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Molecular Pharmacology Fast Forward
First published on December 21, 2007; DOI: 10.1124/mol.107.044586


0026-895X/08/7303-616-618$20.00
Mol Pharmacol 73:616-618, 2008

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Perspective

Distinctions between Dopamine Transporter Antagonists Could be Just around the Bend

L. Keith Henry, and Randy D. Blakely

Departments of Pharmacology (L.K.H., R.D.B.) and Psychiatry (R.D.B.), Centers for Structural Biology (L.K.H.) and Molecular Neuroscience (R.D.B.), Vanderbilt University, Nashville, Tennessee

Abuse of psychostimulants such as cocaine and amphetamines has a tremendous social and economic impact. Although replacement therapies are offered for addiction to opioids, nicotine, and alcohol, there is no approved replacement treatment for psychostimulant addiction. Recent studies on an emerging group of benztropine- and rimcazole-based compounds provide hope that replacement therapies for cocaine and amphetamine addiction may come in the near future. A new study (p. 813) now investigates the molecular interaction of the benztropine and rimcazole compounds with their target, the dopamine transporter, and provides an intriguing explanation as to why use of these compounds, unlike cocaine, do not lead to locomotor stimulation and drug discrimination behaviors in animal models.


Received December 21, 2007; accepted December 21, 2007

Address correspondence to: Dr. L. Keith Henry, Department of Pharmacology, Physiology, and Therapeutics, University of North Dakota School of Medicine and Health Sciences, Grand Forks, ND 58203. E-mail: khenry{at}medicine.nodak.edu


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MolPharm 2008 73: 813-823. [Abstract] [Full Text]  






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