Evidence map›Paper›PMID 32500210›Full record

ArticlePsychopharmacology2020

Active vaccination reduces reinforcing effects of MDPV in male Sprague-Dawley rats trained to self-administer cocaine.

Samantha J McClenahan, Melinda G Gunnell, S Michael Owens, William E Fantegrossi

Open access · greenAbstract read
In one paragraph

Article in Psychopharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 45% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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.

Samantha J McClenahanDepartment of Pharmacology and Toxicology, College of Medicine, University of Arkansas for Medical Sciences, 4301 West Markham, Slot 638, Little Rock, AR, 72205, USA.
Melinda G GunnellDepartment of Pharmacology and Toxicology, College of Medicine, University of Arkansas for Medical Sciences, 4301 West Markham, Slot 638, Little Rock, AR, 72205, USA.
S Michael OwensDepartment of Pharmacology and Toxicology, College of Medicine, University of Arkansas for Medical Sciences, 4301 West Markham, Slot 638, Little Rock, AR, 72205, USA.
William E FantegrossiDepartment of Pharmacology and Toxicology, College of Medicine, University of Arkansas for Medical Sciences, 4301 West Markham, Slot 638, Little Rock, AR, 72205, USA. wefantegrossi@uams.edu.
University of Arkansas for Medical Sciences · US

Funding

Pharmacology and Therapy for MDPV and alpha-PVP Like Drugs of AbuseR01DA039195 · NIDA · UNIV OF ARKANSAS FOR MED SCIS · PI OWENS, SAMUEL MICHAEL · 2015 to 2018
$2.4M
Systems Pharmacology and Toxicology Training ProgramT32GM106999 · NIGMS · UNIV OF ARKANSAS FOR MED SCIS · PI PRATHER, PAUL L · 2013 to 2022
$1.4M
Development of Small-molecule Potentiators of Kir4.1/5.1 Potassium ChannelsF32DK127679 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MCCLENAHAN, SAMANTHA · 2021 to 2022
$86k
Development of an Enantiomeric Specific Vaccine for 3,4-Methylenedioxypyrovalerone (MDPV) AbuseF31DA046121 · NIDA · UNIV OF ARKANSAS FOR MED SCIS · PI MCCLENAHAN, SAMANTHA · 2018 to 2018
$35k
NIDA NIH HHS DA039195NIDA NIH HHS F31 DA046121NIDA NIH HHS F31DA046121NIDA NIH HHS R01 DA039195NIDDK NIH HHS F32 DK127679NIGMS NIH HHS GM106999NIGMS NIH HHS T32 GM106999
6 · The paper itself

Abstract

rationale3,4-Methylenedioxypyrovalerone (MDPV) is a synthetic cathinone abused for its cocaine-like psychostimulant effects in "bath salts" products. While there are currently no pharmacotherapies for MDPV abuse, rodent studies suggest immunotherapy may offer a feasible treatment option.

objectivesThese studies tested the capacity of active vaccination to reduce the reinforcing effects of MDPV in Sprague-Dawley rats.

methodsRats acquired cocaine self-administration (0.32 mg/kg/inf) on an FR1 schedule. Dose-effect functions for cocaine (0.032-1.0 mg/kg/inf) and MDPV (0.001-0.32 mg/kg/inf) were determined under an FR5 schedule. Rats in the vaccine group were immunized during cocaine self-administration. All rats transitioned to a progressive-ratio (PR) schedule to establish breakpoints for cocaine (0.1-1.0 mg/kg/inf) and MDPV (0.01-0.32 mg/kg/inf). Responding was extinguished, and cue-induced and MDPV-primed reinstatement (0.56 mg/kg, IP) were evaluated.

resultsNo endpoints of cocaine self-administration differed between groups, but the ED

conclusionsVaccination did not alter acquisition of cocaine self-administration, demonstrating pharmacological selectivity and suggesting that the vaccine did not affect learning or motivation, while effectively reducing the potency of MDPV as a reinforcer. The protective effects of the vaccine were surmounted by large unit doses of MDPV, suggesting maximal efficacy of drug-conjugate vaccines in substance abuse disorders will likely require concurrent behavior modification therapy.

Indexed as

Reinforcement, PsychologyAlkaloidsAnimalsBenzodioxolesCocaineDopamine Uptake InhibitorsDose-Response Relationship, DrugMalePyrrolidinesRatsRats, Sprague-DawleySelf AdministrationSubstance-Related DisordersSynthetic CathinoneVaccinationAlkaloidsBenzodioxolescathinoneCocaineDopamine Uptake InhibitorsPyrrolidinesSynthetic Cathinone3,4-MethylenedioxypyrovaleroneDrug-conjugate vaccineSelf-administration

Identifiers

PMID32500210
PMCPMC7502518
OpenAlexW3033306574

What Socratic 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 Socratic graph.