RETRACTED ARTICLE: A mechanistic model of the neural entropy increase elicited by psychedelic drugs

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作者
Rubén Herzog
Pedro A. M. Mediano
Fernando E. Rosas
Robin Carhart-Harris
Yonatan Sanz Perl
Enzo Tagliazucchi
Rodrigo Cofre
机构
[1] Universidad de Valparaíso,Centro Interdisciplinario de Neurociencia de Valparaíso
[2] University of Cambridge,Department of Psychology
[3] Imperial College London,Department of Brain Science, Centre for Psychedelic Research
[4] Imperial College London,Data Science Institute
[5] Imperial College London,Centre for Complexity Science
[6] University of Buenos Aires,Buenos Aires Physics Institute and Physics Department
[7] National Scientific and Technical Research Council,CIMFAV
[8] Universidad de San Andres,Ingemat, Facultad de Ingeniería
[9] Universidad de Valparaíso,undefined
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摘要
Psychedelic drugs, including lysergic acid diethylamide and other agonists of the serotonin 2A receptor (5HT2A-R), induce drastic changes in subjective experience, and provide a unique opportunity to study the neurobiological basis of consciousness. One of the most notable neurophysiological signatures of psychedelics, increased entropy in spontaneous neural activity, is thought to be of relevance to the psychedelic experience, mediating both acute alterations in consciousness and long-term effects. However, no clear mechanistic explanation for this entropy increase has been put forward so far. We sought to do this here by building upon a recent whole-brain model of serotonergic neuromodulation, to study the entropic effects of 5HT2A-R activation. Our results reproduce the overall entropy increase observed in previous experiments in vivo, providing the first model-based explanation for this phenomenon. We also found that entropy changes were not uniform across the brain: entropy increased in some regions and decreased in others, suggesting a topographical reconfiguration mediated by 5HT2A-R activation. Interestingly, at the whole-brain level, this reconfiguration was not well explained by 5HT2A-R density, but related closely to the topological properties of the brain’s anatomical connectivity. These results help us understand the mechanisms underlying the psychedelic state and, more generally, the pharmacological modulation of whole-brain activity.
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