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Research Article

Neural correlates of the psychedelic state as determined by fMRI studies with psilocybin

Robin L. Carhart-Harris, David Erritzoe, Tim Williams, James M. Stone, Laurence J. Reed, Alessandro Colasanti, Robin J. Tyacke, Robert Leech, Andrea L. Malizia, Kevin Murphy, Peter Hobden, John Evans, Amanda Feilding, Richard G. Wise, and David J. Nutt
PNAS February 7, 2012 109 (6) 2138-2143; https://doi.org/10.1073/pnas.1119598109
Robin L. Carhart-Harris
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David Erritzoe
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Tim Williams
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James M. Stone
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Laurence J. Reed
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Alessandro Colasanti
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Robin J. Tyacke
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Robert Leech
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Andrea L. Malizia
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Kevin Murphy
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Peter Hobden
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John Evans
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Amanda Feilding
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Richard G. Wise
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David J. Nutt
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  • For correspondence: d.nutt@imperial.ac.uk
  1. Edited by Leslie Lars Iversen, University of Oxford, Oxford, United Kingdom, and approved December 20, 2011 (received for review December 3, 2011)

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Abstract

Psychedelic drugs have a long history of use in healing ceremonies, but despite renewed interest in their therapeutic potential, we continue to know very little about how they work in the brain. Here we used psilocybin, a classic psychedelic found in magic mushrooms, and a task-free functional MRI (fMRI) protocol designed to capture the transition from normal waking consciousness to the psychedelic state. Arterial spin labeling perfusion and blood-oxygen level-dependent (BOLD) fMRI were used to map cerebral blood flow and changes in venous oxygenation before and after intravenous infusions of placebo and psilocybin. Fifteen healthy volunteers were scanned with arterial spin labeling and a separate 15 with BOLD. As predicted, profound changes in consciousness were observed after psilocybin, but surprisingly, only decreases in cerebral blood flow and BOLD signal were seen, and these were maximal in hub regions, such as the thalamus and anterior and posterior cingulate cortex (ACC and PCC). Decreased activity in the ACC/medial prefrontal cortex (mPFC) was a consistent finding and the magnitude of this decrease predicted the intensity of the subjective effects. Based on these results, a seed-based pharmaco-physiological interaction/functional connectivity analysis was performed using a medial prefrontal seed. Psilocybin caused a significant decrease in the positive coupling between the mPFC and PCC. These results strongly imply that the subjective effects of psychedelic drugs are caused by decreased activity and connectivity in the brain's key connector hubs, enabling a state of unconstrained cognition.

  • default mode network
  • hallucinogens
  • serotonin
  • depression
  • 5-HT2A receptor

Footnotes

  • ↵1To whom correspondence should be addressed. E-mail: d.nutt{at}imperial.ac.uk.
  • Author contributions: R.L.C.-H., J.E., R.G.W., and D.J.N. designed research; R.L.C.-H., D.E., T.W., J.M.S., L.J.R., A.C., R.J.T., R.L., A.L.M., K.M., P.H., J.E., A.F., and R.G.W. performed research; R.L.C.-H., K.M., and R.G.W. analyzed data; and R.L.C.-H., K.M., R.G.W., and D.J.N. wrote the paper.

  • The authors declare no conflict of interest.

  • This article is a PNAS Direct Submission.

  • This article contains supporting information online at www.pnas.org/lookup/suppl/doi:10.1073/pnas.1119598109/-/DCSupplemental.

  • See Commentary on page 1820.

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Neural correlates of the psychedelic state as determined by fMRI studies with psilocybin
Robin L. Carhart-Harris, David Erritzoe, Tim Williams, James M. Stone, Laurence J. Reed, Alessandro Colasanti, Robin J. Tyacke, Robert Leech, Andrea L. Malizia, Kevin Murphy, Peter Hobden, John Evans, Amanda Feilding, Richard G. Wise, David J. Nutt
Proceedings of the National Academy of Sciences Feb 2012, 109 (6) 2138-2143; DOI: 10.1073/pnas.1119598109

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Neural correlates of the psychedelic state as determined by fMRI studies with psilocybin
Robin L. Carhart-Harris, David Erritzoe, Tim Williams, James M. Stone, Laurence J. Reed, Alessandro Colasanti, Robin J. Tyacke, Robert Leech, Andrea L. Malizia, Kevin Murphy, Peter Hobden, John Evans, Amanda Feilding, Richard G. Wise, David J. Nutt
Proceedings of the National Academy of Sciences Feb 2012, 109 (6) 2138-2143; DOI: 10.1073/pnas.1119598109
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