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Mephedrone (4-Methylmethcathinone)

Acute Behavioral Effects, Hyperthermic, and Pharmacokinetic Profile in Rats

Bibliographic Data

ID15518956
AuthorsKlára Šíchová (0000-0003-1653-822X, National Institute of Mental Health), Nikola Pinterová (0000-0001-6242-4413, National Institute of Mental Health), Monika Žídková (0000-0001-7891-277X, Charles University), Rachel R Horsley (0000-0003-2536-2465, National Institute of Mental Health), Eva Lhotková (National Institute of Mental Health), Kristýna Štefková (National Institute of Mental Health), Čestmír Vejmola (0000-0002-6434-5978, National Institute of Mental Health), Libor Uttl (0000-0003-0572-1213, Charles University), Marie Balı́ková (0000-0001-6334-1177, Charles University), Marie Balíková, Martin Kuchař (0000-0002-7616-6352, University of Chemistry and Technology, Prague), Tomáš Páleníček (0000-0002-3109-9539, Charles University, corresponding author)
Year2018
Volume8
Pages306-306
Publication date2018-01-10
Open AccessYes
TypeARTICLE
VenueFrontiers in Psychiatry (JOURNAL)
Journal identifiersISSN: 1664-0640 • E-ISSN: 1664-0640
PublisherFrontiers Media (PUBLISHER • CH)
DOI10.3389/fpsyt.2017.00306
PMID29375408
OpenAlexW2783399273
LanguageEN
Citations received1
References cited62

Mephedrone (MEPH) is a synthetic cathinone derivative with effects that mimic MDMA and/or cocaine. Our study in male Wistar rats provides detailed investigations of MEPH's and its primary metabolite nor-mephedrone's (nor-MEPH) pharmacokinetics and bio-distribution to four different substrates (serum, brain, lungs, and liver), as well as comparative analysis of their effects on locomotion [open field test (OFT)] and sensorimotor gating [prepulse inhibition of acoustic startle reaction (PPI ASR)]. Furthermore, in order to mimic the crowded condition where MEPH is typically taken (e.g., clubs), the acute effect of MEPH on thermoregulation in singly- and group-housed rats was evaluated. Pharmacokinetics of MEPH and nor-MEPH after MEPH (5 mg/kg, sc.) were analyzed over 8 h using liquid chromatography with mass spectrometry. MEPH (2.5, 5, or 20 mg/kg, sc.) and nor-MEPH (5 mg/kg, sc.) were administered 5 or 40 min before the behavioral testing in the OFT and PPI ASR; locomotion and its spatial distribution, ASR, habituation and PPI itself were quantified. The effect of MEPH on rectal temperature was measured after 5 and 20 mg/kg, sc. Both MEPH and nor-MEPH were detected in all substrates, with the highest levels detected in lungs. Mean brain: serum ratios were 1:1.19 (MEPH) and 1:1.91 (nor-MEPH), maximum concentrations were observed at 30 min; at 2 and 4 h after administration, nor-MEPH concentrations were higher compared to the parent drug. While neither of the drugs disrupted PPI, both increased locomotion and affected its spatial distribution. The effects of MEPH were dose dependent, rapid, and short-lasting, and the intensity of locomotor stimulant effects was comparable between MEPH and nor-MEPH. Despite the disappearance of behavioral effects within 40 min after administration, MEPH induced rectal temperature elevations that persisted for 3 h even in singly housed rats. To conclude, we observed a robust, short-lasting, and most likely synergistic stimulatory effect of both drugs which corresponded to brain pharmacokinetics. The dissociation between the duration of behavioral and hyperthermic effects is indicative of the possible contribution of nor-MEPH or other biologically active metabolites. This temporal dissociation may be related to the risk of prolonged somatic toxicity when stimulatory effects are no longer present

Biology · Drug · Mephedrone · Pharmacokinetics · Chemistry · Forensic Toxicology and Drug Analysis · Neurotransmitter Receptor Influence on Behavior · Psychedelics and Drug Studies · Pharmacology

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Citations per year0.17
Citation span2020 - 2020 (1)
Highly citedNo

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