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Psilocybin links binocular rivalry switch rate to attention and subjective arousal levels in humans

Olivia Carter, Felix Hasler, John D. Pettigrew, Guy Wallis, Guang B. Liu, Franz X. Vollenweider

Psychopharmacology September 13, 2007 DOI: 10.1007/s00213-007-0930-9 via OpenAlex

Summary

AI-generated from the abstract

Binocular rivalry, where each eye sees a different image and perception alternates between them, was slowed by psilocybin (215 µg/kg) in ten healthy adults. Pretreatment with ketanserin (50 mg), a 5-HT2A receptor blocker, prevented most of psilocybin's hallucinogenic symptoms but did not reverse the slowing of rivalry switching or the drug's negative-type symptoms such as reduced arousal and vigilance. These findings link slower binocular rivalry switching to subjective levels of arousal and attention, and suggest that psilocybin's effect on rivalry is not mediated by the 5-HT2A receptor.

Study at a glance

Characteristics Experimental study Peer reviewed
Sample size 10
Population Healthy human subjects
Interventions Psilocybin Ketanserin
Dose 215 µg/kg psilocybin, 50 mg ketanserin
Topics LSD Psilocybin Serotonin
Keywords Binocular rivalry Hallucinogen Neuroscience
Citations 150
Key finding Psilocybin significantly reduced the rate of binocular rivalry switching, an effect not blocked by ketanserin, indicating it is unlikely mediated by the 5-HT2A receptor.

Abstract

RationaleBinocular rivalry occurs when different images are simultaneously presented to each eye. During continual viewing of this stimulus, the observer will experience repeated switches between visual awareness of the two images. Previous studies have suggested that a slow rate of perceptual switching may be associated with clinical and drug-induced psychosis.ObjectivesThe objective of the study was to explore the proposed relationship between binocular rivalry switch rate and subjective changes in psychological state associated with 5-HT2A receptor activation.Materials and methodsThis study used psilocybin, the hallucinogen found naturally in Psilocybe mushrooms that had previously been found to induce psychosis-like symptoms via the 5-HT2A receptor. The effects of psilocybin (215 microg/kg) were considered alone and after pretreatment with the selective 5-HT2A antagonist ketanserin (50 mg) in ten healthy human subjects.ResultsPsilocybin significantly reduced the rate of binocular rivalry switching and increased the proportion of transitional/mixed percept experience. Pretreatment with ketanserin blocked the majority of psilocybin's "positive" psychosis-like hallucinogenic symptoms. However, ketanserin had no influence on either the psilocybin-induced slowing of binocular rivalry or the drug's "negative-type symptoms" associated with reduced arousal and vigilance.ConclusionsTogether, these findings link changes in binocular rivalry switching rate to subjective levels of arousal and attention. In addition, it suggests that psilocybin's effect on binocular rivalry is unlikely to be mediated by the 5-HT2A receptor.

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