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Neurobiology of 3,4-methylenedioxypyrovalerone (MDPV) and α-pyrrolidinovalerophenone (α-PVP)

Journal

BRAIN RESEARCH BULLETIN
Volume 126, Issue -, Pages 111-126

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.brainresbull.2016.04.011

Keywords

Synthetic cathinones; Mechanism of action; Structure-activity relationships (SAR); Metabolism; Behavioral studies

Categories

Funding

  1. U.S. Public Health Services [DA-033930]

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Synthetic cathinones are analogs of cathinone or beta-ketoamphetamine - the major psychostimulant component of the shrub Catha edulis or khat. Cathinone analogs - though not termed as such - have been known for >100 years, but confusing chemical nomenclature often made the topic difficult to appreciate. In addition, many of the early analogs were prepared as synthetic precursors for the development of various other agents, and relatively few were pharmacologically evaluated. Cathinone is a close structural relative of amphetamine. Today, certain cathinone derivatives, synthetic cathinones, are known to produce central stimulant actions and represent a new class of drugs of abuse. Depending upon the nature of their terminal amine, a substituent, and aryl substituents, they seem to produce their effects via release or reuptake of various neurotansmitters including dopamine norepinephreine and/or serotonin. Two of the newest and most prominent members of the class are MDPV and its parent alpha-PVP (flakka). Both have been encountered on their own and in what might be constituents of what has been termed by a variety of names including psychoactive bath salts. Here, we describe the nomenclature of synthetic cathinones, the mechanism(s) of action of MDPV and alpha-PVP, and their structure-activity relationships. In order to assist in forensic studies, and to identify novel substances requiring future pharmacological evaluation, the metabolism of these agents is also described. Finally, the preclinical behavioral actions of these two agents in a variety of behavioral assays, including rodent locomotor assays, self-administration studies, intracranial self-stimulation, conditioned place preference, and drug discrimination, is summarized. The results of these studies with MDPV and a-PVP are consistent with their acting as potent cocaine-like central stimulants with abuse liability. (C) 2016 Elsevier Inc. All rights reserved.

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