TY - JOUR
T1 - DARK Classics in Chemical Neuroscience
T2 - Cathinone-Derived Psychostimulants
AU - Simmons, Steven J.
AU - Leyrer-Jackson, Jonna M.
AU - Oliver, Chicora F.
AU - Hicks, Callum
AU - Muschamp, John
AU - Rawls, Scott M.
AU - Olive, Michael
N1 - Funding Information:
*Mailing address: Center for Substance Abuse Research, Lewis Katz School of Medicine, Temple University, 3500 North Broad Street, MERB 881A, Philadelphia, PA, 19140. Tel: 856-571-3894. E-mail: steven.james.simmons@gmail.com. ORCID Steven J. Simmons: 0000-0002-6982-4740 Callum Hicks: 0000-0002-6144-8883 Author Contributions S.J.S. outlined, contributed to, corroborated, and edited the manuscript under direction of S.M.R. and M.F.O. J.M.L.-J., C.F.O., C.H., S.M.R., and M.F.O. contributed written sections to the manuscript. J.W.M. composed graphics for the manuscript. Funding The authors acknowledge generous support from the National Institute on Drug Abuse (R01 DA039139 awarded to S.M.R. and R01 DA043172 awarded to M.F.O.). Notes The authors declare no competing financial interest.
Publisher Copyright:
© Copyright 2018 American Chemical Society.
PY - 2018/10/17
Y1 - 2018/10/17
N2 - 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.
AB - 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.
KW - Addiction
KW - cathinone
KW - designer drugs
KW - dopamine
KW - novel psychoactive substance(s)
KW - reward
KW - synthetic cathinone(s)
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U2 - 10.1021/acschemneuro.8b00147
DO - 10.1021/acschemneuro.8b00147
M3 - Review article
C2 - 29714473
AN - SCOPUS:85046532718
SN - 1948-7193
VL - 9
SP - 2379
EP - 2394
JO - ACS Chemical Neuroscience
JF - ACS Chemical Neuroscience
IS - 10
ER -