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The Ketamine Antidepressant Story: New Insights

Tahani K. Alshammari

Molecules December 7, 2020 DOI: 10.3390/molecules25235777 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Review Peer reviewed
Intervention Ketamine
Dose single subanesthetic dose
Topics Esketamine Ketamine
Key findings Argues that ketamine's rapid and sustained antidepressant effects, achieved with a single subanesthetic dose, challenge the monoamine theory of depression and point to new molecular pathways. The authors propose that hydroxynorketamine metabolites and other dose-dependent mechanisms warrant further study to inform development of novel antidepressants for treatment-resistant depression.

Abstract

Ketamine is a versatile agent primarily utilized as a dissociative anesthetic, which acts by blocking the excitatory receptor N-methyl-d-aspartate receptor (NMDA). It functions to inhibit the current of both Na+ and K+ voltage-gated channels, thus preventing serotonin and dopamine reuptake. Studies have indicated that administering a single subanesthetic dose of ketamine relieves depression rapidly and that the effect is sustained. For decades antidepressant agents were based on the monoamine theory. Although ketamine may not be the golden antidepressant, it has opened new avenues toward mechanisms involved in the pathology of treatment-resistant depression and achieving rapid antidepressant effects. Thus, preclinical studies focusing on deciphering the molecular mechanisms involved in the antidepressant action of ketamine will assist in the development of a new antidepressant. This review was conducted to elucidate the emerging pathways that can explain the complex dose-dependent mechanisms achieved by administering ketamine to treat major depressive disorders. Special attention was paid to reviewing the literature on hydroxynorketamines, which are ketamine metabolites that have recently attracted attention in the context of depression.

Comparable studies

Other narrative reviews on ketamine, most cited first.

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