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NMDA Receptor Modulators in the Treatment of Drug Addiction
被引:45
|作者:
Tomek, Seven E.
[1
]
LaCrosse, Amber L.
[1
]
Nemirovsky, Natali E.
[1
]
Olive, M. Foster
[1
,2
]
机构:
[1] Arizona State Univ, Dept Psychol, Tempe, AZ 85287 USA
[2] Arizona State Univ, Interdisciplinary Grad Program Neurosci, Tempe, AZ 85287 USA
关键词:
glutamate;
N-methyl-D-aspartate receptor;
glycine binding site;
antagonist;
partial agonist;
D O I:
10.3390/ph6020251
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
Glutamate plays a pivotal role in drug addiction, and the N-methyl-D-aspartate (NMDA) glutamate receptor subtype serves as a molecular target for several drugs of abuse. In this review, we will provide an overview of NMDA receptor structure and function, followed by a review of the mechanism of action, clinical efficacy, and side effect profile of NMDA receptor ligands that are currently in use or being explored for the treatment of drug addiction. These ligands include the NMDA receptor modulators memantine and acamprosate, as well as the partial NMDA agonist D-cycloserine. Data collected to date suggest that direct NMDA receptor modulators have relatively limited efficacy in the treatment of drug addiction, and that partial agonism of NMDA receptors may have some efficacy with regards to extinction learning during cue exposure therapy. However, the lack of consistency in results to date clearly indicates that additional studies are needed, as are studies examining novel ligands with indirect mechanisms for altering NMDA receptor function.
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页码:251 / 268
页数:18
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