Abstract
Near-death experiences (NDEs) are episodes of disconnected consciousness that typically occur in situations that involve an actual or potential physical threat or are perceived as such, and the experiences are characterized by a rich content with prototypical mystical features. Several explanatory theories for NDEs have been proposed, ranging from psychological or neurophysiological to evolutionary models. However, these concepts were often formulated independently, and, owing to the fragmented nature of research in this domain, integration of these ideas has been limited. Lines of empirical evidence from different areas of neuroscience, including non-human studies, studies investigating psychedelic-induced mystical experiences in humans, and research on the dying brain, are now converging to provide a comprehensive explanation for NDEs. In this Review, we discuss processes that might underlie the rich conscious experience in NDEs, mostly focusing on prototypical examples and addressing both the potential psychological mechanisms and neurophysiological changes, including cellular and electrophysiological brain network modifications and alterations in neurotransmitter release. On the basis of this discussion, we propose a model for NDEs that encompasses a cascade of concomitant psychological and neurophysiological processes within an evolutionary framework. We also consider how NDE research can inform the debate on the emergence of consciousness in near-death conditions that arise before brain death.
Key points
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The emergence of a rich phenomenology in near-death experiences (NDEs) during acute physiological crises might be attributed to a cascade of concomitant neurophysiological and psychological processes, including phylogenetically preserved threat responses.
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From a neurophysiological perspective, NDEs can result from impaired cerebral blood flow causing systemic hypotension, hypoxia and hypercapnia resulting in acidosis, and from increased neuronal excitability causing dysregulation of key neurotransmitter systems.
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From a psychological perspective, NDEs might be partially shaped by top–down processes and facilitated by non-pathological cognitive traits such as dissociation propensity.
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The evolutionary roots of NDEs are thought to be linked to survival and coping mechanisms, with serotonin probably mediating calming effects through 5-HT1A receptors and contributing to hallucinogenic aspects through 5-HT2A receptor hyperactivation.
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Understanding the slow recovery of brain activity after resuscitation might provide a valuable opportunity to explore the neural correlates of NDEs.
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Change history
12 June 2025
A Correction to this paper has been published: https://doi.org/10.1038/s41582-025-01111-9
References
Heim, A. Jahrbuch des Schweizer Alpenclub / 27 Notizen über den Tod durch Absturz (Verlag der Expedition des Jahrbuchs des S.A.C., 1892).
Moody, R. Life After Life (Bantam, 1975).
Hou, Y., Huang, Q., Prakash, R. & Chaudhury, S. Infrequent near-death experiences in severe brain injury survivors — a quantitative and qualitative study. Ann. Indian Acad. Neurol. 16, 75 (2013).
Rousseau, A.-F. et al. Incidence of near-death experiences in patients surviving a prolonged critical illness and their long-term impact: a prospective observational study. Crit. Care 27, 76 (2023).
Greyson, B. Incidence and correlates of near-death experiences in a cardiac care unit. Gen. Hosp. Psychiatry 25, 269–276 (2003).
Klemenc-Ketis, Z., Kersnik, J. & Grmec, S. The effect of carbon dioxide on near-death experiences in out-of-hospital cardiac arrest survivors: a prospective observational study. Crit. Care 14, R56 (2010).
Parnia, S. et al. AWARE — AWAreness during resuscitation — a prospective study. Resuscitation 85, 1799–1805 (2014).
Schwaninger, J., Eisenberg, P. R., Schechtman, K. B. & Weiss, A. N. A prospective analysis of near-death experiences in cardiac arrest patients. J. Near Death Stud. 20, 215–232 (2002).
van Lommel, P., van Wees, R., Meyers, V. & Elfferich, I. Near-death experience in survivors of cardiac arrest: a prospective study in the Netherlands. Lancet 358, 2039–2045 (2001).
Parnia, S. et al. AWAreness during REsuscitation — II: a multi-center study of consciousness and awareness in cardiac arrest. Resuscitation 191, 109903 (2023).
Mauduit, M. et al. Does hypothermic circulatory arrest for aortic surgery trigger near-death experience? Incidence of near-death experiences after aortic surgeries performed under hypothermic circulatory arrest. Aorta 9, 76–82 (2021).
Charland-Verville, V. et al. Near-death experiences in non-life-threatening events and coma of different etiologies. Front. Hum. Neurosci. 8, 203 (2014).
Facco, E. & Agrillo, C. Near-death-like experiences without life-threatening conditions or brain disorders: a hypothesis from a case report. Front. Psychol. 3, 490 (2012).
Kondziella, D., Dreier, J. P. & Olsen, M. H. Prevalence of near-death experiences in people with and without REM sleep intrusion. PeerJ 7, e7585 (2019).
Martial, C., Cassol, H., Laureys, S. & Gosseries, O. Near-death experience as a probe to explore (disconnected) consciousness. Trends Cogn. Sci. 24, 173–183 (2020).
Fritz, P., Lejeune, N., Cardone, P., Gosseries, O. & Martial, C. Bridging the gap: (a)typical psychedelic and near-death experience insights. Curr. Opin. Behav. Sci. 55, 101349 (2024).
Martial, C. et al. Neurochemical models of near-death experiences: a large-scale study based on the semantic similarity of written reports. Conscious. Cogn. 69, 52–69 (2019).
Timmermann, C. et al. DMT models the near-death experience. Front. Psychol. 9, 1424 (2018).
Greyson, B. Dissociation in people who have near-death experiences: out of their bodies or out of their minds? Lancet 355, 460–463 (2000).
Martial, C., Cassol, H., Charland-Verville, V., Merckelbach, H. & Laureys, S. Fantasy proneness correlates with the intensity of near-death experience. Front. Psychiatry 9, 190 (2018).
Noyes, R. & Slymen, D. J. The subjective response to life-threatening danger. OMEGA J. Death Dying 9, 313–321 (1979).
Owens, J., Cook, E. W. & Stevenson, I. Features of ‘near-death experience’ in relation to whether or not patients were near death. Lancet 336, 1175–1177 (1990).
Blackmore, S. J. & Troscianko, T. S. The physiology of the tunnel. J. Near Death Stud. 8, 15–28 (1989).
Blanke, O. & Arzy, S. The out-of-body experience: disturbed self-processing at the temporo-parietal junction. Neuroscientist 11, 16–24 (2005).
Nelson, K. R., Mattingly, M., Lee, S. A. & Schmitt, F. A. Does the arousal system contribute to near death experience? Neurology 66, 1003–1009 (2006).
Raffaelli, B. et al. Near‐death experiences are associated with rapid eye movement (REM) sleep intrusions in migraine patients, independent of migraine aura. Eur. J. Neurol. 30, 3322–3331 (2023).
Peinkhofer, C., Martial, C., Cassol, H., Laureys, S. & Kondziella, D. The evolutionary origin of near-death experiences: a systematic investigation. Brain Commun. 3, fcab132 (2021).
Long, J. & Perry, P. Evidence of the Afterlife: the Science of Near-Death Experiences (HarperOne, 2010).
Van Lommel, P. Non-local consciousness a concept based on scientific research on near-death experiences during cardiac arrest. J. Conscious. Stud. 20, 7–48 (2013).
Zeman, A. What in the world is consciousness? Prog. Brain Res. 150, 1–10 (2005).
Li, D. et al. Asphyxia-activated corticocardiac signaling accelerates onset of cardiac arrest. Proc. Natl Acad. Sci. USA 112, E2073–E2082 (2015).
Kandel, E. R. A new intellectual framework for psychiatry. Am. J. Psychiatry 155, 457–469 (1998).
Sergent, C. & Naccache, L. Imaging neural signatures of consciousness: ‘what’, ‘when’, ‘where’ and ‘how’ does it work? Arch. Ital. Biol. 91, 106 (2012).
Tononi, G. Consciousness, information integration, and the brain. Prog. Brain Res. 150, 109–126 (2005).
Koch, C., Massimini, M., Boly, M. & Tononi, G. Neural correlates of consciousness: progress and problems. Nat. Rev. Neurosci. 17, 307–321 (2016).
Martial, C. et al. The Near-Death Experience Content (NDE-C) scale: development and psychometric validation. Conscious. Cogn. 86, 103049 (2020).
Whinnery, J. E. & Whinnery, A. M. Acceleration-induced loss of consciousness. A review of 500 episodes. Arch. Neurol. 47, 764–776 (1990).
Annen, J. et al. Mapping the functional brain state of a world champion freediver in static dry apnea. Brain Struct. Funct. 226, 2675–2688 (2021).
Lempert, T., Bauer, M. & Schmidt, D. Syncope: a videometric analysis of 56 episodes of transient cerebral hypoxia. Ann. Neurol. 36, 233–237 (1994).
Lempert, T., Bauer, M. & Schmidt, D. Syncope and near-death experience. Lancet 344, 829–830 (1994).
Martial, C. et al. EEG signature of near-death-like experiences during syncope-induced periods of unresponsiveness. Neuroimage 298, 120759 (2024).
Pausescu, E., Lugojan, R. & Pausescu, M. Cerebral catecholamine and serotonin metabolism in post-hypothermic brain oedema. Brain 93, 31–36 (1970).
Javaheri, S., De Hemptinne, A., Vanheel, B. & Leusen, I. Changes in brain ECF pH during metabolic acidosis and alkalosis: a microelectrode study. J. Appl. Physiol. 55, 1849–1853 (1983).
Hansen, A. J. Effect of anoxia on ion distribution in the brain. Physiol. Rev. 65, 101–148 (1985).
Charnay, Y. & Léger, L. Brain serotonergic circuitries. Dialogues Clin. Neurosci. 12, 471–487 (2010).
Mathias, A. P., Ross, D. M. & Schachter, M. Identification and distribution of 5-hydroxytryptamine in a sea anemone. Nature 180, 658–659 (1957).
Ishihara, A. et al. The tryptophan pathway is involved in the defense responses of rice against pathogenic infection via serotonin production. Plant J. 54, 481–495 (2008).
Araneda, R. & Andrade, R. 5-Hydroxytryptamine2 and 5-hydroxytryptamine1A receptors mediate opposing responses on membrane excitability in rat association cortex. Neuroscience 40, 399–412 (1991).
Whitaker-Azmitia, P. M. Serotonin and brain development: role in human developmental diseases. Brain Res. Bull. 56, 479–485 (2001).
Fletcher, P. J., Tampakeras, M., Sinyard, J. & Higgins, G. A. Opposing effects of 5-HT2A and 5-HT2C receptor antagonists in the rat and mouse on premature responding in the five-choice serial reaction time test. Psychopharmacology 195, 223–234 (2007).
Varnäs, K., Halldin, C. & Hall, H. Autoradiographic distribution of serotonin transporters and receptor subtypes in human brain. Hum. Brain Mapp. 22, 246–260 (2004).
Miyazaki, K., Miyazaki, K. W. & Doya, K. The role of serotonin in the regulation of patience and impulsivity. Mol. Neurobiol. 45, 213–224 (2012).
Miyazaki, K. W. et al. Optogenetic activation of dorsal raphe serotonin neurons enhances patience for future rewards. Curr. Biol. 24, 2033–2040 (2014).
Carhart-Harris, R. L. & Nutt, D. J. Serotonin and brain function: a tale of two receptors. J. Psychopharmacol. 31, 1091–1120 (2017).
Gerstl, F. et al. Multimodal imaging of human early visual cortex by combining functional and molecular measurements with fMRI and PET. Neuroimage 41, 204–211 (2008).
Kometer, M., Schmidt, A., Jancke, L. & Vollenweider, F. X. Activation of serotonin 2A receptors underlies the psilocybin-induced effects on oscillations, N170 visual-evoked potentials, and visual hallucinations. J. Neurosci. 33, 10544–10551 (2013).
William Moreau, A., Amar, M., Le Roux, N., Morel, N. & Fossier, P. Serotoninergic fine-tuning of the excitation–inhibition balance in rat visual cortical networks. Cereb. Cortex 20, 456–467 (2010).
González-Maeso, J. et al. Identification of a serotonin/glutamate receptor complex implicated in psychosis. Nature 452, 93–97 (2008).
Huot, P. et al. Increased 5‐HT2A receptors in the temporal cortex of parkinsonian patients with visual hallucinations. Mov. Disord. 25, 1399–1408 (2010).
Griffiths, R., Richards, W., Johnson, M., McCann, U. & Jesse, R. Mystical-type experiences occasioned by psilocybin mediate the attribution of personal meaning and spiritual significance 14 months later. J. Psychopharmacol. 22, 621–632 (2008).
Vollenweider, F. X. & Kometer, M. The neurobiology of psychedelic drugs: implications for the treatment of mood disorders. Nat. Rev. Neurosci. 11, 642–651 (2010).
Carhart-Harris, R. L. et al. Neural correlates of the psychedelic state as determined by fMRI studies with psilocybin. Proc. Natl Acad. Sci. USA 109, 2138–2143 (2012).
Tagliazucchi, E. et al. Increased global functional connectivity correlates with LSD-induced ego dissolution. Curr. Biol. 26, 1043–1050 (2016).
De Ridder, D., Van Laere, K., Dupont, P., Menovsky, T. & Van de Heyning, P. Visualizing out-of-body experience in the brain. N. Engl. J. Med. 357, 1829–1833 (2007).
Arzy, S., Thut, G., Mohr, C., Michel, C. M. & Blanke, O. Neural basis of embodiment: distinct contributions of temporoparietal junction and extrastriate body area. J. Neurosci. 26, 8074–8081 (2006).
Arzy, S., Seeck, M., Ortigue, S., Spinelli, L. & Blanke, O. Induction of an illusory shadow person. Nature 443, 287 (2006).
Strassman, R. DMT: the Spirit Molecule: a Doctor’s Revolutionary Research into the Biology of Near-Death and Mystical Experiences (Park Street, 2001).
Michael, P., Luke, D. & Robinson, O. This is your brain on death: a comparative analysis of a near-death experience and subsequent 5-methoxy-DMT experience. Front. Psychol. 14, 1083361 (2023).
Peroutka, S. J. & Howell, T. A. The molecular evolution of G protein-coupled receptors: focus on 5-hydroxytryptamine receptors. Neuropharmacology 33, 319–324 (1994).
Barnes, N. M. & Sharp, T. A review of central 5-HT receptors and their function. Neuropharmacology 38, 1083–1152 (1999).
Brouwer, A. & Carhart-Harris, R. L. Pivotal mental states. J. Psychopharmacol. 35, 319–352 (2021).
Wutzler, A., Mavrogiorgou, P., Winter, C. & Juckel, G. Elevation of brain serotonin during dying. Neurosci. Lett. 498, 20–21 (2011).
Meldrum, B. S. Glutamate as a neurotransmitter in the brain: review of physiology and pathology. J. Nutr. 130, 1007S–1015S (2000).
Edmonds, B., Gibb, A. J. & Colquhoun, D. Mechanisms of activation of glutamate receptors and the time course of excitatory synaptic currents. Annu. Rev. Physiol. 57, 495–519 (1995).
Traynelis, S. F. et al. Glutamate receptor ion channels: structure, regulation, and function. Pharmacol. Rev. 62, 405–496 (2010).
Godaux, E. Les Neurones, Les Synapses et Les Fibres Musculaires (Editions Masson, 1997).
Tabone, C. J. & Ramaswami, M. Is NMDA receptor-coincidence detection required for learning and memory? Neuron 74, 767–769 (2012).
Paulsen, O. & Sejnowski, T. J. Natural patterns of activity and long-term synaptic plasticity. Curr. Opin. Neurobiol. 10, 172–179 (2000).
Dingledine, R. N-Methyl aspartate activates voltage-dependent calcium conductance in rat hippocampal pyramidal cells. J. Physiol. 343, 385–405 (1983).
Bliss, T. V. & Collingridge, G. L. A synaptic model of memory: long-term potentiation in the hippocampus. Nature 361, 31–39 (1993).
Corazza, O. & Schifano, F. Near-death states reported in a sample of 50 misusers. Subst. Use Misuse 45, 916–924 (2010).
Jansen, K. Near death experience and the NMDA receptor. BMJ 298, 1708 (1989).
Jansen, K. L. R. The ketamine model of the near-death experience: a central role for the N-methyl-D-aspartate receptor. J. Near Death Stud. 16, 5–26 (1997).
Collingridge, G. L., Kehl, S. J. & McLennan, H. Excitatory amino acids in synaptic transmission in the Schaffer collateral-commissural pathway of the rat hippocampus. J. Physiol. 334, 33–46 (1983).
Elston, G. N. Cortex, cognition and the cell: new insights into the pyramidal neuron and prefrontal function. Cereb. Cortex 13, 1124–1138 (2003).
Adell, A. Brain NMDA receptors in schizophrenia and depression. Biomolecules 10, 947 (2020).
Haaf, M., Leicht, G., Curic, S. & Mulert, C. Glutamatergic deficits in schizophrenia — biomarkers and pharmacological interventions within the ketamine model. Curr. Pharm. Biotechnol. 19, 293–307 (2018).
Halstead, J. M. et al. Translation. An RNA biosensor for imaging the first round of translation from single cells to living animals. Science 347, 1367–1671 (2015).
Höflich, A. et al. Ketamine-dependent neuronal activation in healthy volunteers. Brain Struct. Funct. 222, 1533–1542 (2017).
Hussain, L. S., Reddy, V. & Maani, C. V. Physiology, noradrenergic synapse. StatPearls (StatPearls, 2023).
Borovsky, V., Herman, M., Dunphy, G., Caplea, A. & Ely, D. CO2 asphyxia increases plasma norepinephrine in rats via sympathetic nerves. Am. J. Physiol. 274, R19–R22 (1998).
Reiner, P. B. Correlational analysis of central noradrenergic neuronal activity and sympathetic tone in behaving cats. Brain Res. 378, 86–96 (1986).
Poe, G. R. et al. Locus coeruleus: a new look at the blue spot. Nat. Rev. Neurosci. 21, 644–659 (2020).
Aston-Jones, G., Rajkowski, J. & Cohen, J. Locus coeruleus and regulation of behavioral flexibility and attention. Prog. Brain Res. 126, 165–182 (2000).
Murchison, C. F. et al. A distinct role for norepinephrine in memory retrieval. Cell 117, 131–143 (2004).
Cahill, L. & Alkire, M. T. Epinephrine enhancement of human memory consolidation: interaction with arousal at encoding. Neurobiol. Learn. Mem. 79, 194–198 (2003).
LaLumiere, R. T., McGaugh, J. L. & McIntyre, C. K. Emotional modulation of learning and memory: pharmacological implications. Pharmacol. Rev. 69, 236–255 (2017).
Tully, K., Li, Y., Tsvetkov, E. & Bolshakov, V. Y. Norepinephrine enables the induction of associative long-term potentiation at thalamo-amygdala synapses. Proc. Natl Acad. Sci. USA 104, 14146–14150 (2007).
Timofeev, I. & Steriade, M. Low-frequency rhythms in the thalamus of intact-cortex and decorticated cats. J. Neurophysiol. 76, 4152–4168 (1996).
Ramadan, W., Eschenko, O. & Sara, S. J. Hippocampal sharp wave/ripples during sleep for consolidation of associative memory. PLoS ONE 4, e6697 (2009).
McGaugh, J. L. The amygdala modulates the consolidation of memories of emotionally arousing experiences. Annu. Rev. Neurosci. 27, 1–28 (2004).
Martial, C. et al. Intensity and memory characteristics of near-death experiences. Conscious. Cogn. 56, 120–127 (2017).
Thonnard, M. et al. Characteristics of near-death experiences memories as compared to real and imagined events memories. PLoS ONE 8, e57620 (2013).
Hasselmo, M. E. The role of acetylcholine in learning and memory. Curr. Opin. Neurobiol. 16, 710–715 (2006).
French, I. T. & Muthusamy, K. A. A review of the pedunculopontine nucleus in Parkinson’s disease. Front. Aging Neurosci. 10, 99 (2018).
Lew, C. H. & Semendeferi, K. in Evolution of Nervous Systems (ed. Kaas, J. H.) 277–291 (Elsevier, 2017).
Oswald, M. J. et al. Cholinergic basal forebrain nucleus of Meynert regulates chronic pain-like behavior via modulation of the prelimbic cortex. Nat. Commun. 13, 5014 (2022).
Ziemann, A. E. et al. The amygdala is a chemosensor that detects carbon dioxide and acidosis to elicit fear behavior. Cell 139, 1012–1021 (2009).
Sotelo, J., Perez, R., Cuevara, P. & Fernandez, A. Changes in brain, plasma and cerebrospinal fluid contents of β-endorphin in dogs at the moment of death. Neurol. Res. 17, 223–225 (1995).
Kanchan, T., Rastogi, P. & Mohanty, M. Profile of near drowning victims in a coastal region of Karnataka. J. Indian Acad. Forensic Sci. 29, 52–54 (2007).
Morse, M. A near-death experience in a 7-year-old child. Arch. Pediatr. Adolesc. Med. 137, 959 (1983).
Blackmore, S. J. Near-death experiences. J. R. Soc. Med. 89, 73–76 (1996).
Bartels, A. & Zeki, S. The neural correlates of maternal and romantic love. Neuroimage 21, 1155–1166 (2004).
Craig, A. D. (Bud). Forebrain emotional asymmetry: a neuroanatomical basis? Trends Cogn. Sci. 9, 566–571 (2005).
Leibenluft, E., Gobbini, M. I., Harrison, T. & Haxby, J. V. Mothers’ neural activation in response to pictures of their children and other children. Biol. Psychiatry 56, 225–232 (2004).
Martial, C., Charland-Verville, V., Dehon, H. & Laureys, S. False memory susceptibility in coma survivors with and without a near-death experience. Psychol. Res. 82, 806–818 (2018).
Kapur, S. Psychosis as a state of aberrant salience: a framework linking biology, phenomenology, and pharmacology in schizophrenia. Am. J. Psychiatry 160, 13–23 (2003).
Preller, K. H. et al. The fabric of meaning and subjective effects in LSD-induced states depend on serotonin 2A receptor activation. Curr. Biol. 27, 451–457 (2017).
Creese, I., Burt, D. R. & Snyder, S. H. Dopamine receptor binding: differentiation of agonist and antagonist states with 3H-dopamine and 3H-haloperidol. Life Sci. 17, 993–1001 (1975).
Vollenweider, F. X., Vollenweider-Scherpenhuyzen, M. F. I., Bäbler, A., Vogel, H. & Hell, D. Psilocybin induces schizophrenia-like psychosis in humans via a serotonin-2 agonist action. Neuroreport 9, 3897–3902 (1998).
Lutz, P. L., Nilsson, G. E. & Prentice, H. M. The Brain Without Oxygen: Causes of Failure-Physiological and Molecular Mechanisms for Survival (Kluwer Academic, 2002).
Martial, C., Fritz, P., Lejeune, N. & Gosseries, O. Exploring awareness in cardiac arrest studies: methodological challenges. Resuscitation 194, 109980 (2024).
Greyson, B. Implications of near-death experiences for a postmaterialist psychology. Psychol. Relig. Spiritual. 2, 37 (2010).
Bartolomei, F. et al. The role of the dorsal anterior insula in ecstatic sensation revealed by direct electrical brain stimulation. Brain Stimul. 12, 1121–1126 (2019).
Picard, F. & Friston, K. Predictions, perception, and a sense of self. Neurology 83, 1112–1118 (2014).
Arzy, S., Idel, M., Landis, T. & Blanke, O. Why revelations have occurred on mountains? Linking mystical experiences and cognitive neuroscience. Med. Hypotheses 65, 841–845 (2005).
Burtscher, J. & Schwarzer, C. The opioid system in temporal lobe epilepsy: functional role and therapeutic potential. Front. Mol. Neurosci. 10, 245 (2017).
Landtblom, A.-M. The “sensed presence”: an epileptic aura with religious overtones. Epilepsy Behav. 9, 186–188 (2006).
Sacks, O. Seeing God in the third millennium. How the brain creates out-of-body experiences and religious epiphanies. The Atlantic https://www.theatlantic.com/health/archive/2012/12/seeing-god-in-the-third-millennium/266134/ (2012).
Britton, W. B. & Bootzin, R. R. Near-death experiences and the temporal lobe. Psychol. Sci. 15, 254–258 (2004).
Leung, L. C. et al. Neural signatures of sleep in zebrafish. Nature 571, 198–204 (2019).
Scammell, T. E., Arrigoni, E. & Lipton, J. O. Neural circuitry of wakefulness and sleep. Neuron 93, 747–765 (2017).
Yamazaki, R. et al. Evolutionary origin of distinct NREM and REM sleep. Front. Psychol. 11, 567618 (2020).
Peever, J. & Fuller, P. M. The biology of REM sleep. Curr. Biol. 27, R1237–R1248 (2017).
Ohayon, M. M., Priest, R. G., Zulley, J., Smirne, S. & Paiva, T. Prevalence of narcolepsy symptomatology and diagnosis in the European general population. Neurology 58, 1826–1833 (2002).
Kondziella, D., Olsen, M. H., Lemale, C. L. & Dreier, J. P. Migraine aura, a predictor of near-death experiences in a crowdsourced study. PeerJ 7, e8202 (2019).
Lu, J., Sherman, D., Devor, M. & Saper, C. B. A putative flip-flop switch for control of REM sleep. Nature 441, 589–594 (2006).
Nelson, K. R., Mattingly, M. & Schmitt, F. A. Out-of-body experience and arousal. Neurology 68, 794–795 (2007).
Mahowald, M. W. & Schenck, C. H. Dissociated states of wakefulness and sleep. Neurology 42, 44–51 (1992).
Maquet, P. et al. Human cognition during REM sleep and the activity profile within frontal and parietal cortices: a reappraisal of functional neuroimaging data. Prog. Brain Res. 150, 219–227 (2005).
Blanke, O., Ortigue, S., Landis, T. & Seeck, M. Stimulating illusory own-body perceptions. Nature 419, 269–270 (2002).
Vagg, D. J., Bandler, R. & Keay, K. A. Hypovolemic shock: critical involvement of a projection from the ventrolateral periaqueductal gray to the caudal midline medulla. Neuroscience 152, 1099–1109 (2008).
Nicol, A. U. & Morton, A. J. Characteristic patterns of EEG oscillations in sheep (Ovis aries) induced by ketamine may explain the psychotropic effects seen in humans. Sci. Rep. 10, 9440 (2020).
Frohlich, J., Toker, D. & Monti, M. M. Consciousness among delta waves: a paradox? Brain J. Neurol. 144, 2257–2277 (2021).
Vijayan, S., Lepage, K. Q., Kopell, N. J. & Cash, S. S. Frontal beta-theta network during REM sleep. eLife 6, e18894 (2017).
Timmermann, C. et al. Neural correlates of the DMT experience assessed with multivariate EEG. Sci. Rep. 9, 16324 (2019).
Lee, U. et al. Disruption of frontal–parietal communication by ketamine, propofol, and sevoflurane. Anesthesiology 118, 1264–1275 (2013).
Sarasso, S. et al. Consciousness and complexity during unresponsiveness induced by propofol, xenon, and ketamine. Curr. Biol. 25, 3099–3105 (2015).
Vlisides, P. E. et al. Neurophysiologic correlates of ketamine sedation and anesthesia. Anesthesiology 127, 58–69 (2017).
Vlisides, P. E. et al. Subanaesthetic ketamine and altered states of consciousness in humans. Br. J. Anaesth. 121, 249–259 (2018).
Carhart-Harris, R. L. The entropic brain — revisited. Neuropharmacology 142, 167–178 (2018).
Greyson, B. The near-death experience as a focus of clinical attention. J. Nerv. Ment. Dis. 185, 327–334 (1997).
Noyes, R. & Kletti, R. Depersonalization in the face of life-threatening danger: a description. Psychiatry 39, 19–27 (1976).
Noyes, R. Jr & Kletti, R. Depersonalization in response to life-threatening danger. Compr. Psychiatry 18, 375–384 (1977).
Chawla, L. S., Akst, S., Junker, C., Jacobs, B. & Seneff, M. G. Surges of electroencephalogram activity at the time of death: a case series. J. Palliat. Med. 12, 1095–1100 (2009).
Borjigin, J. et al. Surge of neurophysiological coherence and connectivity in the dying brain. Proc. Natl Acad. Sci. USA 110, 14432–14437 (2013).
Bland, N. S., Mattingley, J. B. & Sale, M. V. Gamma coherence mediates interhemispheric integration during multiple object tracking. J. Neurophysiol. 123, 1630–1644 (2020).
Cho, K. K. A. et al. Cross-hemispheric gamma synchrony between prefrontal parvalbumin interneurons supports behavioral adaptation during rule shift learning. Nat. Neurosci. 23, 892–902 (2020).
Ghosh, M. et al. Running speed and REM sleep control two distinct modes of rapid interhemispheric communication. Cell Rep. 40, 111028 (2022).
Lee, D. E. et al. Neural correlates of consciousness at near-electrocerebral silence in an asphyxial cardiac arrest model. Brain Connect. 7, 172–181 (2017).
Vicente, R. et al. Enhanced interplay of neuronal coherence and coupling in the dying human brain. Front. Aging Neurosci. 14, 813531 (2022).
Xu, G. et al. Surge of neurophysiological coupling and connectivity of gamma oscillations in the dying human brain. Proc. Natl Acad. Sci. USA 120, e2216268120 (2023).
Seth, A. K. & Bayne, T. Theories of consciousness. Nat. Rev. Neurosci. 23, 439–452 (2022).
Mena-Segovia, J., Sims, H. M., Magill, P. J. & Bolam, J. P. Cholinergic brainstem neurons modulate cortical gamma activity during slow oscillations. J. Physiol. 586, 2947–2960 (2008).
Urbano, F. J. et al. Pedunculopontine nucleus gamma band activity — preconscious awareness, waking, and REM sleep. Front. Neurol. 5, 210 (2014).
Llinás, R. & Ribary, U. Coherent 40-Hz oscillation characterizes dream state in humans. Proc. Natl Acad. Sci. USA 90, 2078–2081 (1993).
Boly, M. et al. Are the neural correlates of consciousness in the front or in the back of the cerebral cortex? Clinical and neuroimaging evidence. J. Neurosci. 37, 9603–9613 (2017).
Wittling, W., Block, A., Schweiger, E. & Genzel, S. Hemisphere asymmetry in sympathetic control of the human myocardium. Brain Cogn. 38, 17–35 (1998).
Ammermann, H. et al. MRI brain lesion patterns in patients in anoxia-induced vegetative state. J. Neurol. Sci. 260, 65–70 (2007).
Els, T., Kassubek, J., Kubalek, R. & Klisch, J. Diffusion-weighted MRI during early global cerebral hypoxia: a predictor for clinical outcome? Acta Neurol. Scand. 110, 361–367 (2004).
Holden, J. M. & Loseu, S. Shedding light on the tunnel and light in near-death experiences: a case study. J. Near Death Stud. 34, 27–43 (2015).
Greyson, B. Near-death experience: clinical implications. Arch. Clin. Psychiatry 34, 116–125 (2007).
Chawla, L. S. et al. Characterization of end-of-life electroencephalographic surges in critically ill patients. Death Stud. 41, 385–392 (2017).
Schramm, A. E. et al. Identifying neuronal correlates of dying and resuscitation in a model of reversible brain anoxia. Prog. Neurobiol. 185, 101733 (2020).
Nahm, M., Greyson, B., Kelly, E. W. & Haraldsson, E. Terminal lucidity: a review and a case collection. Arch. Gerontol. Geriatr. 55, 138–142 (2012).
Morse, M. L., Venecia, D. & Milstein, J. Near-death experiences: a neurophysiologic explanatory model. J. Near Death Stud. 8, 45–53 (1989).
Blanke, O., Landis, T., Spinelli, L. & Seeck, M. Out-of-body experience and autoscopy of neurological origin. Brain J. Neurol. 127, 243–258 (2004).
Blanke, O. & Metzinger, T. Full-body illusions and minimal phenomenal selfhood. Trends Cogn. Sci. 13, 7–13 (2009).
Potts, M. The evidential value of near-death experiences for belief in life after death. J. Near Death Stud. 20, 233–258 (2002).
Schwartz, J. M., Stapp, H. P. & Beauregard, M. Quantum physics in neuroscience and psychology: a neurophysical model of mind–brain interaction. Philos. Trans. R. Soc. B Biol. Sci. 360, 1309–1327 (2005).
van Lommel, P. About the continuity of our consciousness. Adv. Exp. Med. Biol. 550, 115–132 (2004).
Parnia, S. Do reports of consciousness during cardiac arrest hold the key to discovering the nature of consciousness? Med. Hypotheses 69, 933–937 (2007).
Martial, C., Gosseries, O., Cassol, H. & Kondziella, D. Studying death and near-death experiences requires neuroscientific expertise. Ann. N. Y. Acad. Sci. 1517, 11–14 (2022).
Vanhaudenhuyse, A., Thonnard, M. & Laureys, S. in Yearbook of Intensive Care and Emergency Medicine 2009 (ed. Vincent, J.-L.) 961–968 (2009).
Barker, S. A., McIlhenny, E. H. & Strassman, R. A critical review of reports of endogenous psychedelic N,N‐dimethyltryptamines in humans: 1955–2010. Drug Test. Anal. 4, 617–635 (2012).
Barker, S. A., Borjigin, J., Lomnicka, I. & Strassman, R. LC/MS/MS analysis of the endogenous dimethyltryptamine hallucinogens, their precursors, and major metabolites in rat pineal gland microdialysate. Biomed. Chromatogr. 27, 1690–1700 (2013).
Beaton, J. M. & Morris, P. E. Ontogeny of N,N-dimethyltryptamine and related indolealkylamine levels in neonatal rats. Mech. Ageing Dev. 25, 343–347 (1984).
Dean, J. G. et al. Biosynthesis and extracellular concentrations of N,N-dimethyltryptamine (DMT) in mammalian brain. Sci. Rep. 9, 9333 (2019).
Franzen, F. & Gross, H. Tryptamine, N,N-dimethyltryptamine, N,N-dimethyl-5-hydroxytryptamine and 5-methoxytryptamine in human blood and urine. Nature 206, 1052 (1965).
Kärkkäinen, J. et al. Potentially hallucinogenic 5‐hydroxytryptamine receptor ligands bufotenine and dimethyltryptamine in blood and tissues. Scand. J. Clin. Lab. Invest. 65, 189–199 (2005).
Nichols, D. E. N. N-Dimethyltryptamine and the pineal gland: separating fact from myth. J. Psychopharmacol. 32, 30–36 (2018).
Glynos, N. G. et al. Neurochemical and neurophysiological effects of intravenous administration of N,N-dimethyltryptamine in rats. Preprint at bioRxiv https://doi.org/10.1101/2024.04.19.589047 (2024).
Bush, N. E. & Greyson, B. Distressing near-death experiences: the basics. Mol. Med. 111, 486–490 (2014).
Cassol, H. et al. A systematic analysis of distressing near-death experience accounts. Memory 27, 1122–1129 (2019).
Greyson, B. & Evans Bush, N. Distressing near-death experiences. Psychiatry 55, 95–110 (1992).
Ring, K. Frightening near-death experiences revisited: a commentary on responses to my paper by Christopher Bache and Nancy Evans Bush. J. Near Death Stud. 13, 55–64 (1994).
Martial, C. et al. Losing the self in near-death experiences: the experience of ego-dissolution. Brain Sci. 11, 929 (2021).
Andrijevic, D. et al. Cellular recovery after prolonged warm ischaemia of the whole body. Nature 608, 405–412 (2022).
Vrselja, Z. et al. Restoration of brain circulation and cellular functions hours post-mortem. Nature 568, 336–343 (2019).
Joffe, A. R. Should the criterion for brain death require irreversible or permanent cessation of function? Irreversible: the UDDA revision series. Neurology 101, 181–183 (2023).
Acknowledgements
The authors are grateful to A. Deward (Illumine) for conceptualizing and designing the original Figure 3 and to J. Delroisse (Zoology Laboratory, Université de Mons, Belgium) for his precious phylogenetic insights. This work was supported by the BIAL Foundation. O.G. is a research associate and N.L. is a postdoctoral specialist at Fonds de la Recherche Scientifique, Belgium.
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N.L., P.F. and C.M. conceptualized the Review, wrote the article and edited the manuscript before submission. All authors contributed substantially to the discussion of the content and reviewed and edited the manuscript before submission. All authors approved the version to be published.
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V.B. has had or continues to have financial relationships with Medtronic, Edwards Medical, Orion Pharma, Grünenthal and Elsevier. He is Deputy Editor-in-Chief of Acta Anaesthesiologica Belgica. The other authors declare no competing interests.
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Glossary
- Agonal
-
A phenomenon occurring in the final stages of life, typically associated with severe physiological distress or the process of dying.
- Atonia
-
A clinical sign characterized by a reduction in or complete loss of tone and contractility, most often referring to muscle tone.
- Aura
-
The initial symptom of a focal epileptic seizure, reflecting localized abnormal brain activity before it potentially spreads.
- Default-mode network
-
(DMN). A set of brain regions that show correlated functional activity and are typically active during the resting state.
- Dissociation
-
A psychological state in which an individual experiences a disconnection between their thoughts, sensations, memories or sense of identity.
- Ego dissolution
-
A temporary state characterized by the blurring or loss of boundaries between the self and the external world, often accompanied by disruption of self-identity.
- Entropic brain hypothesis
-
A theory suggesting that the subjective quality of a specific experience is reflected in the measurement of brain entropy (greater diversity of brain activity patterns), positing that increased complexity of brain activity correlates with an expansion in some key property of consciousness.
- Experiencers
-
People who have recalled a near-death experience.
- Glomus cell
-
Specialized cells located in the carotid and aortic bodies that act as peripheral chemoreceptors, sensing changes in blood oxygen, CO2 and pH levels and helping to regulate breathing.
- Out-of-body experiences
-
(OBEs). Subjective experiences in which the self is perceived as existing outside the boundaries of a body (disembodiment), sometimes accompanied by the perception of one’s body from an extrapersonal space (autoscopy).
- Phenomenology
-
The lived, first-person experience of reality as it is directly perceived, including sensory, emotional and cognitive elements, shaped by personal context and perspective.
- Self-representation
-
The mental process or cognitive ability by which individuals represent themselves, including their characteristics, values and role within the social and physical environment.
- Thanatosis
-
A behaviour in which an animal ‘plays dead’ by entering a state of immobility or paralysis, typically in an attempt to avoid predators.
- Vasovagal syncope
-
A common type of fainting caused by a sudden drop in heart rate and blood pressure, leading to reduced blood flow to the brain.
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Martial, C., Fritz, P., Gosseries, O. et al. A neuroscientific model of near-death experiences. Nat Rev Neurol 21, 297–311 (2025). https://doi.org/10.1038/s41582-025-01072-z
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DOI: https://doi.org/10.1038/s41582-025-01072-z
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