The purpose of this study is to determine whether the analgetic and other effects effect of ketamine are partly mediated through opioid receptors
Ketamine er et dissociative anaesthetic closely related with phencyclidine (PCP). Phencyclidine is a non-competitive NMDA-antagonist, and it is assumed that the pharmacodynamic mechanism of action for ketamine is the same. Receptor binding studies shows that ketamine has affinity to many receptor types, including opioid mu and kappa receptors. Ketamine has only about 25 times lower affinity for kappa receptors than for the NMDA-receptor complex. Naloxone is a specific antagonist for opioid receptors and block both mu og kappa receptors. A dose of naloxone 10 times larger than required to block mu receptors is required to block kappa receptors. Experiments with naloxone suggest that ketamine is not a mu agonist, but experiments with sufficient large naloxone doses to block kappa receptors have not been carried out in humans.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
QUADRUPLE
Enrollment
3
Saline single bolus dose followed by saline single bolus dose iv
Single bolus dose of saline followed by ketamine 0.2 mg/kg bw
Single bolus dose of naloxone 0.2 mg/kg bw followed by single bolus dose of saline
Ullevaal University Hospital
Oslo, Norway
Pain intensity (0-10 Numerical Rating Scale)
Time frame: 30 minutes
Subjective measurement of psychotomimetic effects
Time frame: 30 minutes
Adverse effects
Time frame: 30 minutes
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Single bolus dose of naloxone 0.2 mg/kg bw followed by single bolus dose of ketamine 0.2 mg/kg bw