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Nadia R P W Hutten

Researcher at Maastricht University

Publications -  25
Citations -  531

Nadia R P W Hutten is an academic researcher from Maastricht University. The author has contributed to research in topics: Cannabis & Placebo. The author has an hindex of 10, co-authored 23 publications receiving 236 citations.

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Me, myself, bye: regional alterations in glutamate and the experience of ego dissolution with psilocybin

TL;DR: It is demonstrated that psilocybin induced region-dependent alterations in glutamate, which predicted distortions in the subjective experience of one’s self (ego dissolution), which may provide a neurochemical basis for therapeutic effects as witnessed in ongoing clinical trials.
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Motives and Side-Effects of Microdosing With Psychedelics Among Users.

TL;DR: The majority of users microdosed to enhance performance, but the main reason to have stopped microdosing was that it was not effective, and future experimental placebo-controlled studies are needed to test whether performance enhancement can be quantified and to assess potential negative effects after longer term microdoses.
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Low Doses of LSD Acutely Increase BDNF Blood Plasma Levels in Healthy Volunteers.

TL;DR: The finding that LSD acutely increases BDNF levels warrants studies in patient populations, based on preclinical evidence for psychedelic-induced neuroplasticity in humans.
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Mood and cognition after administration of low LSD doses in healthy volunteers: A placebo controlled dose-effect finding study

TL;DR: Overall, the present study demonstrated selective, beneficial effects of low doses of LSD on mood and cognition in the majority of observations, and the minimal LSD dose at which subjective and performance effects are notable is 5 mcg and the most apparent effects were visible after 20 mcg.
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Cannabis induced increase in striatal glutamate associated with loss of functional corticostriatal connectivity

TL;DR: This double-blind, placebo-controlled study suggests that THC elicits subjective and cognitive alterations via increased striatal dopaminergic activity and loss of corticostriatal connectivity, which is associated with an increase in striatal glutamate.