Ketamine's acute effects on negative brain states are mediated through distinct altered states of consciousness in humans
This placebo-controlled study (n=13) investigated the effects of ketamine (3.5-35mg/70kg) on altered states of consciousness (ASCs) and their neural mechanisms. It examined the impact of different doses of ketamine on emotional task-evoked brain activity and various components of dissociation and ASCs. The study found that ketamine-induced ASCs had differential effects on brain activity, with higher depersonalization relieving negative brain states, while dissociative amnesia exacerbated insula activity. These results may provide insights into how specific dissociative states predict the response to ketamine in individuals with depression.
Authors
- Boris Heifets
- Trisha Suppes
- Xue Zhang
Published
Abstract
Ketamine commonly and rapidly induces dissociative and other altered states of consciousness (ASCs) in humans. However, the neural mechanisms that contribute to these experiences remain unknown. We used functional neuroimaging to engage key regions of the brain’s affective circuits during acute ketamine-induced ASCs within a randomized, multi-modal, placebo-controlled design examining placebo, 0.05 mg/kg ketamine, and 0.5 mg/kg ketamine in nonclinical adult participants (NCT03475277). Licensed clinicians monitored infusions for safety. Linear mixed effects models, analysis of variance, t-tests, and mediation models were used for statistical analyses. Our design enabled us to test our pre-specified primary and secondary endpoints, which were met: effects of ketamine across dose conditions on (1) emotional task-evoked brain activity, and (2) sub-components of dissociation and other ASCs. With this design, we also could disentangle which ketamine-induced affective brain states are dependent upon specific aspects of ASCs. Differently valenced ketamine-induced ASCs mediated opposing effects on right anterior insula activity. Participants experiencing relatively higher depersonalization induced by 0.5 mg/kg of ketamine showed relief from negative brain states (reduced task-evoked right anterior insula activity, 0.39 SD). In contrast, participants experiencing dissociative amnesia showed an exacerbation of insula activity (0.32 SD). These results in nonclinical participants may shed light on the mechanisms by which specific dissociative states predict response to ketamine in depressed individuals.
Research Summary of 'Ketamine's acute effects on negative brain states are mediated through distinct altered states of consciousness in humans'
Introduction
Hack and colleagues situate this study within a growing literature showing that subanesthetic ketamine commonly produces dissociative and other altered states of consciousness (ASCs) while also producing rapid changes in affective neural circuits and, in clinical samples, fast antidepressant effects. Prior work demonstrates that ketamine engages nodes of a negative affect circuit—particularly the anterior insula, amygdala, and anterior cingulate cortex (ACC)—but it remains unclear whether acute changes in neural activity in these regions depend on specific subjective ASCs. The authors note that dissociative experiences are heterogeneous, spanning states that may relieve negative affect (for example depersonalization or blissful states) and states that may be aversive (for example amnesia, anxiety, impaired control), and argue that separating these subcomponents is important for understanding ketamine's mechanisms and therapeutic effects.
Expert Research Summaries
Go Pro to access AI-powered section-by-section summaries, editorial takes, and the full research toolkit.
Full Text PDF
Full Paper PDF
Pro members can view the original manuscript directly in the browser.
Study Details
- Study Typeindividual
- Journal
- Compounds
- Topics
- Authors
- APA Citation
Hack, L. M., Zhang, X., Heifets, B. D., Suppes, T., van Roessel, P. J., Yesavage, J. A., Gray, N. J., Hilton, R., Bertrand, C., Rodriguez, C. I., Deisseroth, K., Knutson, B., & Williams, L. M. (2023). Ketamine's acute effects on negative brain states are mediated through distinct altered states of consciousness in humans. Nature Communications, 14(1). https://doi.org/10.1038/s41467-023-42141-5
References (20)
Papers cited by this study that are also in Blossom
Berman, R. M., Cappiello, A., Anand, A. et al. · Biological Psychiatry (2000)
Jones, J. L., Mateus, C. F., Malcolm, R. J. et al. · Frontiers in Psychiatry (2018)
Whittaker, E., Dadabayev, A. R., Joshi, S. A. et al. · Therapeutic Advances in Psychopharmacology (2021)
Cao, D., Yu, J., Wang, H. et al. · Science (2022)
Ionescu, D. F., Felicione, J. M., Gosai, A. et al. · Harvard Review of Psychiatry (2018)
Alexander, L., Jelen, L. A., Mehta, M. A. et al. · Neuroscience and Biobehavioral Reviews (2021)
Zarate, C. A., Brutsche, N. E., Ibrahim, L. et al. · Biological Psychiatry (2012)
Lally, N., Nugent, A. C., Luckenbaugh, D. A. et al. · Translational Psychiatry (2014)
Niciu, M. J., Shovestul, B. J., Jaso, B. A. et al. · Journal of Affective Disorders (2018)
Sumner, R. L., Chacko, E., Mcmillan, R. et al. · Journal of Psychopharmacology (2021)
Show all 20 referencesShow fewer
Reed, L. J., Nugent, A. C., Furey, M. et al. · NeuroImage (2018)
Reed, L. J., Nugent, A. C., Furey, M. et al. · Biological Psychiatry (2019)
Murrough, J. W., Perez, A. M., Pillemer, S. et al. · Biological Psychiatry (2012)
Luckenbaugh, D. A., Niciu, M. J., Ionescu, D. F. et al. · Journal of Affective Disorders (2014)
Mollaahmetoglu, O. M., Keeler, J., Ashbullby, K. J. et al. · Frontiers in Psychiatry (2021)
Mcinnes, L. A., Qian, J. J., Gargeya, R. S. et al. · Journal of Affective Disorders (2022)
Mcintyre, R. S., Rosenblat, J. D., Nemeroff, C. B. et al. · American Journal of Psychiatry (2021)
Nugent, A. C., Ballard, E. D., Gould, T. D. et al. · Molecular Psychiatry (2018)
Van Schalkwyk, G. I., Wilkinson, S. T., Davidson, L. et al. · Journal of Affective Disorders (2018)
Studerus, E., Gamma, A., Vollenweider, F. X. · PLOS ONE (2010)
Your Personal Research Library
Go Pro to save papers, add notes, rate studies, and organize your research into custom shelves.