TY  - JOUR
T1  - Comparative and interactive human psychopharmacologic effects of ketamine and amphetamine: Implications for glutamatergic and dopaminergic model psychoses and cognitive function
AU  - Krystal JH, Perry EB, Jr, Gueorguieva R, et al
Y1  - 2005/09/01
N1  - 10.1001/archpsyc.62.9.985
JO  - Archives of General Psychiatry
SP  - 985
EP  - 995
VL  - 62
IS  - 9
N2  - Background 
    In healthy individuals, ketamine hydrochloride and amphetamine sulfate produce cognitive, behavioral, and subjective effects resembling endogenous psychoses. Studying the comparative and interactive effects of these agents may provide insights into the roles of the glutamate and monoamine systems in psychosis and cognition.Objectives 
    To directly compare the effects of ketamine and amphetamine and to explore their interactive effects within individuals.Design 
    Placebo-controlled, randomized, double-blind psychopharmacologic trial.Setting and Participants 
    Forty-one healthy individuals recruited from the community who completed up to 4 test days.Main Outcome Measures 
    On each test day, participants received amphetamine (a 1-minute infusion of amphetamine sulfate, 0.25 mg/kg, or saline) and ketamine (a 1-minute intravenous infusion of ketamine, 0.23 mg/kg, followed by a 1-hour infusion of 0.5 mg/kg or an identical saline bolus and infusion). The order of amphetamine and ketamine infusions was randomized.Results 
    At the doses studied, ketamine and amphetamine produced positive symptoms and euphoria. However, perceptual changes were produced only by ketamine, and hostility, grandiosity, and somatic concern were stimulated only by amphetamine. Amphetamine and ketamine produced conceptual disorganization, but only ketamine produced concrete ideation and unusual mannerisms. Ketamine produced negative symptoms and disrupted delayed recall. Ketamine and amphetamine showed 3 types of interactive effects: (1) amphetamine attenuated the impairment of working memory produced by ketamine; (2) amphetamine and ketamine had additive effects on thought disorder, arousal, and euphoria; and (3) amphetamine and ketamine had less-than-additive effects on psychosis.Conclusions 
    These findings implicate N-methyl-D-aspartate glutamate receptors and dopamine systems in psychosis. However, glutamate and dopamine may differentially contribute to psychosis, thought disorder, and euphoria. Regarding medication development for cognitive dysfunction, the pattern of the interactive effects of ketamine and amphetamine is consistent with the hypothesis that facilitation of prefrontal cortical dopamine levels would attenuate some cognitive impairments associated with deficits in N-methyl-D-aspartate receptor function.
SN  - 0003-990X
M3  - doi: 10.1001/archpsyc.62.9.985
UR  - http://dx.doi.org/10.1001/archpsyc.62.9.985
ER  -