (Vienna, Austria : 1996) · 2020
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Julie A MarusichCenter for Drug Discovery, RTI International, 3040 Cornwallis Rd, 136 Hermann, Research Triangle Park, NC, 27709, USA. jmarusich@rti.org.ORCID http://orcid.org/0000-0002-0203-4867
Elaine A GayCenter for Drug Discovery, RTI International, 3040 Cornwallis Rd, 136 Hermann, Research Triangle Park, NC, 27709, USA.
Bruce E BloughCenter for Drug Discovery, RTI International, 3040 Cornwallis Rd, 136 Hermann, Research Triangle Park, NC, 27709, USA.
RTI International · US

Funding

POTENTIAL TREATMENT MEDICATIONS FOR DRUG ABUSER01DA012970 · NIDA · RESEARCH TRIANGLE INSTITUTE · PI BLOUGH, BRUCE E · 1999 to 2013
$5.5M
Neurochemical and Inflammatory Dysregulation During Synthetic Cathinone Self-AdministrationR21DA039315 · NIDA · RESEARCH TRIANGLE INSTITUTE · PI MARUSICH, JULIE A · 2017 to 2018
$527k
National Institute on Drug Abuse DA012970National Institute on Drug Abuse DA039315NIDA NIH HHS R01 DA012970NIDA NIH HHS R21 DA039315
6 · The paper itself

Abstract

rationaleSynthetic cathinones are used as stimulants of abuse. Different stimulants may induce distinct rates of disease progression, yielding neurochemical changes that may vary across brain regions or neurotransmitter systems.

objectivesThis research sought to behaviorally and chemically differentiate stages of synthetic cathinone abuse through rodent self-administration and measurement of the neurotransmitter profile in multiple brain regions.

methodsMale rats were trained to self-administer α-PVP, mephedrone (4MMC), or saline. Half of each drug group stopped self-administering after autoshaping; the other half self-administered for another 21 days. Brain tissue from amygdala, hippocampus, hypothalamus, PFC, striatum, and thalamus was profiled with electrochemical detection to assess neurotransmitter levels.

resultsDuring autoshaping, the majority of infusions were delivered noncontingently. In the self-administration phase, rats responded more for α-PVP and 4MMC than for saline, demonstrating that both synthetic cathinones were reinforcing. Longer durations of exposure elevated 5-HIAA in hypothalamus, PFC, and hippocampus, indicating that learning may produce changes in addiction-related brain regions. Both synthetic cathinones decreased norepinephrine in hippocampus, while α-PVP decreased glutamate in hippocampus and PFC, and 4MMC decreased glutamate in thalamus. Furthermore, α-PVP increased dopaminergic metabolites in striatum, whereas 4MMC decreased serotonin in the amygdala, hippocampus, and PFC. Interestingly, neither synthetic cathinone affected dopamine levels despite their functional effects on the dopaminergic system.

conclusionsIn summary, the neurotransmitter changes observed here suggest that synthetic cathinone use likely produces sequential neurochemical changes during the transition from use to abuse. Consequently, treatment need may differ depending on the progression of synthetic cathinone abuse.

Indexed as

AlkaloidsAnimalsBehavior, AddictiveBrainCentral Nervous System StimulantsMaleNeurotransmitter AgentsRatsRats, Sprague-DawleyReaction TimeReinforcement, PsychologySelf AdministrationSynthetic DrugsAlkaloidscathinoneCentral Nervous System StimulantsNeurotransmitter AgentsSynthetic DrugsMephedroneNeurotransmitterSelf-administrationα-PVP

Identifiers

PMID30191259
PMCPMC6401347
OpenAlexW2891590572

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.