DARK Classics in Chemical Neuroscience: Cathinone-Derived Psychostimulants.
ACS Chem Neurosci. 2018 10 17; 9(10):2379-2394.AC

Abstract

Cathinone is a plant alkaloid found in khat leaves of perennial shrubs grown in East Africa. Similar to cocaine, cathinone elicits psychostimulant effects which are in part attributed to its amphetamine-like structure. Around 2010, home laboratories began altering the parent structure of cathinone to synthesize derivatives with mechanisms of action, potencies, and pharmacokinetics permitting high abuse potential and toxicity. These "synthetic cathinones" include 4-methylmethcathinone (mephedrone), 3,4-methylenedioxypyrovalerone (MDPV), and the empathogenic agent 3,4-methylenedioxymethcathinone (methylone) which collectively gained international popularity following aggressive online marketing as well as availability in various retail outlets. Case reports made clear the health risks associated with these agents and, in 2012, the Drug Enforcement Agency of the United States placed a series of synthetic cathinones on Schedule I under emergency order. Mechanistically, cathinone and synthetic derivatives work by augmenting monoamine transmission through release facilitation and/or presynaptic transport inhibition. Animal studies confirm the rewarding and reinforcing properties of synthetic cathinones by utilizing self-administration, place conditioning, and intracranial self-stimulation assays and additionally show persistent neuropathological features which demonstrate a clear need to better understand this class of drugs. This Review will thus detail (i) historical context of cathinone use and the rise of "dark" synthetic derivatives, (ii) structural features and mechanisms of synthetic cathinones, (iii) behavioral effects observed clinically and in animals under controlled laboratory conditions, and (iv) neurotransmitters and circuits that may be targeted to manage synthetic cathinone abuse in humans.

Links

Publisher Full Text
ncbi.nlm.nih.gov
dx.doi.org
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Authors+Show Affiliations

Simmons SJ
Center for Substance Abuse Research (CSAR) , Lewis Katz School of Medicine at Temple University , Philadelphia , Pennsylvania 19140 , United States.
Leyrer-Jackson JM
Department of Psychology , Arizona State University , Tempe , Arizona 85281 , United States.
Oliver CF
Center for Substance Abuse Research (CSAR) , Lewis Katz School of Medicine at Temple University , Philadelphia , Pennsylvania 19140 , United States.
Hicks C
Center for Substance Abuse Research (CSAR) , Lewis Katz School of Medicine at Temple University , Philadelphia , Pennsylvania 19140 , United States.
Muschamp JW
Center for Substance Abuse Research (CSAR) , Lewis Katz School of Medicine at Temple University , Philadelphia , Pennsylvania 19140 , United States.
Rawls SM
Center for Substance Abuse Research (CSAR) , Lewis Katz School of Medicine at Temple University , Philadelphia , Pennsylvania 19140 , United States.
Olive MF
Department of Psychology , Arizona State University , Tempe , Arizona 85281 , United States.

MeSH

AlkaloidsAnimalsBehavior, AnimalBenzodioxolesBody TemperatureCathaCentral Nervous System StimulantsDopamineHistory, 21st CenturyHistory, MedievalHumansLocomotionMethamphetaminePyrrolidinesSerotoninSubstance-Related DisordersSynaptic Transmission

Pub Type(s)

Historical Article
Journal Article
Research Support, N.I.H., Extramural
Review

Language

eng

PubMed ID

29714473