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4 ffects on hippocampal synaptic function at a subanesthetic, but therapeutically relevant concentratio
5 3 cells stably transfected with hL1, whereas subanesthetic concentrations of 3-azioctanol (14 microM)
8 hat 1-octanol inhibited native T-currents at subanesthetic concentrations with an IC(50) of approxima
11 in regional brain metabolism induced by the subanesthetic dose may be relevant to effects of ketamin
16 pressant and antisuicidal effect of a single subanesthetic dose of ketamine infusion for treatment-re
18 ance imaging to investigate the effects of a subanesthetic dose of ketamine on measures of functional
19 transmission that is reversible by an acute, subanesthetic dose of ketamine, along with regionally se
21 A, n = 25) during intravenous infusion of a subanesthetic dose of ketamine, compared to normal salin
22 e been observed in nonhuman primates after a subanesthetic dose of ketamine, including an impairment
23 se in glutamine/glutamate ratios to a single subanesthetic dose of ketamine, which mirrors the time c
27 widely replicated observation that a single subanesthetic dose of the N-methyl-D-aspartate glutamate
28 e observed in select brain regions after the subanesthetic dose, an anesthetic dose of ketamine (100
29 ast, ketamine, when administered as a single subanesthetic dose, exerts rapid and sustained antidepre
30 NMDA antagonist ketamine, when injected at a subanesthetic dose, produces working memory deficit and
32 supports the use of-or further research with-subanesthetic-dose ketamine and its (S)-enantiomer esket
33 n, evidence of an antidepressant response to subanesthetic-dose ketamine has led to a collection of s
34 pharmacology and hypothesized mechanisms of subanesthetic-dose ketamine in clinical research; 2) des
35 tly administered relatively low and moderate subanesthetic doses (<1 mg/kg approximate human intraven
38 ntidepressant properties of a broad range of subanesthetic doses of IV ketamine among outpatients wit
39 the efficacy of the 0.5 mg/kg and 1.0 mg/kg subanesthetic doses of IV ketamine and no clear or consi
40 in healthy volunteers (N = 10) who received subanesthetic doses of ketamine and in a group of clinic
42 nkeys before and after the administration of subanesthetic doses of ketamine during the performance o
44 esent investigation show that anesthetic and subanesthetic doses of ketamine have pronounced effects
45 nkeys before and after the administration of subanesthetic doses of ketamine in a rule-based working
46 s previously demonstrated, administration of subanesthetic doses of ketamine increased 2-DG uptake in
49 f dopamine D(1A) receptors in the effects of subanesthetic doses of ketamine on both behavioral respo
52 he antidepressant and anti-stress effects of subanesthetic doses of ketamine, an NMDA receptor antago
53 ate release, following the administration of subanesthetic doses of ketamine, are related to the drug
55 n sought to define brain regions affected by subanesthetic doses of ketamine, using high resolution a
63 ional and neutral slides while under various subanesthetic doses of sevoflurane or placebo (no anesth
71 t study, the authors tested whether a single subanesthetic infusion of ketamine administered to adult
73 uthors tested the acute effect of adjunctive subanesthetic intravenous ketamine on clinically signifi
74 lved an anaesthesiologist infusing a single, subanesthetic, intravenous dose, and required hospitaliz
75 for such disparate findings by administering subanesthetic ketamine (1-30 mg/kg, i.v.) or vehicle to
76 tudies have found that repeated or high-dose subanesthetic ketamine administration results in consist
82 egative beliefs maintain depression and that subanesthetic ketamine infusions induce rapid antidepres
83 This investigation examined the effects of subanesthetic ketamine infusions on motivation for quitt
88 cillatory activity are widely reported after subanesthetic ketamine, however their mechanisms of gene