Evidence map›Paper›PMID 26769917›Full record

ArticleThe Journal of pharmacology and experimental therapeutics2016

Stereoselective Effects of Abused "Bath Salt" Constituent 3,4-Methylenedioxypyrovalerone in Mice: Drug Discrimination, Locomotor Activity, and Thermoregulation.

Brenda M Gannon, Adrian Williamson, Masaki Suzuki, Kenner C Rice, William E Fantegrossi

Abstract read
In one paragraph

Article in The Journal of pharmacology and experimental therapeutics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
–field-weighted citation impact
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

50 citing papers in PubMed.

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  11. Worsening of the Toxic Effects of (±)International journal of molecular sciences · 2021
    Article
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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

5 authors.

Brenda M GannonDepartment of Pharmacology and Toxicology (B.M.G., W.E.F.), College of Medicine (A.W.), University of Arkansas for Medical Sciences, Little Rock, Arkansas; and Drug Design and Synthesis Section, Chemical Biology Research Branch, National Institutes of Health National Institute on Drug Abuse and National Institute on Alcohol Abuse and Alcoholism, Bethesda, Maryland (M.S., K.C.R.).
Adrian WilliamsonDepartment of Pharmacology and Toxicology (B.M.G., W.E.F.), College of Medicine (A.W.), University of Arkansas for Medical Sciences, Little Rock, Arkansas; and Drug Design and Synthesis Section, Chemical Biology Research Branch, National Institutes of Health National Institute on Drug Abuse and National Institute on Alcohol Abuse and Alcoholism, Bethesda, Maryland (M.S., K.C.R.).
Masaki SuzukiDepartment of Pharmacology and Toxicology (B.M.G., W.E.F.), College of Medicine (A.W.), University of Arkansas for Medical Sciences, Little Rock, Arkansas; and Drug Design and Synthesis Section, Chemical Biology Research Branch, National Institutes of Health National Institute on Drug Abuse and National Institute on Alcohol Abuse and Alcoholism, Bethesda, Maryland (M.S., K.C.R.).
Kenner C RiceDepartment of Pharmacology and Toxicology (B.M.G., W.E.F.), College of Medicine (A.W.), University of Arkansas for Medical Sciences, Little Rock, Arkansas; and Drug Design and Synthesis Section, Chemical Biology Research Branch, National Institutes of Health National Institute on Drug Abuse and National Institute on Alcohol Abuse and Alcoholism, Bethesda, Maryland (M.S., K.C.R.).
William E FantegrossiDepartment of Pharmacology and Toxicology (B.M.G., W.E.F.), College of Medicine (A.W.), University of Arkansas for Medical Sciences, Little Rock, Arkansas; and Drug Design and Synthesis Section, Chemical Biology Research Branch, National Institutes of Health National Institute on Drug Abuse and National Institute on Alcohol Abuse and Alcoholism, Bethesda, Maryland (M.S., K.C.R.) WEFantegrossi@uams.edu.

Funding

PHYSIOLOGICAL DISTURBANCES ASSOCIATED WITH NEONATAL INTRAVENTRICULAR HEMORRHAGEP20RR020146 · NCRR · UNIV OF ARKANSAS FOR MED SCIS · PI GARCIA-RILL, EDGAR E. · 2004 to 2011
$17.2M
CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR029884 · NCRR · UNIV OF ARKANSAS FOR MED SCIS · PI LOWERY, CURTIS L · 2009 to 2011
$11.4M
Telemedicine CoreP30GM110702 · NIGMS · UNIV OF ARKANSAS FOR MED SCIS · PI GARCIA-RILL, EDGAR E. · 2014 to 2018
$6.1M
Translational Training in AddictionT32DA022981 · NIDA · UNIV OF ARKANSAS FOR MED SCIS · PI Melissa Jean Zielinski · 2009 to 2026
$6.1M
Medicinal Chemistry of Hallucinogenic DrugsZIADA000529 · NIDA · NATIONAL INSTITUTE ON DRUG ABUSE · PI RICE, KENNER · 2009 to 2016
$864k
Intramural NIH HHSNCRR NIH HHS P20 RR020146NCRR NIH HHS RR020146NCRR NIH HHS RR029884NCRR NIH HHS UL1 RR029884NIDA NIH HHS T32 DA022981NIDA NIH HHS T32DA022981NIGMS NIH HHS P30 GM110702
6 · The paper itself

Abstract

3,4-Methylenedioxypyrovalerone (MDPV) is a common constituent of illicit "bath salts" products. MDPV is a chiral molecule, but the contribution of each enantiomer to in vivo effects in mice has not been determined. To address this, mice were trained to discriminate 10 mg/kg cocaine from saline, and substitutions with racemic MDPV, S(+)-MDPV, and R(-)-MDPV were performed. Other mice were implanted with telemetry probes to monitor core temperature and locomotor responses elicited by racemic MDPV, S(+)-MDPV, and R(-)-MDPV under a warm (28°C) or cool (20°C) ambient temperature. Mice reliably discriminated the cocaine training dose from saline, and each form of MDPV fully substituted for cocaine, although marked potency differences were observed such that S(+)-MDPV was most potent, racemic MDPV was less potent than the S(+) enantiomer, and R(-)-MDPV was least potent. At both ambient temperatures, locomotor stimulant effects were observed after doses of S(+)-MDPV and racemic MDPV, but R(-)-MDPV did not elicit locomotor stimulant effects at any tested dose. Interestingly, significant increases in maximum core body temperature were only observed after administration of racemic MDPV in the warm ambient environment; neither MDPV enantiomer altered core temperature at any dose tested, at either ambient temperature. These studies suggest that all three forms of MDPV induce biologic effects, but R(-)-MDPV is less potent than S(+)-MDPV and racemic MDPV. Taken together, these data suggest that the S(+)-MDPV enantiomer is likely responsible for the majority of the biologic effects of the racemate and should be targeted in therapeutic efforts against MDPV overdose and abuse.

Indexed as

AnimalsBenzodioxolesBody Temperature RegulationDesigner DrugsDiscrimination LearningMaleMiceMotor ActivityPyrrolidinesStereoisomerismSynthetic CathinoneBenzodioxolesDesigner DrugsPyrrolidinesSynthetic Cathinone

Identifiers

PMID26769917
PMCPMC4767395

What OpenQuestion holds

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Registered trials

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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.