General Anesthesia Occludes Ketamine's Antidepressant Response in a Rodent Model of Chronic Stress.
Daniel Markman, Andrzej Z Wasilczuk, Joseph Michael Cichon
Psychedelic medicine (New Rochelle, N.Y.) December 1, 2024 DOI: 10.1089/psymed.2024.0007 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Animal experiment Peer reviewed |
|---|---|
| Population | Chronically stressed adult C57/BL6 male mice |
| Interventions | Ketamine isoflurane |
| Topics | Ketamine Esketamine |
| Keywords | Antidepressant response Chronic stress Dissociation General anesthesia Subjective effects Ketamine therapy Depression treatment Consciousness research Antidepressant mechanisms Psychedelic medicine |
| Citations | 2 |
| Key findings | Wakefulness is likely required for ketamine's rapid antidepressant responses, as coadministration of isoflurane eliminated ketamine's dissociative-like behavioral state, distinct neuronal activity patterns, and subsequent antidepressant-like effects. |
Abstract
Psychedelic-induced experiences are thought to play an important role in the therapeutic actions of rapid-acting antidepressants. General anesthesia is one scenario in which patients can be rendered unconscious and masked to the psychedelic treatment, providing a simple yet effective method to examine drug-induced changes in the brain devoid of experiences. Chronically stressed adult C57/BL6 male mice were given subhypnotic ketamine alone or ketamine and GABAergic anesthetic isoflurane at sedative (0.6%) and general anesthetic levels (1.2%). Behavioral testing and in vivo two-photon neuronal calcium responses were recorded at the time of drug administration. Antidepressant-like responses were recorded 24 h later. We find that both ketamine's dissociative-like behavioral state and distinct patterns of neuronal activity in pyramidal neurons of prefrontal cortex during administration are eliminated by the coadministration isoflurane at both doses. Following coexposure, both ketamine's antidepressant-like behavioral response and neuronal induction of activity-dependent molecular plasticity marker c-Fos fail to manifest. These findings provide behavioral and neurophysiological evidence that wakefulness is likely required for ketamine's rapid antidepressant responses. Thus, altering the level of consciousness to suppress psychedelic-induced experiences might impair activity-dependent plasticity mechanisms that confound the study of psychedelic-induced therapeutic effects.