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1.
Br J Psychiatry ; 200(3): 238-44, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22282432

ABSTRACT

BACKGROUND: Psilocybin is a classic psychedelic drug that has a history of use in psychotherapy. One of the rationales for its use was that it aids emotional insight by lowering psychological defences. AIMS: To test the hypothesis that psilocybin facilitates access to personal memories and emotions by comparing subjective and neural responses to positive autobiographical memories under psilocybin and placebo. METHOD: Ten healthy participants received two functional magnetic resonance imaging scans (2 mg intravenous psilocybin v. intravenous saline), separated by approximately 7 days, during which they viewed two different sets of 15 positive autobiographical memory cues. Participants viewed each cue for 6 s and then closed their eyes for 16 s and imagined re-experiencing the event. Activations during this recollection period were compared with an equivalent period of eyes-closed rest. We split the recollection period into an early phase (first 8 s) and a late phase (last 8 s) for analysis. RESULTS: Robust activations to the memories were seen in limbic and striatal regions in the early phase and the medial prefrontal cortex in the late phase in both conditions (P<0.001, whole brain cluster correction), but there were additional visual and other sensory cortical activations in the late phase under psilocybin that were absent under placebo. Ratings of memory vividness and visual imagery were significantly higher after psilocybin (P<0.05) and there was a significant positive correlation between vividness and subjective well-being at follow-up (P<0.01). CONCLUSIONS: Evidence that psilocybin enhances autobiographical recollection implies that it may be useful in psychotherapy either as a tool to facilitate the recall of salient memories or to reverse negative cognitive biases.


Subject(s)
Emotions/drug effects , Hallucinogens/therapeutic use , Magnetic Resonance Imaging/methods , Memory/drug effects , Psilocybin/therapeutic use , Adult , Brain/physiology , Brain Mapping , Combined Modality Therapy , Cross-Over Studies , Female , Hallucinogens/pharmacology , Humans , Male , Memory/physiology , Memory, Episodic , Placebos , Psilocybin/pharmacology , Psychotherapy
2.
Neuroimage ; 30(4): 1112-20, 2006 May 01.
Article in English | MEDLINE | ID: mdl-16473021

ABSTRACT

The medial geniculate body (MGB) of the thalamus is a key component of the auditory system. It is involved in relaying and transforming auditory information to the cortex and in top-down modulation of processing in the midbrain, brainstem, and ear. Functional imaging investigations of this region in humans, however, have been limited by the difficulty of distinguishing MGB from other thalamic nuclei. Here, we introduce two methods for reliably delineating MGB anatomically in individuals based on conventional and diffusion MRI data. The first uses high-resolution proton density weighted scanning optimized for subcortical grey-white contrast. The second uses diffusion-weighted imaging and probabilistic tractography to automatically segment the medial and lateral geniculate nuclei from surrounding structures based on their distinctive patterns of connectivity to the rest of the brain. Both methods produce highly replicable results that are consistent with published atlases. Importantly, both methods rely on commonly available imaging sequences and standard hardware, a significant advantage over previously described approaches. In addition to providing useful approaches for identifying the MGB and LGN in vivo, our study offers further validation of diffusion tractography for the parcellation of grey matter regions on the basis of their connectivity patterns.


Subject(s)
Auditory Pathways/anatomy & histology , Diffusion Magnetic Resonance Imaging , Geniculate Bodies/anatomy & histology , Image Processing, Computer-Assisted , Magnetic Resonance Imaging , Thalamic Nuclei/anatomy & histology , Adult , Auditory Cortex/anatomy & histology , Auditory Perception/physiology , Brain Mapping , Brain Stem/anatomy & histology , Dominance, Cerebral/physiology , Female , Humans , Male , Reference Values
3.
J Neurophysiol ; 90(1): 313-9, 2003 Jul.
Article in English | MEDLINE | ID: mdl-12843312

ABSTRACT

Umami taste stimuli, of which an exemplar is monosodium glutamate (MSG) and which capture what is described as the taste of protein, were shown using functional MRI (fMRI) to activate similar cortical regions of the human taste system to those activated by a prototypical taste stimulus, glucose. These taste regions included the insular/opercular cortex and the caudolateral orbitofrontal cortex. A part of the rostral anterior cingulate cortex (ACC) was also activated. When the nucleotide 0.005 M inosine 5'-monophosphate (IMP) was added to MSG (0.05 M), the blood oxygenation-level dependent (BOLD) signal in an anterior part of the orbitofrontal cortex showed supralinear additivity; this may reflect the subjective enhancement of umami taste that has been described when IMP is added to MSG. These results extend to humans previous studies in macaques showing that single neurons in these taste cortical areas can be tuned to umami stimuli.


Subject(s)
Cerebral Cortex/physiology , Inosine Monophosphate , Sodium Glutamate , Taste/physiology , Brain/physiology , Brain Mapping , Female , Glucose/administration & dosage , Humans , Inosine Monophosphate/administration & dosage , Magnetic Resonance Imaging , Male , Sodium Glutamate/administration & dosage , Time Factors
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