Summary: Researchers report ketamine’s antidepressive effects require activation of opioid receptors in the brain. The study highlights the interaction between depression, pain and opioid addiction.
Scientists at the Stanford University School of Medicine have discovered that ketamine works as an antidepressant at least in part by activating the brain’s opioid system.
The finding overturns previously held beliefs that the drug’s antidepressant effects stemmed solely from its impact on the glutamate system. These beliefs led to the widespread use of ketamine to treat depression and spurred the development of glutamate-blocking drugs for use as antidepressants.
The new finding also highlights the interaction between depression, pain and opioid addiction and presents an opportunity for clinicians to reframe treatment approaches for three of the most important public health crises today.
The research is believed to be the first to address how ketamine works in the human brain to provide relief from depression. A paper describing the work was published Aug. 29 in The American Journal of Psychiatry.
“Before we did the study, I wasn’t sure that ketamine really worked to treat depression. Now I know the drug works, but it doesn’t work like everyone thought it was working,” said Alan Schatzberg, MD, the Kenneth T. Norris Jr. Professor of Psychiatry and Behavioral Sciences, who shares senior authorship of the paper with Carolyn Rodriguez, MD, PhD, assistant professor of psychiatry and behavioral sciences.
Ketamine was developed in the 1960s and has been used for decades as an anesthetic during surgery. It can cause dissociative side effects, including hallucinations, and has been used as a recreational drug. If used regularly, it can lead to dependence.
Although the Food and Drug Administration has not approved the drug’s use for depression, some doctors have prescribed it “off-label” in recent years as a rapid but short-acting antidepressant. Traditional antidepressants, such as selective serotonin reuptake inhibitors, take four to six weeks to have an effect but don’t work in two-thirds of patients who try them. Stand-alone ketamine clinics have popped up all over the country to administer expensive intravenous infusions of ketamine to patients, even though some scientists caution that not enough is known about the drug to warrant its widespread use for depression.
Ketamine infusions are also used to treat chronic pain, which is a common condition in depressed patients. Exactly how ketamine blunts pain is not fully understood, but it is known to work at least in part on the opioid system. The Stanford researchers wanted to see if the antidepressive effects of ketamine were also generated by ketamine’s activation of the opioid system. They sought to answer this question through a small clinical trial in which people with depression were given an opioid-receptor blocker prior to taking ketamine.
The study enrolled adults with treatment-resistant depression, meaning their condition had not improved after multiple treatment efforts. Twelve participants received infusions of ketamine twice — once preceded by naltrexone, an opioid-receptor blocker, and once with placebo. Neither the study participants nor the researchers were told whether active drug or placebo was administered during each test. The researchers found that ketamine reduced depressive symptoms by about 90 percent for three days in more than half of the participants when administered with a placebo, but had virtually no effect on depressive symptoms when it was preceded by naltrexone.
“This was purely a mechanistic study, not a treatment trial,” said Nolan Williams, MD, clinical assistant professor of psychiatry and behavioral science. “And the results were so clear that we ended the study early to avoid exposing additional patients to the ineffective combination treatment.” Williams shares lead authorship of the paper with Boris Heifets, MD, PhD, clinical assistant professor of anesthesiology, perioperative and pain medicine.
Because the field of anesthesia has long regarded ketamine specifically as a nonopioid drug, Heifets was skeptical when Williams approached him about joining the research effort. “Everything that I was taught, and everything that I’ve always taught my students — all of the evidence supports the fact that ketamine is not an opioid,” he said. “I was really surprised at the results.”
Understanding how it works
Although some small studies have shown that ketamine had rapid, although transient, antidepressant effects, Schatzberg said the researchers wanted to understand how ketamine works. He said he came to suspect that ketamine’s effects might be linked to the brain’s opioid system when Rodriguez published a report on ketamine’s ability to reduce symptoms of obsessive compulsive disorder, which was similar to previous Stanford research using the opioid morphine.
The prevailing hypothesis for ketamine’s antidepressant effect was that the drug blocked a receptor for glutamate, an excitatory neurotransmitter in the brain that is implicated in memory and learning. “But ketamine’s mechanism is complicated, as it acts on many different receptor types beyond glutamate receptors, and it acts in three distinct phases — rapid effects, sustained effects and return to baseline,” Rodriguez said.
Schatzberg noted that no other glutamate-receptor blocker has an antidepressant effect like ketamine and that attempts to develop similar drugs have largely failed.
The researchers said the findings from the new study may explain why ketamine works so quickly as an antidepressant: It activates the brain’s opioid receptors during its first phase of activity. The glutamate system may be responsible for the sustaining effects after ketamine is metabolized, they said.
The authors say that revealing the role of the opioid system in the antidepressant effects of ketamine is critical in the effort to develop new antidepressants. For instance, glutamate receptor blockers may not have rapid antidepressant effects unless they also involve the opioid system, Williams said.
“Psychiatry used opioids, barbiturates and high doses of stimulants to treat depression 50 or 60 years ago,” Schatzberg said. “We have to properly examine the risks associated with using drugs of abuse — even in low doses — to treat depression. It’s not limited to ketamine; other antidepressant drugs that target the opioid system are in development now, too.”
While a standard opioid like morphine initially has an antidepressant effect, it promotes depression after repeated use, Williams said. People who are depressed take as much as 2.4 times as many opioids immediately after painful surgeries than those who aren’t depressed, he said. “There is truly a link between depression, pain and opioid use,” Heifets said. “You can’t go after one without addressing the others.”
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Other Stanford co-authors of the study are research psychologist Christine Blasey, PhD; instructor Keith Sudheimer, PhD; medical student Jaspreet Pannu; life science researcher Heather Pankow; Jessica Hawkins, clinical research manager; Justin Birnbaum, MD, clinical professor of psychiatry; and David Lyons, PhD, professor of psychiatry. Lyons, Rodriguez and Schatzberg are members of the Stanford Neuroscience Institute. Schatzberg is also a member of Stanford Bio-X.
Rodriguez has consulted for Allergan, BlackThorn Therapeutics and Rugen Therapeutics. Schatzberg has consulted for Alkermes and Avanir, has equity in Corcept and Merck, and received a grant from Janssen Pharmaceuticals.
Funding: The study was funded by the National Institutes of Health (grant UL1TR001085 to Spectrum, the Stanford Center for Clinical and Translational Research and Education), the Brain and Behavior Research Foundation, the Avy L. and Roberta L. Miller Foundation and the Pritzker Family Fund.
Stanford’s Department of Psychiatry and Behavioral Sciences also supported the work.
Source: Kimber Price – Stanford Publisher: Organized by NeuroscienceNews.com. Image Source: NeuroscienceNews.com image is in the public domain. Original Research:Abstract for “Attenuation of Antidepressant Effects of Ketamine by Opioid Receptor Antagonism” by Nolan R. Williams, M.D., Boris D. Heifets, M.D., Ph.D., Christine Blasey, Ph.D., Keith Sudheimer, Ph.D., Jaspreet Pannu, B.S., Heather Pankow, B.S., Jessica Hawkins, B.S., Justin Birnbaum, M.D., David M. Lyons, Ph.D., Carolyn I. Rodriguez, M.D., Ph.D., and Alan F. Schatzberg, M.D. in The American Journal of Psychiatry. Published August 29 2018. doi:10.1176/appi.ajp.2018.18020138
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[cbtabs][cbtab title=”MLA”]Stanford”Ketamine’s Antidepressant Effects Tied to Opioid System in the Brain.” NeuroscienceNews. NeuroscienceNews, 29 August 2018. <http://neurosciencenews.com/opioid-system-ketamine-depression-9764/>.[/cbtab][cbtab title=”APA”]Stanford(2018, August 29). Ketamine’s Antidepressant Effects Tied to Opioid System in the Brain. NeuroscienceNews. Retrieved August 29, 2018 from http://neurosciencenews.com/opioid-system-ketamine-depression-9764/[/cbtab][cbtab title=”Chicago”]Stanford”Ketamine’s Antidepressant Effects Tied to Opioid System in the Brain.” http://neurosciencenews.com/opioid-system-ketamine-depression-9764/ (accessed August 29, 2018).[/cbtab][/cbtabs]
Attenuation of Antidepressant Effects of Ketamine by Opioid Receptor Antagonism
Objective: In addition to N-methyl-D-aspartate receptor antagonism, ketamine produces opioid system activation. The objective of this study was to determine whether opioid receptor antagonism prior to administration of intravenous ketamine attenuates its acute antidepressant or dissociative effects.
Method: In a proposed double-blind crossover study of 30 adults with treatment-resistant depression, the authors performed a planned interim analysis after studying 14 participants, 12 of whom completed both conditions in randomized order: placebo or 50 mg of naltrexone preceding intravenous infusion of 0.5 mg/kg of ketamine. Response was defined as a reduction ≥50% in score on the 17-item Hamilton Depression Rating Scale (HAM-D) score on postinfusion day 1.
Results: In the interim analysis, seven of 12 adults with treatment-resistant depression met the response criterion during the ketamine plus placebo condition. Reductions in 6-item and 17-item HAM-D scores among participants in the ketamine plus naltrexone condition were significantly lower than those of participants in the ketamine plus placebo condition on postinfusion days 1 and 3. Secondary analysis of all participants who completed the placebo and naltrexone conditions, regardless of the robustness of response to ketamine, showed similar results. There were no differences in ketamine-induced dissociation between conditions. Because naltrexone dramatically blocked the antidepressant but not the dissociative effects of ketamine, the trial was halted at the interim analysis.
Conclusions: The findings suggest that ketamine’s acute antidepressant effect requires opioid system activation. The dissociative effects of ketamine are not mediated by the opioid system, and they do not appear sufficient without the opioid effect to produce the acute antidepressant effects of ketamine in adults with treatment-resistant depression.
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