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Research article summary (published 12 Jul 2009):

Lack of cocaine self-administration in mice expressing a cocaine-insensitive dopamine transporter.

Full Abstract

Cocaine addiction is a worldwide public health problem for which there are no established treatments. The dopamine transporter (DAT) is suspected as the primary target mediating cocaine's abuse-related effects based on numerous pharmacological studies. However, in a previous study, DAT knockout mice were reported to self-administer cocaine, generating much debate regarding the importance of the DAT in cocaine's abuse-related effects. Here, we show that mice expressing a "knockin" of a cocaine-insensitive but functional DAT did not self-administer cocaine intravenously despite normal food-maintained responding and normal intravenous self-administration of amphetamine and a direct dopamine agonist. Our results have three implications. First, they imply a crucial role for high-affinity DAT binding of cocaine in mediating its reinforcing effects, reconciling mouse genetic engineering approaches with data from classic pharmacological studies. Second, they demonstrate the usefulness of knockin strategies that modify specific amino acid sequences within a protein. Third, they show that it is possible to alter the DAT protein sequence in such a way as to selectively target its interaction with cocaine, while sparing other behaviors dependent on DAT function. Thus, molecular engineering technology could advance the development of highly specialized compounds such as a dopamine-sparing "cocaine antagonist."

 

Author information

Author/s: Thomsen, Morgane (M); Han, Dawn D (DD); Gu, Howard H (HH); Caine, S Barak (SB);

Affiliation: Alcohol and Drug Abuse Research Center, McLean Hospital/Harvard Medical School, Belmont, MA 02478, USA. mthomsen(-atsign-)mclean.harvard.edu

Grants: R01-DA014610 (Agency:NIDA NIH HHS) ; R01-DA14644 (Agency:NIDA NIH HHS) ; R01-DA17323 (Agency:NIDA NIH HHS) ; R01-DA20124 (Agency:NIDA NIH HHS) ; R29-DA12142 (Agency:NIDA NIH HHS) ; T32-DA07232 (Agency:NIDA NIH HHS)

Journal and publication information

Publication Type: Comparative Study; Journal Article; Research Support, N.I.H., Extramural

Journal: The Journal of pharmacology and experimental therapeutics (J Pharmacol Exp Ther), published in United States. (Language: eng)

Reference: 2009-Oct; vol 331 (issue 1) : pp 204-11

Dates: Created 2009/09/23; Completed 2009/10/13; Revised 2009/11/03;

PMID: 19602552, status: MEDLINE (last retrieval date: 11/4/2009, IMS Date: )

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

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MeSH headings (categories)

This article was linked to the MESH Headings shown below.

Associated Chemicals: Dopamine Plasma Membrane Transport Proteins (0) ; Cocaine (50-36-2)

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