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Cocaine self-administration disrupted by the N-methyl-D-aspartate receptor antagonist ketamine: a randomized, crossover trial
by
Foltin, R W
, Dakwar, E
, Nunes, E V
, Hart, C L
, Levin, F R
in
692/699/476
/ 692/699/476/5
/ Adult
/ Behavioral Sciences
/ Biological Psychology
/ Brain-derived neurotrophic factor
/ Cell receptors
/ Central Nervous System Stimulants - pharmacology
/ Cocaine
/ Cocaine - pharmacology
/ Cocaine abuse
/ Cocaine-Related Disorders - drug therapy
/ Craving - drug effects
/ Cross-Over Studies
/ Cues
/ Dopamine
/ Drug therapy
/ Drug use
/ Female
/ Health aspects
/ Homeostasis
/ Hospitalization
/ Humans
/ Ketamine
/ Ketamine - metabolism
/ Ketamine - pharmacology
/ Ketamine - therapeutic use
/ Laboratory animals
/ Male
/ Medicine
/ Medicine & Public Health
/ Metabolites
/ Middle Aged
/ Motivation
/ Neurosciences
/ original-article
/ Pharmacotherapy
/ Psychiatry
/ Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors
/ Self Administration
/ Substance use disorder
/ Surgeons
/ Testing
2017
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Cocaine self-administration disrupted by the N-methyl-D-aspartate receptor antagonist ketamine: a randomized, crossover trial
by
Foltin, R W
, Dakwar, E
, Nunes, E V
, Hart, C L
, Levin, F R
in
692/699/476
/ 692/699/476/5
/ Adult
/ Behavioral Sciences
/ Biological Psychology
/ Brain-derived neurotrophic factor
/ Cell receptors
/ Central Nervous System Stimulants - pharmacology
/ Cocaine
/ Cocaine - pharmacology
/ Cocaine abuse
/ Cocaine-Related Disorders - drug therapy
/ Craving - drug effects
/ Cross-Over Studies
/ Cues
/ Dopamine
/ Drug therapy
/ Drug use
/ Female
/ Health aspects
/ Homeostasis
/ Hospitalization
/ Humans
/ Ketamine
/ Ketamine - metabolism
/ Ketamine - pharmacology
/ Ketamine - therapeutic use
/ Laboratory animals
/ Male
/ Medicine
/ Medicine & Public Health
/ Metabolites
/ Middle Aged
/ Motivation
/ Neurosciences
/ original-article
/ Pharmacotherapy
/ Psychiatry
/ Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors
/ Self Administration
/ Substance use disorder
/ Surgeons
/ Testing
2017
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Cocaine self-administration disrupted by the N-methyl-D-aspartate receptor antagonist ketamine: a randomized, crossover trial
by
Foltin, R W
, Dakwar, E
, Nunes, E V
, Hart, C L
, Levin, F R
in
692/699/476
/ 692/699/476/5
/ Adult
/ Behavioral Sciences
/ Biological Psychology
/ Brain-derived neurotrophic factor
/ Cell receptors
/ Central Nervous System Stimulants - pharmacology
/ Cocaine
/ Cocaine - pharmacology
/ Cocaine abuse
/ Cocaine-Related Disorders - drug therapy
/ Craving - drug effects
/ Cross-Over Studies
/ Cues
/ Dopamine
/ Drug therapy
/ Drug use
/ Female
/ Health aspects
/ Homeostasis
/ Hospitalization
/ Humans
/ Ketamine
/ Ketamine - metabolism
/ Ketamine - pharmacology
/ Ketamine - therapeutic use
/ Laboratory animals
/ Male
/ Medicine
/ Medicine & Public Health
/ Metabolites
/ Middle Aged
/ Motivation
/ Neurosciences
/ original-article
/ Pharmacotherapy
/ Psychiatry
/ Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors
/ Self Administration
/ Substance use disorder
/ Surgeons
/ Testing
2017
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Cocaine self-administration disrupted by the N-methyl-D-aspartate receptor antagonist ketamine: a randomized, crossover trial
Journal Article
Cocaine self-administration disrupted by the N-methyl-D-aspartate receptor antagonist ketamine: a randomized, crossover trial
2017
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Overview
Repeated drug consumption may progress to problematic use by triggering neuroplastic adaptations that attenuate sensitivity to natural rewards while increasing reactivity to craving and drug cues. Converging evidence suggests a single sub-anesthetic dose of the
N
-methyl-D-aspartate receptor antagonist ketamine may work to correct these neuroadaptations and restore motivation for non-drug rewards. Using an established laboratory model aimed at evaluating behavioral shifts in the salience of cocaine now vs money later, we found that ketamine, as compared to the control, significantly decreased cocaine self-administration by 67% relative to baseline at greater than 24 h post-infusion, the most robust reduction observed to date in human cocaine users and the first to involve mechanisms other than stimulant or dopamine agonist effects. These findings signal new directions in medication development for substance use disorders.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
/ Adult
/ Brain-derived neurotrophic factor
/ Central Nervous System Stimulants - pharmacology
/ Cocaine
/ Cocaine-Related Disorders - drug therapy
/ Cues
/ Dopamine
/ Drug use
/ Female
/ Humans
/ Ketamine
/ Male
/ Medicine
/ Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors
/ Surgeons
/ Testing
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