Ketamine metabolite could inspire fast-acting antidepressants | May 5, 2016 Issue - Vol. 94 Issue 19 | Chemical & Engineering News
Volume 94 Issue 19 | p. 5 | News of The Week
Issue Date: May 9, 2016 | Web Date: May 5, 2016

Ketamine metabolite could inspire fast-acting antidepressants

New findings indicate that hydroxynorketamine is essential for the drug’s activity in mice
Department: Science & Technology
News Channels: Biological SCENE, Organic SCENE
Keywords: neuroscience, antidepressants, ketamine, hydroxynorketamine, GLYX-13, rapastinel
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Researchers deuterated the C6 carbon of ketamine (red star) to determine whether formation of the metabolite at right was necessary for the drug’s antidepressant activity.
Structures of ketamine and (2R,6R)-hydroxynorketamine.
 
Researchers deuterated the C6 carbon of ketamine (red star) to determine whether formation of the metabolite at right was necessary for the drug’s antidepressant activity.

Ketamine offers psychiatrists something that conventional antidepressants lack: speed. Most patients take selective serotonin reuptake inhibitors such as Prozac or Zoloft for weeks to months before they feel any improvement. But a single dose of ketamine can act within hours.

Unfortunately, the compound, used for decades as an anesthetic, comes with some downsides, including the potential for abuse as a psychedelic drug. So neuroscientists have tried to piece together ketamine’s antidepressant mechanism to help design new drugs.

A research team is now reporting that ketamine itself may not be involved in this mechanism. Studies in mice suggest instead that a hydroxylated metabolite is responsible for the antidepressant activity. This compound doesn’t block ketamine’s main target in the brain and doesn’t cause some of the drug’s known side effects (Nature 2016, DOI: 10.1038/nature17998).

“These exciting results, if confirmed by clinical studies, illuminate a clear pathway toward developing the next generation of rapid-acting antidepressants,” comments pharmacologist Irwin Lucki of the Uniformed Services University of the Health Sciences, who was not involved in the work.

In the study, scientists led by Todd D. Gould of the University of Maryland School of Medicine found that (2R,6R)-hydroxynorketamine (HNK) produced similar antidepressant effects as ketamine in mice in experiments that modeled different aspects of depression, including the loss of motivation to seek out pleasurable foods and scents after stress. Meanwhile, mice showed no signs of changes in sensory perception when given HNK, and the animals didn’t self-administer the compound, which would have been an indication of abuse potential.

To determine if the metabolite was necessary for ketamine’s antidepressant activity, the research team synthesized 6,6-dideuteroketamine, an analog that replaces two C–H bonds broken during ketamine metabolism with slightly stronger C–D bonds. “That difference is enough to make it a little harder to metabolize,” says team member Patrick J. Morris of the National Institutes of Health.

As a result, HNK levels in the brain of mice receiving the deuterated compound were lower compared with those getting ketamine. The analog produced little to no antidepressant effect in mice, demonstrating that forming HNK is necessary for ketamine’s activity.

In further studies, the team determined that HNK doesn’t inhibit the NMDA receptor—ketamine’s anesthetic target in the brain. Although the researchers haven’t found HNK’s specific target, they present evidence that suggests it could act through a pathway that activates signaling from a related receptor called AMPA.

“The target of ketamine’s antidepressant activity has often been assumed to be the NMDA receptor,” Gould says. “We show that’s not the case.” He also points out that attempts to develop novel fast-acting antidepressants by inhibiting the NMDA receptor have had limited success in clinical trials.

One molecule that has shown rapid antidepressant activity and is currently in clinical trials is rapastinel. Joseph R. Moskal of Northwestern University, who is chief scientific officer at biopharmaceutical company Aptinyx, discovered rapastinel, which activates AMPA receptor signaling via NMDA receptors. He thinks the ketamine metabolite findings reinforce a shift in thinking about ketamine’s antidepressant activity from NMDA-receptor inhibition toward other, possibly AMPA-related, pathways in the brain.

 
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