The DOI matches its Crossref record; 62 of the 62 references it cites were found in a registry or an index.
The Psychedelic State Induced by Ayahuasca Modulates the Activity and Connectivity of the Default Mode Network
Open accessAbstract
The experiences induced by psychedelics share a wide variety of subjective features, related to the complex changes in perception and cognition induced by this class of drugs. A remarkable increase in introspection is at the core of these altered states of consciousness. Self-oriented mental activity has been consistently linked to the Default Mode Network (DMN), a set of brain regions more active during rest than during the execution of a goal-directed task. Here we used fMRI technique to inspect the DMN during the psychedelic state induced by Ayahuasca in ten experienced subjects. Ayahuasca is a potion traditionally used by Amazonian Amerindians composed by a mixture of compounds that increase monoaminergic transmission. In particular, we examined whether Ayahuasca changes the activity and connectivity of the DMN and the connection between the DMN and the task-positive network (TPN). Ayahuasca caused a significant decrease in activity through most parts of the DMN, including its most consistent hubs: the Posterior Cingulate Cortex (PCC)/Precuneus and the medial Prefrontal Cortex (mPFC). Functional connectivity within the PCC/Precuneus decreased after Ayahuasca intake. No significant change was observed in the DMN-TPN orthogonality. Altogether, our results support the notion that the altered state of consciousness induced by Ayahuasca, like those induced by psilocybin (another serotonergic psychedelic), meditation and sleep, is linked to the modulation of the activity and the connectivity of the DMN.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Traditions of meditation and ritual use of medicinal plants, fungi, and animals with consciousness-altering capacities have similar abilities to induce trance states, although these are often used in more inward-focused settings to explore one's own body/mind and connection to the adjoining socio-ecological environment-even if practiced as a group (Millière et al. 2018; Palhano-Fontes et al. 2015;”
From Cultural Evolution of Religion, Spirituality and Ritual: Impacts On Human Cooperation (2024) · cites this paper as Palhano-Fontes et al. 2015
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“It has been demonstrated with functional magnetic resonance imaging (fMRI) that during psychedelic experience, the DMN is modulated, which sharply reduces blood flow and connection within its nodes [46], leading to decreased functional connectivity within the DMN and increased between-network connectivity [47, 48].”
From Mindfulness meditation and psychedelics: potential synergies and commonalities (2023) · cites this paper as [47]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Similarly, the administration of various psychedelic drugs has led to transient deactivation of certain DMN hubs, including the mPFC, PCC and anterior cingulate cortex (ACC) (45, 114).”
From Examining the Potential Synergistic Effects Between Mindfulness Training and Psychedelic-Assisted Therapy (2021) · cites this paper as [114]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Palhano-Fontes et al. (2015) reported decreased BOLD signal in DMN nodes including the MPFC and PCC during ayahuasca intoxication.”
From Self unbound: ego dissolution in psychedelic experience (2017) · cites this paper as Palhano-Fontes et al. 2015
The cited source says what the claim attributes to it.
In the citing paper
“A number of studies have demonstrated that classic psychedelics acutely reduce activity and internal functional connectivity within the DMN [28, 29], potentially reducing abstracted (perceptually decoupled) and self-referential rumination, a hallmark of depressotypic thinking [30–32].”
From The psychological processes of classic psychedelics in the treatment of depression: a systematic review protocol (2022) · cites this paper as [28]
In the citing paper
“Ayahuasca decreases the functional connectivity within the prefrontal cortex and in connections with other areas of the brain that are involved in a wide range of ordinary cognitive processes (Palhano-Fontes et al., 2015).”
From The therapeutic potentials of Ayahuasca: possible effects against various diseases of civilization (2016) · cites this paper as Palhano-Fontes et al., 2015
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
A default mode of brain function
Raichle, M. E., MacLeod, A. M., Snyder, A. Z., Powers, W. J., Gusnard, D. A., & Shulman, G. L. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.2.676 · Cited by 12,190
The Brain's Default Network: Anatomy, Function, and Relevance to Disease
Buckner, R. L., Andrews‐Hanna, J. R., & Schacter, D. L. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1440.011 · Cited by 9,761
A Rating Scale for Mania: Reliability, Validity and Sensitivity
Young, R. C., Biggs, J. T., Ziegler, V. E., & Meyer, D. A. (1978) · British Journal of Psychiatry · doi:10.1192/bjp.133.5.429 · Cited by 8,744
The human brain is intrinsically organized into dynamic, anticorrelated functional networks
Fox, M. D., Snyder, A. Z., Vincent, J. L., Corbetta, M., Van Essen, D. C., & Raichle, M. E. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504136102 · Cited by 8,553
The varieties of religious experience: A study in human nature.
James, W. (1902) · doi:10.1037/10004-000 · Cited by 5,204
Calamita, E., Schmid, M., Kunz, M., Ndebele-Murisa, M. R., Magadza, C. H. D., Nyambe, I., & Wehrli, B. (2019) · Figshare · doi:10.26181/6153922fe919c · Cited by 4,239
Greicius, M. D., Srivastava, G., Reiss, A. L., & Menon, V. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308627101 · Cited by 3,684
Self-referential processing in our brain—A meta-analysis of imaging studies on the self
Northoff, G., Heinzel, A., de Greck, M., Bermpohl, F., Dobrowolny, H., & Panksepp, J. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2005.12.002 · Cited by 2,792
Wandering minds: the default network and stimulus-independent thought
Mason, M. F., Norton, M. I., Van Horn, J. D., Wegner, D. M., Grafton, S. T., & Macrae, C. N. (2007) · Science · doi:10.1126/science.1131295 · Cited by 2,792
Circular analysis in systems neuroscience: the dangers of double dipping
Kriegeskorte, N., Simmons, W. K., Bellgowan, P. S. F., & Baker, C. I. (2009) · Nature Neuroscience · doi:10.1038/nn.2303 · Cited by 2,696
Flagged first, then by citations
Cited by
Sorted by citations
Items 201–300 of 452
Perkins, D., Opaleye, E. S., Bouso, J. C., Tófoli, L. F., Sarris, J. J., Schubert, V., Ruffell, S., & Šimonová, H. (2023) · Psychoactives · doi:10.3390/psychoactives2040017 · Cited by 21
Damiani, S., Fusar-Poli, L., Brondino, N., Provenzani, U., Baldwin, H., Fusar-Poli, P., & Politi, P. (2020) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2020.111068 · Cited by 18
Oña, G., Sampedro, F., Romero, S., Valle, M., Camacho, V., Migliorelli, C., Mañanas, M. Á., Antonijoan, R. M., Puntes, M., Coimbra, J., et al. (2021) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyab063 · Cited by 19
Shared functional connectome fingerprints following ritualistic ayahuasca intake
Mallaroni, P., Mason, N. L., Kloft, L., Reckweg, J. T., van Oorsouw, K. I. M., Toennes, S. W., Tolle, H. M., Amico, E., & Ramaekers, J. G. (2023) · NeuroImage · doi:10.1016/j.neuroimage.2023.120480 · Cited by 20
Ruban, A., & Kołodziej, A. (2018) · Neuropsychiatria i Neuropsychologia · doi:10.5114/nan.2018.81249 · Cited by 21
Scheidegger, M. (2021) · Springer eBooks · doi:10.1007/978-3-030-55688-4_3 · Cited by 21
fMRI Evidence for Default Mode Network Deactivation Associated with Rapid Eye Movements in Sleep
Hong, C. C.-H., Fallon, J., & Friston, K. J. (2021) · Brain Sciences · doi:10.3390/brainsci11111528 · Cited by 20
The psychedelic ritual as a technique of the self
Dupuis, D. (2022) · Hau Journal of Ethnographic Theory · doi:10.1086/719792 · Cited by 17
Mind over matter: the microbial mindscapes of psychedelics and the gut-brain axis
Caspani, G., Ruffell, S., Tsang, W., Netzband, N., Rohani-Shukla, C., Swann, J. R., & Jefferies, W. A. (2024) · Pharmacological Research · doi:10.1016/j.phrs.2024.107338 · Cited by 18
Mantas, I., Flais, I., Masarapu, Y., Ionescu, T. M., Frapard, S., Jung, F., Merre, P. L., Saarinen, M., Tiklová, K., Salmani, B. Y., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-52429-9 · Cited by 21
Ayahuasca psychedelic tested for depression
Frood, A. (2015) · Nature · doi:10.1038/nature.2015.17252 · Cited by 20
Out of the box: A psychedelic model to study the creative mind
Kuypers, K. P. C. (2018) · Medical Hypotheses · doi:10.1016/j.mehy.2018.03.010 · Cited by 21
Effects of LSD on music-evoked brain activityPreprint
Kaelen, M., Lorenz, R., Barrett, F. S., Roseman, L., Orbán, C., Santos-Ribeiro, A., Wall, M. B., Feilding, A., Nutt, D. J., Muthukumaraswamy, S. D., et al. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/153031 · Cited by 19
Neural and subjective effects of inhaled DMT in natural settingsPreprint
Pallavicini, C., Cavanna, F., Zamberlán, F., de la Fuente, L. A., Perl, Y. S., Arias, M., Romero, C., Carhart-Harris, R. L., Timmermann, C., & Tagliazucchi, E. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.19.258145 · Cited by 17
Gill, H., Puramat, P., Patel, P., Gill, B., Marks, C. A., Rodrigues, N. B., Castle, D., Cha, D. S., Mansur, R. B., Rosenblat, J. D., et al. (2022) · Psychiatry Research · doi:10.1016/j.psychres.2022.114577 · Cited by 16
Armstrong, M., Castellanos, J. P., & Christie, D. (2024) · Frontiers in Pain Research · doi:10.3389/fpain.2024.1346053 · Cited by 19
An evidence-based critical review of the mind-brain identity theory
Masi, M. (2023) · Frontiers in Psychology · doi:10.3389/fpsyg.2023.1150605 · Cited by 18
Ayahuasca: what mental health professionals need to know
dos Santos, R. D., Bouso, J., & Hallak, J. (2017) · Archives of Clinical Psychiatry (São Paulo) · doi:10.1590/0101-60830000000130 · Cited by 12
Self-citationKeppler, J. (2020) · Frontiers in Psychology · doi:10.3389/fpsyg.2019.02968 · Cited by 22
Domenico, C. M., Haggerty, D. C., Mou, X., & Ji, D. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109714 · Cited by 19
Lyon, A. (2023) · doi:10.1093/oso/9780198843757.001.0001 · Cited by 20
Scoping review on shamanistic trances practices
Marie, N., Lafon, Y., Bicego, A., Grégoire, C., Rousseaux, F., Bioy, A., Vanhaudenhuyse, A., & Gosseries, O. (2024) · BMC Complementary Medicine and Therapies · doi:10.1186/s12906-024-04678-w · Cited by 21
“Additionally, a decrease in activation of the OFC at the onset of trance perception could be the neuronal correlate marking deepness of the trance [74], akin to findings in psy-chedelic studies [95, 96].”
ResultModerators of ayahuasca’s biological antidepressant action
de Sousa, G. M., Tavares, V. D. D. O., Galvão, A. C. D. M., de Almeida, R. N., Palhano-Fontes, F., Soares, B. L., Freire, F. A. D. M., Nunes, E. A., Maia‐de‐Oliveira, J. P., Perkins, D., et al. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.1033816 · Cited by 17
Self-citationRamaekers, J. G., Mallaroni, P., Kloft, L., Reckweg, J. T., Toennes, S. W., van Oorsouw, K. I. M., & Mason, N. L. (2023) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_02003 · Cited by 16
Ayahuasca: Pharmacology, Safety, and Therapeutic Effects
SANTOS, R. G. D., & Hallak, J. E. C. (2024) · Cambridge University Press eBooks · doi:10.1017/9781009585330.005 · Cited by 20
Self-citationPsychedelics align brain activity with context
Stoliker, D., Novelli, L., Khajehnejad, M. A., Biabani, M., Greaves, M. D., Barta, T., Williams, M., Chopra, S., Bazin, O., Simonsson, O., et al. (2026) · Nature · doi:10.1038/s41586-026-10910-z · Cited by 18
QEEG studies of the acute effects of the visionary tryptamine DMT.
Acosta‐Urquidi, J. (2015) · Cosmos and history · doi:10.13140/rg.2.1.4069.4248 · Cited by 14
Natural psychedelics in the treatment of depression; a review focusing on neurotransmitters
Jahanabadi, S., Amiri, S., Karkeh-abadi, M., & Razmi, A. (2023) · Fitoterapia · doi:10.1016/j.fitote.2023.105620 · Cited by 15
Tempone-Wiltshire, J., & Matthews, F. (2023) · Journal of Psychedelic Studies · doi:10.1556/2054.2023.00275 · Cited by 19
Psychedelic Therapy: A Primer for Primary Care Clinicians—N,N-Dimethyltryptamine and Ayahuasca
Shinozuka, K., Tabaac, B. J., Arenas, A., Beutler, B. D., Cherian, K. N., Evans, V. D., Fasano, C., & Muir, O. S. (2024) · American Journal of Therapeutics · doi:10.1097/mjt.0000000000001725 · Cited by 15
Vohryzek, J., Cabral, J., Timmermann, C., Atasoy, S., Roseman, L., Nutt, D. J., Carhart-Harris, R. L., Deco, G., & Kringelbach, M. L. (2024) · National Science Review · doi:10.1093/nsr/nwae124 · Cited by 15
Brain Networks, Neurotransmitters and Psychedelics: Towards a Neurochemistry of Self-Awareness
Mograbi, D. C., Rodrigues, R. F. S., Bienemann, B., & Huntley, J. D. (2024) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-024-01353-y · Cited by 17
LSD flattens the hierarchy of directed information flow in fast whole-brain dynamics
Shinozuka, K., Tewarie, P. K. B., Luppi, A. I., Lynn, C. W., Roseman, L., Muthukumaraswamy, S. D., Nutt, D. J., Carhart-Harris, R. L., Deco, G., & Kringelbach, M. L. (2024) · Imaging Neuroscience · doi:10.1162/imag_a_00420 · Cited by 16
McCulloch, D., Knudsen, G., Barrett, F., Doss, M. K., Carhart-Harris, R. L., Rosas, F., Deco, G., Kringelbach, M., Preller, K., Ramaekers, J., et al. (2021) · Neuroscience and Biobehavioral Reviews · doi:10.31234/osf.io/64kyg · Cited by 106
Müller, M. R., Ortega, F., & Hernáez, Á. M. (2022) · Anthropology and Medicine · doi:10.1080/13648470.2022.2144131 · Cited by 13
Psychedelic-Assisted Psychotherapy and Mindfulness-Based Cognitive Therapy: Potential Synergies
Chambers, R., Stoliker, D., & Simonsson, O. (2023) · Mindfulness · doi:10.1007/s12671-023-02206-4 · Cited by 14
Present and future of metabolic and metabolomics studies focused on classical psychedelics in humans
Madrid-Gambín, F., Fabregat‐Safont, D., Gomez‐Gómez, À., Olesti, E., Mason, N. L., Ramaekers, J. G., & Pozo, Ó. J. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115775 · Cited by 14
Sanchez, T. A., Ramos, L. R., Araujo, F., Schenberg, E. E., Yonamine, M., Lobo, I., de Araújo, D. B., & Luna, L. E. (2023) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2023.117430 · Cited by 14
Full Neurological Recovery From Escherichia coli Meningitis Associated With Near-Death Experience
Khanna, S., Moore, L. E., & Greyson, B. (2018) · The Journal of Nervous and Mental Disease · doi:10.1097/nmd.0000000000000874 · Cited by 13
A potential role for psilocybin in the treatment of obsessive-compulsive disorder
Jacobs, E. (2020) · Journal of Psychedelic Studies · doi:10.1556/2054.2020.00128 · Cited by 17
Psychedelic Microdosing, Mindfulness, and Anxiety: A Cross-Sectional Mediation Study
Hartong, V., & van Emmerik, A. (2023) · Journal of Psychoactive Drugs · doi:10.1080/02791072.2022.2080616 · Cited by 11
“Both psychedelic states and MM have been associated with acute changes in DMN activity and functional connectivity (CarhartHarris et al. 2012; Fox et al. 2016; Palhano-Fontes et al. 2015).”
BackgroundPsychedelic medicines for mood disorders: current evidence and clinical considerations.
Sarris, J. J., Rubiano, D. P., Day, K., Coelho, N. L. G., & Perkins, D. (2022) · PubMed · doi:10.1097/yco.0000000000000759 · Cited by 12
Acute Effects of Hallucinogens on Functional Connectivity: Psilocybin and Salvinorin-A
Bagdasarian, F. A., Hansen, H. D., Chen, J. E., Yoo, C., Placzek, M. S., Hooker, J. M., & Wey, H. (2024) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.4c00245 · Cited by 15
Tabibnia, G., Ghahremani, D. G., Pochon, J.-B. F., Diaz, M. P., & London, E. D. (2023) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2023.109919 · Cited by 13
Johansen, L., Liknaitzky, P., Nedeljkovic, M., Mastin-Purcell, L., & Murray, G. (2022) · Systematic Reviews · doi:10.1186/s13643-022-01930-7 · Cited by 11
“There is some evidence to suggest that the psychedelic state produces co-activation between the DMN and task positive networks (a network of brain regions which activate during attention demanding tasks), two networks which are usually anti-correlated [35].”
BackgroundInfluentialClassic psychedelics: the special role of the visual system
Császár-Nagy, N., Kapócs, G., & Bókkon, I. (2019) · Reviews in the Neurosciences · doi:10.1515/revneuro-2018-0092 · Cited by 12
Daldegan‐Bueno, D., Favaro, V. M., Morais, P. R., Sussulini, A., & Oliveira, M. G. M. (2022) · Behavioural Brain Research · doi:10.1016/j.bbr.2022.113878 · Cited by 11
Recent Evidence on the Antidepressant Effects of Ayahuasca
Palhano-Fontes, F., Mota-Rolim, S. A., Soares, B. L., Coelho, N. L. G., Maia‐de‐Oliveira, J. P., & de Araújo, D. B. (2021) · Springer eBooks · doi:10.1007/978-3-030-55688-4_2 · Cited by 12
Self-citationBright, S. J., & Williams, M. L. (2018) · Australian Psychologist · doi:10.1111/ap.12345 · Cited by 12
Therapeutic potential of psychedelics: History, advancements, and unexplored frontiers
Maia, J. M., de Oliveira, B. S. A., Branco, L. G. S., & Soriano, R. N. (2024) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2024.110951 · Cited by 11
Effect of LSD and music on the time-varying brain dynamics
Adamska-Stolarczyk, I., & Finc, K. (2023) · Psychopharmacology · doi:10.1007/s00213-023-06394-8 · Cited by 12
Rossi, G. N., Crevelin, E. J., Silveira, G. D. O., Queiroz, M. E. C., Yonamine, M., Hallak, J. E. C., & SANTOS, R. G. D. (2019) · Journal of Psychedelic Studies · doi:10.1556/2054.2019.009 · Cited by 10
Self-citationThe Nonclassic Psychedelic Ibogaine Disrupts Cognitive Maps
Ivan, V. E., Tomàs‐Cuesta, D. P., Esteves, I. M., Curic, D., Mohajerani, M. H., McNaughton, B. L., Davidsen, J., & Gruber, A. J. (2023) · Biological Psychiatry Global Open Science · doi:10.1016/j.bpsgos.2023.07.008 · Cited by 8
Cuerva, K., Spirou, D., Cuerva, A., Delaquis, C. P., & Raman, J. (2024) · European Eating Disorders Review · doi:10.1002/erv.3101 · Cited by 10
Mental gravity: Modelling the embodied self on the physical environment
Kent, L. (2024) · Journal of Environmental Psychology · doi:10.1016/j.jenvp.2024.102245 · Cited by 10
Winkelman, M. (2017) · Religion · Cited by 9
Sousa, D. D. N., Azevedo, M. D. A., dos Santos, M. L., Borges, T. K. D. S., de Oliveira, D. M., & Caldas, E. D. (2025) · Metabolic Brain Disease · doi:10.1007/s11011-025-01650-6 · Cited by 10
Wong, S., Meckling, G., Fabiano, N., Lee, S., Jones, B. D. M., Shorr, R., Dargél, A., Davis, A. K., Fiedorowicz, J. G., Solmi, M., et al. (2025) · Therapeutic Advances in Psychopharmacology · doi:10.1177/20451253251372449 · Cited by 9
Psychedelics and psychological strengths
Brasher, T. J., Rosen, D., & Spinella, M. (2023) · International Journal of Wellbeing · doi:10.5502/ijw.v13i1.2325 · Cited by 10
The nature of nonduality: The epistemic implications of meditative and psychedelic experiences
Tempone-Wiltshire, J., & Matthews, F. (2024) · Anthropology of Consciousness · doi:10.1111/anoc.12233 · Cited by 12
Giovannetti, C., Loizaga-Velder, A. K., Gomez, R. C., Jaime, G. R. O., Valenzuela, T. C., Sanchez, G., Marcus, O., Agin-Liebes, G., & Rush, B. R. (2025) · Journal of Psychedelic Studies · doi:10.1556/2054.2024.00401 · Cited by 7
Wittenkeller, L. M., Gudelsky, G. A., Winhusen, T. M., & Amato, D. (2025) · British Journal of Pharmacology · doi:10.1111/bph.70181 · Cited by 7
Nasretdinov, A., Barrientos, S. A., Brys, I., Halje, P., & Petersson, P. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1175575 · Cited by 7
Sidelkivska, V., & Calabuig, P. B. (2023) · Innovation The European Journal of Social Science Research · doi:10.1080/13511610.2023.2231161 · Cited by 7
I feel your pain: higher empathy is associated with higher posterior default mode network activity
Oliva, V. N. L. D. S., Riegner, G., Dean, J. G., Khatib, L. A., Allen, A., Barrows, D., Chen, C., Fuentes, R., Jacobson, A., Lopez, C., et al. (2024) · Pain · doi:10.1097/j.pain.0000000000003434 · Cited by 7
Toward a neurophysiological foundation for altered states of consciousness
Tabatabaeian, S., & Suchy-Dicey, C. (2018) · Behavioral and Brain Sciences · doi:10.1017/s0140525x17002187 · Cited by 8
Psychedelics and Hallucinogens in Psychiatry: Finding New Pharmacological Targets
de Sousa, T. R., Rema, J., Machado, S. E. D. C., & Novais, F. (2021) · Current Topics in Medicinal Chemistry · doi:10.2174/1568026621666211201145800 · Cited by 7
Erhan, E., Külahlı, İ., Kandemir, O., Cemiloglu, R., Yigitbasi, O. G., & Cüreoğlu, S. (1996) · PubMed · Cited by 7
Cultural Evolution of Religion, Spirituality and Ritual: Impacts On Human Cooperation
McNamara, R. A. (2024) · KZfSS Kölner Zeitschrift für Soziologie und Sozialpsychologie · doi:10.1007/s11577-024-00937-3 · Cited by 6
“…have similar abilities to induce trance states, although these are often used in more inward-focused settings to explore one’s own body/mind and connection to the adjoining socio-ecological environment—even if practiced as a group (Millière et al. 2018; Palhano-Fontes et al. 2015; Krause 2018).”
Wang, Y., Chen, H., Wang, C., Liu, J., Miao, P., Wei, Y., Wu, L., Wang, X., Wang, P., Zhang, Y., et al. (2024) · NeuroImage Clinical · doi:10.1016/j.nicl.2024.103655 · Cited by 6
What fMRI studies say about the nature of the psychedelic effect: a scoping review
Beneš, M., Páleníček, T., & Horáček, J. (2025) · Frontiers in Neuroscience · doi:10.3389/fnins.2025.1606798 · Cited by 7
Psychedelika in der Psychiatrie – Entwicklungen und die Stellung in Deutschland
Herwig, U., Mertens, L. J., Rosal, S. P., Koller, G., Jungaberle, A., Borgwardt, S., & Gründer, G. (2023) · Fortschritte der Neurologie · Psychiatrie · doi:10.1055/a-1981-3152 · Cited by 7
Psychedelic-assisted Psychotherapy in 3-D: Acceptance, Connectedness, and Defensiveness
Fischman, L. G. (2023) · Neuropsychoanalysis · doi:10.1080/15294145.2023.2255991 · Cited by 6
OAV and 5D-ASC for Brazilian Portuguese: A validation and adaptation study
Rodrigues, R., Wießner, I., Daldegan‐Bueno, D., Bienemann, B., Pontual, A. A. D. D., Tófoli, L. F., & Mograbi, D. C. (2025) · Journal of Psychopharmacology · doi:10.1177/02698811251344685 · Cited by 6
Controlling extended criticality via modular connectivity
Gutjahr, N., Hövel, P., & Viol, A. (2021) · Journal of Physics Complexity · doi:10.1088/2632-072x/ac202e · Cited by 6
Neural Network Modulation of Ayahuasca: A Systematic Review of Human Studies
Santos, G. H. D. M., Rodrigues, L. S., Rocha, J. M., Rossi, G. N., Oña, G., Bouso, J. C., Hallak, J. E. C., & SANTOS, R. G. D. (2023) · Psychoactives · doi:10.3390/psychoactives2010006 · Cited by 7
Self-citationTreatment resistant depression
Vaccarino, S. R., & Kennedy, S. H. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-821033-8.00003-4 · Cited by 7
Prickles and Goo: Human Rights and Spirituality
Sharp, D. N. (2019) · Journal of Human Rights · doi:10.1080/14754835.2020.1856647 · Cited by 9
Psychedelic Medicines in Major Depression: Progress and Future Challenges
Bouso, J. C., Oña, G., SANTOS, R. G. D., & Hallak, J. E. C. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-981-33-6044-0_26 · Cited by 8
Self-citationArgento, E., Capler, R., THOMAS, G. W., Lucas, P., & Tupper, K. W. (2021) · Springer eBooks · doi:10.1007/978-3-030-55688-4_10 · Cited by 6
Imagining a Role for Psychedelics in Dementia Care
George, D. R., & Hanson, R. (2019) · American Journal of Geriatric Psychiatry · doi:10.1016/j.jagp.2019.03.008 · Cited by 6
Vollebregt, R., Storm, A. E. M., Lucassen, P. J., & Somers, M. (2025) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2025.106529 · Cited by 8
Alves, C. L., Ciba, M., Toutain, T. G. L. D. O., Porto, J. A. M., de Sena, E. P., Thielemann, C., & Rodrigues, F. A. (2024) · Journal of Physics Complexity · doi:10.1088/2632-072x/ad1c68 · Cited by 4
Pasquini, L., Simon, A. J., Gallen, C. L., Kettner, H., Roseman, L., Gazzaley, A. H., Carhart-Harris, R. L., & Timmermann, C. (2025) · Imaging Neuroscience · doi:10.1162/imag_a_00541 · Cited by 5
Ayahuasca-inspired DMT/HAR formulation reduces brain differentiation between self and other faces
Suay, D., Aicher, H., Kometer, M., Mueller, M. J., Caflisch, L., Hempe, A., Steinhart, C. P., Elsner, C., Wicki, I. A., Müller, J., et al. (2025) · NeuroImage · doi:10.1016/j.neuroimage.2025.121247 · Cited by 5
Neurobiological Correlates of Psychedelic Experiences and Psychedelic-Associated Adverse Effects
Rieser, N. M., Schmidt, T. T., & Preller, K. H. (2024) · Current topics in behavioral neurosciences · doi:10.1007/7854_2024_507 · Cited by 6
TRADITIONAL MODELS OF FATIGUE AND PHYSICAL PERFORMANCE
de Lima, F. D. R., Brietzke, C., Franco‐Alvarenga, P. E., Asano, R. Y., Viana, B. F., Santos, T. M., & Pires, F. O. (2018) · journal of physical education · doi:10.4025/jphyseduc.v29i1.2915 · Cited by 5
Self-Transcendence Correlates with Brain Function Impairment
Kastrup, B. (2017) · PhilPapers (PhilPapers Foundation) · Cited by 5
Can Biological Quantum Networks Solve NP‐Hard Problems?
Wendin, G. P. (2019) · Advanced Quantum Technologies · doi:10.1002/qute.201800081 · Cited by 5
The Therapeutic Potential of Psilocybin in Alcohol Use Disorder Recovery: A Literature Review
Venugopal, K., & Bedri, N. (2023) · Undergraduate Research in Natural and Clinical Science and Technology (URNCST) Journal · doi:10.26685/urncst.420 · Cited by 5
Balch, J., Grafman, J. H., & McNamara, P. (2023) · Religion Brain & Behavior · doi:10.1080/2153599x.2022.2143398 · Cited by 5
Vitkauskas, M., & Mathuru, A. S. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21186525 · Cited by 5
(2019) · Cambridge University Press eBooks · doi:10.1017/9781316014165 · Cited by 7
McGovern, H. T., Aqil, M., Atasoy, S., & Carhart-Harris, R. L. (2025) · Neuroscience of Consciousness · doi:10.1093/nc/niaf039 · Cited by 6
Navigating through the ebbs and flows of language
Viol, A., Treves, A., & Ciaramelli, E. (2021) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2021.10.009 · Cited by 4
Lawrence, D. W., Battista, A. P. D., & Timmermann, C. (2023) · Journal of Psychoactive Drugs · doi:10.1080/02791072.2023.2230568 · Cited by 4
Psychedelics for Alcohol Use Disorder: A Narrative Review with Candidate Mechanisms of Action
Miller, E. A., Capone, C., Eaton, E. M., Swift, R. M., & Haass‐Koffler, C. L. (2025) · CNS Drugs · doi:10.1007/s40263-025-01199-z · Cited by 6
Ramadam Fasting and Neurologic Disorders
El‐Mitwalli, A. (2019) · Cambridge University Press eBooks · doi:10.1017/9781316014165.013 · Cited by 4
Pennycook, G., Tranel, D., Warner, K., & Asp, E. W. (2019) · Cambridge University Press eBooks · doi:10.1017/9781316014165.012 · Cited by 4
Luppi, A., Hansen, J. Y., Adapa, R., Carhart-Harris, R., Roseman, L., Timmermann, C., Golkowski, D., Ranft, A., Ilg, R., Jordan, D., et al. (2022) · bioRxiv · doi:10.1101/2022.07.12.499688 · Cited by 4
Metadata
- Authors
- Palhano-Fontes, F., Andrade, K. C., Tofoli, L. F., Santos, A. C., Crippa, J. A. S., Hallak, J. E. C., Ribeiro, S., & de Araujo, D. B.
- Affiliations
- Universidade Federal do Rio Grande do Norte (BR)
- Universidade de São Paulo (BR)
- Venue
- PLOS ONE
- Publisher
- Public Library of Science (PLoS)
- Published
- 2015-02-18
- Volume
- 10
- Issue
- 2
- Pages
- e0118143
- ISSN
- 1932-6203 (ISSN-L)
- PMC
- PMC4334486
- OpenAlex
- W2093477837
- Cited by
- 454
- References
- 60
- Citations by year
- 2026: 34 · 2025: 41 · 2024: 45 · 2023: 61 · 2022: 54 · 2021: 49 · 2020: 40 · 2019: 47 · 2018: 31 · 2017: 25 · 2016: 20 · 2015: 6
- FWCI
- 33.90
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- PLoS ONE (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) (publishedVersion, other-oa)
- LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) (publishedVersion, other-oa)
- Americanae (AECID Library) (submittedVersion, other-oa)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Figshare (submittedVersion, cc-by)
- Funders
- Fundação de Amparo à Pesquisa do Estado de São Paulo
- Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
- Conselho Nacional de Desenvolvimento Científico e Tecnológico
- Financiadora de Estudos e Projetos
- Topics
- Social Sciences › Psychology › Clinical Psychology › Psychedelics and Drug Studies
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Life Sciences › Neuroscience › Cognitive Neuroscience › Pain Management and Placebo Effect
- Keywords
- ayahuasca, default mode network, task-positive network, altered states of consciousness, psychedelic effects, posterior cingulate cortex, precuneus, medial prefrontal cortex, functional connectivity, self-reflection, psilocybin, meditation, sleep
- MeSH terms
- Adult, Consciousness Disorders, Female, Gyrus Cinguli, Hallucinogens, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Psilocybin, Prefrontal Cortex, Banisteriopsis, Young Adult, Connectome
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review