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Biology subjects

Luke, D. P.

Publications and source records attributed to Luke, D. P..

2 recordsLinked to original sources

LSD microdosing attenuates the impact of temporal priors in time perception.

Recent theoretical work embedded within the predictive processing framework has proposed that the neurocognitive and therapeutic effects of psychedelics are driven by the modulation of priors (Carhart-Harris & Friston, 2019). We conducted pre-registered re-analyses of previous research (Yanakieva et al., 2019) to examine whether microdoses of lysergic acid diethylamide (LSD) alleviate the temporal reproduction bias introduced by priors, as predicted by this theoretical framework. In a between-groups design, participants were randomly assigned to one of four groups receiving LSD (5, 10, or 20 g) or placebo (0 g) and completed a visual temporal reproduction task spanning subsecond to suprasecond intervals (0.8 to 4 sec). Using mixed-effects modelling, we evaluated the impact of the treatment group, and of the overall history of stimulus intervals (global priors) and the local stimulus history (local priors), weighted by their respective precision weights (inverse of variance), on temporal reproduction. Our principal finding was that the precision-weighted local priors and their precision weights reduced the under-reproduction bias observed under LSD in the original research. Furthermore, controlling for the precision- weighted local prior eliminated the reduced temporal reproduction bias under LSD, indicating that LSD microdosing mitigated the temporal under-reproduction by reducing the relative weighting of priors. These results suggest that LSD microdosing alters human time perception by decreasing the influence of local temporal priors.

neuroscience↗

Primary visual cortex excitability is not atypical in acquired synaesthesia

A wealth of data suggests that psychedelic drugs elicit spontaneous perceptual states that resemble synaesthesia although it is unclear whether these different forms of synaesthesia share overlapping neural mechanisms. Multiple studies have shown that developmental and trained synaesthesia is characterized by selective hyperexcitability in primary visual cortex and it has been proposed that cortical hyperexcitability may contribute to induced and acquired synaesthesia. This study tested the prediction that a case of acquired synaesthesia (LW) would display selectively elevated primary visual cortex excitability, as reflected in lower transcranial magnetic stimulation (TMS) phosphene thresholds, but no difference in motor thresholds, relative to controls. In contrast to this prediction, LWs phosphene threshold was well within the threshold range of controls. These results suggest that acquired synaesthesia is not characterized by atypical visual cortex excitability.

physiology↗