In this study, the investigators examine the effects of low-dose ketamine on different oculomotor, perceptual and cognitive functions. They also examine effects on concurrent brain activity using blood oxygen level dependent (BOLD) functional magnetic resonance imaging (fMRI). A sample of N=25 healthy, male participants is required to complete the study. The design is within-subjects, placebo-controlled, double-blind and cross-over. A targeted ketamine level in plasma of 100ng/ml is applied. It is hypothesised that ketamine, compared to placebo, will lead to changes in task performance and brain activity similar to those observed in patients with schizophrenia.
The uncompetitive N-methyl-D-aspartate (NMDA) receptor antagonist ketamine has been proposed as a model system of the symptoms of schizophrenia. To complement this model system and to allow neurobiological as well as translational studies, biomarkers are often applied to people under the influence of ketamine. Here, we apply oculomotor, perceptual and cognitive biomarkers to healthy human volunteers whilst they undergo BOLD fMRI at 3 Tesla field strength. We use a counter-balanced, placebo-controlled, double-blind, within-subjects design. A sample of 25 healthy participants is required. Participants will receive intravenous (IV) racemic ketamine (with a 100ng/ml target plasma concentration) on one of two assessment days and they will receive placebo (intravenous saline) on the other assessment day. BOLD fMRI will be carried out on a Siemens Trio scanner at the Life\&Brain Centre, Bonn. In addition to brain functional and cognitive, perceptual and oculomotor responses, we will also measure self-ratings of psychosis-like experiences. These will be obtained using the Psychotomimetic States Inventory (PSI; Mason et al 2008).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
TRIPLE
Enrollment
24
University of Bonn
Bonn, North Rhine-Westphalia, Germany
Brain activity in cortical and subcortical areas as assessed using BOLD (blood oxygen level dependent) functional magnetic resonance imaging (fMRI) at 3 Tesla field strength
Time frame: within 1 hour of start of IV infusion
Psychotomimetic State Inventory (PSI)
Time frame: within 1 hour of start of IV infusion
Visual Analogue Rating Scales (VARS) from Norris 1971; self-rating scores of the subscales "mental sedation", "physical sedation", "tranquillisation" and "other feelings and attitudes"
Time frame: within 1 hour of start of IV infusion
d2 Attention Test, a measure of sustained attention
The test requires the crossing out of the letter d combined with two dashes amidst letters d and p combined with one, two, three or four dashes and is a well-established measure of sustained attention
Time frame: within 1 hour of start of IV infusion
Recognition memory performance (latencies in ms)
Time frame: after 5 days of washout period
Recognition memory performance (percent correct responses)
Time frame: after 5 days of washout period
Smooth pursuit gain (%)
Time frame: within 1 hour of start of IV infusion
Smooth pursuit root mean square error (RMSE)
Time frame: within 1 hour of start of IV infusion
Smooth pursuit saccadic frequency (number per second)
Time frame: within 1 hour of start of IV infusion
Prosaccade latency (ms)
Time frame: within 1 hour of start of IV infusion
Prosaccade gain (%)
Time frame: within 1 hour of start of IV infusion
Prosaccade spatial error (%)
Time frame: within 1 hour of start of IV infusion
Prosaccade velocity (degrees per second)
Time frame: within 1 hour of start of IV infusion
Prosaccade error rate (%)
Time frame: within 1 hour of start of IV infusion
Antisaccade latency (ms)
Time frame: within 1 hour of start of IV infusion
Antisaccade gain (%)
Time frame: within 1 hour of start of IV infusion
Antisaccade spatial error (%)
Time frame: within 1 hour of start of IV infusion
Antisaccade velocity (degrees per second)
Time frame: within 1 hour of start of IV infusion
Antisaccade error rate (%)
Time frame: within 1 hour of start of IV infusion
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