Evidence map›Paper›PMID 29971461›Full record

ArticlePsychopharmacology2019

Is the 3,4-methylendioxypyrovalerone/mephedrone combination responsible for enhanced stimulant effects? A rat study with investigation of the effect/concentration relationships.

Nadia Benturquia, Lucie Chevillard, Christophe Poiré, Olivier Roussel, Camille Cohier, Xavier Declèves, Jean-Louis Laplanche, Mélanie Etheve-Quelquejeu, Huixiong Chen, Bruno Mégarbane

Abstract read
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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. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
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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

10 authors at 2 institutions in 1 country.

Nadia BenturquiaInserm, UMR-S 1144, Paris-Descartes and Paris-Diderot Universities, Paris, France.
Lucie ChevillardInserm, UMR-S 1144, Paris-Descartes and Paris-Diderot Universities, Paris, France.
Christophe PoiréInserm, UMR-S 1144, Paris-Descartes and Paris-Diderot Universities, Paris, France.
Olivier RousselInserm, UMR-S 1144, Paris-Descartes and Paris-Diderot Universities, Paris, France.
Camille CohierInserm, UMR-S 1144, Paris-Descartes and Paris-Diderot Universities, Paris, France.
Xavier DeclèvesInserm, UMR-S 1144, Paris-Descartes and Paris-Diderot Universities, Paris, France.
Jean-Louis LaplancheInserm, UMR-S 1144, Paris-Descartes and Paris-Diderot Universities, Paris, France.
Mélanie Etheve-QuelquejeuCNRS, UMR8601, Laboratory of Chemistry and Pharmacological and Toxicological Biochemistry, CBNIT, Paris-Descartes University, Paris, France.
Huixiong ChenCNRS, UMR8601, Laboratory of Chemistry and Pharmacological and Toxicological Biochemistry, CBNIT, Paris-Descartes University, Paris, France.
Bruno MégarbaneInserm, UMR-S 1144, Paris-Descartes and Paris-Diderot Universities, Paris, France. bruno-megarbane@wanadoo.fr.ORCID http://orcid.org/0000-0002-2522-2764
Inserm · FRDélégation Paris 5 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleThe use of synthetic cathinones as recreational drugs frequently sold in combination has been increasing exponentially. However, the consequences of combining cathinones on the resulting stimulant effects and the pharmacokinetics have been poorly investigated. OBJECTIVE AND

methodsTo study 3,4-methylenedioxypyrovalerone (MDPV; 3 mg/kg) and mephedrone (4-MMC; 30 mg/kg)-induced effects on rat locomotor activity and pharmacokinetics, administered alone or in combination by the intragastric route. The pharmacokinetic parameters were determined using non-compartmental analysis and the relationships between the locomotor activity and drug concentrations using sigmoidal E

resultsLocomotor activity significantly increased during the first hour post-administration with the MDPV/4-MMC combination in comparison to MDPV (p < 0.001) and 4-MMC (p < 0.01) alone. The pharmacokinetic profile of MDPV, but not 4-MMC, was significantly modified with the combination resulting in decreases in C

conclusionAn MDPV/4-MMC combination results in enhanced stimulant effects in the rat, despite significant reduction in MDPV bioavailability. Enhanced effects could be explained by increased MDPV distribution and/or possible complementation at the brain dopaminergic targets. However, the exact consequences of the MDPV/4-MMC combination in humans remain to be clarified.

Indexed as

AnimalsBenzodioxolesCentral Nervous System StimulantsDopamine Uptake InhibitorsDose-Response Relationship, DrugIllicit DrugsLocomotionMaleMethamphetaminePsychotropic DrugsPyrrolidinesRandom AllocationRatsRats, Sprague-DawleySynthetic CathinoneBenzodioxolesCentral Nervous System StimulantsDopamine Uptake InhibitorsIllicit DrugsmephedroneMethamphetaminePsychotropic DrugsPyrrolidinesSynthetic Cathinone4-MMCEffect/concentration relationshipsLocomotor activityMDPVPharmacokinetics

Identifiers

PMID29971461
OpenAlexW2810747638

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.