Alonso et al. (2015) reported that psychedelics reduce Default Mode Network (DMN) integrity and cause disintegration in normal system functions by reducing connectivity between the frontal cortex and lower brain areas.
Psychedelic experiences do not typically manifest operators that depend on higher-level cognitive integration provided by the prefrontal cortex (PFC) or the self and autobiographical qualities maintained by the Default Mode Network (DMN).
Speech production is compromised under LSD because of the lack of connections with the neocortical components involving the frontal lobe (Broca's area), while the language capacity for understanding meaning persists because of its lower anatomical basis near the Default Mode Network (DMN) component, the inferior parietal lobule in the superior temporal gyrus (Wernicke's area).
Uddin et al. published 'Functional connectivity of default mode network components: correlation, anticorrelation, and causality' in Human Brain Mapping in 2009 (Hum. Brain Mapp. 30, 625–637).
Barrett and Griffiths (2017) identified parallels in the neural bases of psychedelic and meditative effects on the Default Mode Network (DMN), specifically hypothesizing that visionary experiences result from decreased activity and functional connectivity in the medial nodes of the DMN (PCC and MPFC), which mediate self-referential processing.
Raichle (2015) concluded that the cortico-cortical axonal pathways involve a structural core comprised of the posterior medial cortex and parietal cerebral cortex, as well as the temporal and frontal modules that link all major structural hubs of the brain through the posterior areas of the Default Mode Network.
The hypothesis that innate operators explain features of psychedelic experiences is supported by evidence of innate modular functions in entoptic images (Siegel, 1977), the modular structure of the human brain (Gardner, 1983, 2000), cognitive science of religion explanations for supernatural experiences (Boyer, 2001, 2017; Clements, 2017), and the relationship of the MNS (Mirror Neuron System) to the DMN (Default Mode Network) and mimesis (Garrels, 2006, 2011).
Visionary experiences across diverse modes of altering consciousness share a common mechanism released by the interruption of the prefrontal cortex (PFC) and the default mode network (DMN).
The Default Mode Network is functionally and anatomically connected with the thalamus and precuneus, a connectivity that is crucial to consciousness, according to Cunningham et al. (2017).
Dos Santos et al. (2016) noted that variations in study results regarding psychedelic effects on the Default Mode Network may be attributed to differences in the phase of the experience studied, drug dosage, measurement time-scales, and the route of administration (oral vs. intravenous).
The common mechanisms underlying diverse alterations of consciousness involve the disruption of normal functions in the prefrontal cortex and the default mode network (DMN).
The activation or disinhibition of areas within the dorsal medial subsystem of the Default Mode Network (DMN), which manages social information, is implicated in the high importance of a social 'other' in some mystical experiences.
Psychedelic use results in reduced functional connectivity among areas of the Default Mode Network.
Psychedelics and other processes that alter consciousness share common mechanisms involving the disabling of the prefrontal cortex and default mode networks.
The neural correlates of out-of-body experiences involve a disruption of a specific Default Mode Network (DMN) area, the temporo-parietal junction (TPJ), which integrates bodily and sensory modalities.
The anterior cingulate cortex (ACC) provides a locus for the interaction between the default mode network (DMN) and the mirror neuron system (MNS), as reported by Uddin et al. (2007).
Disruption of the Default Mode Network (DMN) may account for the frequently reported sense of ineffability, defined as the inability to express the psychedelic experience in words.
Egoless experiences, measured as 'oceanic boundlessness,' are associated with alterations in the frontolimbic-parieto-striatal network and are positively correlated with cerebral glucose metabolism in Default Mode Network regions (anterior cingulate cortex, hippocampus, inferior parietal cortex) and prefrontal cortex areas (frontomedial superior, frontolateral, and left inferolateral).
Epileptic seizures, including complex partial, generalized tonic-clonic, and absence seizures, impair primary nodes of the Default Mode Network (DMN), specifically the precuneus/PCC, medial frontal cortex, lateral parietal cortex, and the anterior cingulate cortex (ACC), resulting in long-lasting decreases in DMN activity.
Reduced activity and connectivity within the Default Mode Network (DMN) are observed in both psychedelic use and various non-pharmacological methods for altering consciousness.
Decreased integrity of the Default Mode Network is reflected by decreased functional connectivity between the parahippocampus and retrosplenial cortex, the magnitude of which is strongly correlated with self-report ratings of spiritual experience and ego-dissolution, according to Kometer et al. (2013), Lebedev et al. (2015), Carhart-Harris et al. (2016), and Tagliazucchi et al. (2016).
The reduction in oscillatory activity and power in the Default Mode Network caused by psilocybin results from decreased functional coupling between the frontal cortex and the medial temporal lobe components of the Default Mode Network, as well as between the medial prefrontal cortex and the posterior cingulate cortex.
The 2016 review by dos Santos et al. reported a decrease in functional connectivity between key hubs of the Default Mode Network (DMN), specifically noting a reduction in connectivity between the posterior cingulate cortex (PCC) and the anterior cingulate cortex (ACC).
The paper 'Internal and external attention and the default mode network' by H. Scheibnera, C. Bogler, T. Gleich, C.J.-D. Haynes, and F. Bermpohla, published in NeuroImage in 2017, discusses the default mode network's role in attention.
Brewer et al. (2011) found that meditation experience is associated with differences in default mode network activity and connectivity, as published in the Proceedings of the National Academy of Sciences of the United States of America.
The mirror neuron system (MNS) and the medial prefrontal cortex (mPFC) node of the default mode network (DMN) interact significantly during mentalizing and embodied simulation processes, according to Molnar-Szakacs and Uddin (2013).
Positive emotional experiences and profound quiescence of meditative practices result from a deafferentation of limbic stimulation from the peripheral parasympathetic system, combined with reverberating parietal lobule connections with Prefrontal Cortex (PFC) circuits that result in stimulation of both divisions of the Autonomic Nervous System and enhanced connections of the sensory association areas with the inferior parietal lobe, a key Default Mode Network (DMN) area.
High-hypnotizability subjects exhibit greater decreases in Default Mode Network (DMN) activity, particularly in the dorsal anterior cingulate cortex (ACC), and reduced connectivity between the posterior cingulate cortex (PCC) and the Executive Control Network, according to a 2017 study by Jiang et al.
Psychedelics cause reduced activity in the Default Mode Network's hub structures, which leads to a reduction in oscillatory activity and network integrity, as documented by Carhart-Harris et al. (2012, 2016), Muthukumaraswamy et al. (2013), and Palhano-Fontes et al. (2015).
Palhano-Fontes et al. (2015) found that the psychedelic state induced by ayahuasca modulates the activity and connectivity of the default mode network in the human brain.
Washington and VanMeter published 'Anterior-posterior connectivity within the default mode network increases during maturation' in the International Journal of Medical and Biological Frontiers in 2015 (Int. J. Med. Biol. Front. 21, 207–218).
Panda et al. (2016) found that temporal dynamics of the default mode network characterize meditation-induced alterations in consciousness.
The "meaning" network involved in understanding verbal and visual events overlaps with major areas of the Default Mode Network (DMN) and involves brain areas recognized for their role in semantic memory, embodied simulation, and visuo-spatial scene representation, according to Jouena et al. (2015).
A 2016 study by Panda et al. using EEG and fMRI compared 20 Raja Yoga expert meditators to a control group and found that meditators had significant reductions in activity and connectivity of the posterior cingulate hub of the Default Mode Network.
The major subdivisions of the Default Mode Network include the ventral medial and dorsal medial regions of the prefrontal cortex, the posterior cingulate cortex (PCC) with the precuneus, and the lateral parietal cortex.
The Default Mode Network (DMN) is based in the medial and lateral cortices of the parietal and temporal lobes, as well as the medial prefrontal cortex (mPFC), according to Raichle (2015).
Psychedelics increase functional connectivity between normally disconnected brain networks, which contrasts with their acute effect of reducing functional connectivity within the Default Mode Network.
Raichle (2015) provided an overview of the brain's default mode network in the 'Annual Review of Neuroscience'.
The psychedelic-induced disruption of Default Mode Network (DMN) self-related functions likely causes the changes in the experience of self and the relationship to a spiritual 'other' typical of personalized theistic mystical experiences.
The disruption of top-down control mediated by the prefrontal cortex (PFC) and the compromise of self-referencing processes in the default mode network (DMN) leads to the emergence of processes from lower-level brain systems, which manifest as innate intelligences, modules, and operators.
The major types of meditation techniques, specifically Concentration, Loving-Kindness, and Choiceless Awareness, produce a relative deactivation in the main nodes of the Default Mode Network (DMN) in experienced meditators, according to a 2011 study by Brewera et al.
Psychedelic-induced mystical effects are partly the result of inhibiting the normal functions of the Default Mode Network (DMN).
Palhano-Fontes et al. (2015) found that ayahuasca consumption causes a significant decrease in activity throughout most parts of the Default Mode Network, particularly in the posterior cingulate cortex, precuneus, and medial prefrontal cortex, while also reducing functional connectivity within the posterior cingulate cortex/precuneus.
The interruption of the Default Mode Network (specifically the posterior cingulate cortex) by meditation, hypnosis, and epilepsy necessitates a general explanation for psychedelic effects within the broader context of altered consciousness.
Washington and VanMeter (2015) characterized the connectivity between the dorsal and ventral regions of the medial prefrontal cortex (mPFC) and the dorsal and ventral areas of the anterior cingulate cortex (ACC) as the most anterior area of functional connectivity within the default mode network (DMN).
The Default Mode Network primarily involves connections among the thalamus, posterior cingulate cortex (PCC), medial prefrontal cortex (mPFC), and areas of the limbic system (parahippocampal cortex and the hippocampus) that function as a network for information routing and integration, as described by Buckner et al. (2008).
Psychedelics, meditation, hypnosis, and epilepsy all cause an interruption of ordinary brain control processes by compromising the integrity of the Default Mode Network (DMN) and its connectivity with other brain areas, particularly the prefrontal cortex (PFC).
The Default Mode Network (DMN) connection with the Mirror Neuron System (MNS) is stimulated by increased activation of right fronto-parietal regions, which overlap with MNS areas involved in mapping the actions of others via simulation within one's own motor system, according to Molnar-Szakacs and Uddin (2013).
Muthukumaraswamy et al. (2013) found that psilocybin caused a reduction in oscillatory activity and power in posterior and frontal association cortices and the Default Mode Network.
Destabilization of habitual cognitive mechanisms, specifically the Default Mode Network, reduces top-down brain dynamics and facilitates bottom-up information transfer.
Hypnosis reduces activity in the anterior areas of the Default Mode Network (DMN), with the depth of attentional absorption induced by hypnosis correlating with the degree of DMN activity reduction, according to studies by McGeown et al. (2009) and Deeley et al. (2012).