New study shows how ketamine combats depression
Karolinska Institutet Jun 03, 2020
In the first phase of the study, 30 people with difficult-to-treat depression were randomly assigned to either a ketamine-infusion group (20 individuals) or a placebo (saline) group. It was a randomised double-blind study, so neither patient nor doctor initially knew who received the active substance. The participants’ brains were imaged with a PET camera before the infusion and 24-72 hours afterwards.
In the next phase, those who so wished (29 individuals) received ketamine twice a week for 2 weeks. The result was that over 70% of those treated with ketamine responded to the drug according to a rating scale for depression.
Increases the number of receptors
Serotonin plays a key role in depression and low levels are thought to be linked to more serious disease. There are 14 different kinds of receptor for this neurotransmitter on the surface of neurons. For their PET imaging, the researchers used a radioactive marker that binds specifically to serotonin 1B receptors. They found that the ketamine operated via these receptors in a formerly unknown mechanism of action. Binding to this receptor reduces the release of serotonin but increases that of another neurotransmitter called dopamine. Dopamine is part of the brain’s reward system and helps people to experience positive feelings about life, something that is often lacking in depression.
“We show for the first time that ketamine treatment increases the number of serotonin 1B receptors,” says the study’s last author Johan Lundberg, research group leader at the Department of Clinical Neuroscience, Karolinska Institutet. “Ketamine has the advantage of being very rapid-acting, but at the same time it is a narcotic-classed drug that can lead to addiction. So it’ll be interesting to examine in future studies if this receptor can be a target for new, effective drugs that don’t have the adverse effects of ketamine.”
The study was conducted in association with North Stockholm Psychiatry and was financed by the Swedish Research Council, the Söderström König Foundation, the Centre for Psychiatry Research, Region Stockholm, the Swedish Psychiatric Foundation and Karolinska Institutet.
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