NMDA Antagonists for Treatment-Resistant Depression.
Handbook of experimental pharmacology January 1, 2019 DOI: 10.1007/164_2018_165 via PubMed
Summary
AI-generated from the abstractNMDA antagonists, particularly ketamine, show promise for the 15-30% of patients with major depressive disorder who do not respond to monoaminergic antidepressants. A brief low-dose infusion of ketamine rapidly improves depressive symptoms for several days, though it produces psychotomimetic and cognitive side effects. Multiple infusions (e.g., 2-3 times per week for several weeks) provide relief, but symptoms return when treatment stops. A 96-hour higher-dose infusion with add-on clonidine mitigated side effects and resulted in about 40% of subjects still having a good response 8 weeks later, though this was a pilot study requiring confirmation. Nitrous oxide also showed positive results.
Study at a glance
| Characteristics | Review Pilot study Peer reviewed |
|---|---|
| Topics | Depression Ketamine |
| Keywords | Cerc-301 Memantine Nmda antagonists |
| Key finding | NMDA antagonists, especially ketamine, produce rapid but temporary antidepressant effects in treatment-resistant depression, with side effects that mirror therapeutic effects. |
Abstract
Fifteen to thirty percent of patients with major depressive disorder do not respond to antidepressants that target the monoaminergic systems. NMDA antagonists are currently being actively investigated as a treatment for these patients. Ketamine is the most widely studied of the compounds. A brief infusion of a low dose of this agent produces rapid improvement in depressive symptoms that lasts for several days. The improvement occurs after the agent has produced its well characterized psychotomimetic and cognitive side effects. Multiple infusions of the agent (e.g., 2-3× per week for several weeks) provide relief from depressive symptoms, but the symptoms reoccur once the treatment has been stopped. A 96-h infusion of a higher dose using add-on clonidine to mitigate the psychotomimetic effects appears to also provide relief and resulted in about 40% of the subjects still having a good response 8 weeks after the infusion. As this was a pilot study, additional work is needed to confirm and extend this finding. Nitrous oxide also has had positive results. Of the other investigational agents, CERC-301 and rapastinel remain in clinical development. When careful monitoring of neuropsychiatric symptoms has been conducted, these agents all produce similar side effects in the same dose range, indicating that NMDA receptor blockade produces both the wanted and unwanted effects. Research is still needed to determine the appropriate dose, schedule, and ways to mitigate against unwanted side effects of NMDA receptor blockade. These hurdles need to be overcome before ketamine and similar agents can be prescribed routinely to patients.