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Plain numerical DOI: 10.1016/j.euroneuro.2021.10.797
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Plain numerical DOI: 10.1037/scp0000242
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Plain numerical DOI: 10.1016/j.biopsych.2021.02.591
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Plain numerical DOI: 10.1016/j.euroneuro.2021.10.335
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Plain numerical DOI: 10.1136/bmjopen-2021-056091
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Plain numerical DOI: 10.51338/rppsm.2021.v7.i3.241
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Plain numerical DOI: 10.1192/bjb.2023.25
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Plain numerical DOI: 10.2174/2666082218666220513142002
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Plain numerical DOI: 10.7759/cureus.37450
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Plain numerical DOI: 10.7759/cureus.26402
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Plain numerical DOI: 10.1016/bs.apha.2019.03.002
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Plain numerical DOI: 10.1016/s0140-6736(19)31082-7
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Plain numerical DOI: 10.1016/j.drugpo.2019.04.013
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Plain numerical DOI: 10.1101/517847
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Plain numerical DOI: 10.1080/02791072.2019.1593559
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Plain numerical DOI: 10.1037/cns0000169
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Plain numerical DOI: 10.1177/2045125319845774
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Plain numerical DOI: 10.1093/chromsci/bmy104
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Plain numerical DOI: 10.2307/j.ctvc77m52.101
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Plain numerical DOI: 10.1016/j.cca.2019.03.139
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Plain numerical DOI: 10.1038/s41386-019-0324-9
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Plain numerical DOI: 10.1038/s41386-019-0324-9
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Plain numerical DOI: 10.1016/j.euroneuro.2018.11.474
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Plain numerical DOI: 10.1016/j.euroneuro.2018.11.474
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Plain numerical DOI: 10.1016/J.NEUROIMAGE.2019.05.060
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Plain numerical DOI: 10.1016/j.euroneuro.2018.11.224
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Plain numerical DOI: 10.1002/9781444343359.ch11
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Plain numerical DOI: 10.1016/j.pharmthera.2018.11.010
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Plain numerical DOI: 10.1017/neu.2019.15
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“
objective:
psilocybin is a serotonin receptor agonist with a therapeutic potential for treatment-resistant depression and other psychiatric illnesses. we investigated whether the administration of psilocybin had an antidepressant-like effect in a rat model of depression.
methods:
using the flinders sensitive line (fsl) rat model of depression, we assessed the antidepressant-like effect of psilocin and psilocybin, measured as a reduction in immobility time in the forced swim test (fst). we measured locomotor activity in an open field test (oft) to control for stimulant properties of the drugs. we performed a set of experiments to test different doses, treatment paradigms, and timing of the tests in relation to the drug administration.
results:
psilocin and psilocybin showed no effect on immobility, struggling, or swimming behaviour in the fst and no effect on locomotor activity in the oft. fsl rats did show significantly more immobility than their control strain, the flinders resistant line, as expected.
conclusion:
psilocin and psilocybin showed no antidepressant-like effect in the fsl rats, despite a positive effect in humans. this suggests that other animal models of depression and other behavioural tests may be more appropriate for translational studies in the effects of psilocybin.
”
Plain numerical DOI: 10.1016/j.peh.2019.01.001
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Plain numerical DOI: 10.1096/fasebj.2019.33.1_supplement.666.1
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Plain numerical DOI: 10.1096/fasebj.2019.33.1_supplement.666.1
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Plain numerical DOI: 10.1089/jpm.2018.0644
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Plain numerical DOI: 10.1371/journal.pone.0214377
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Plain numerical DOI: 10.1002/chem.201802758
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Plain numerical DOI: 10.1007/s00213-018-5106-2
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objective(s): this pre-registered study aimed to investigate whether microdosing psychedelics is related to differences in personality, mental health, and creativity.
method(s): in this observational study, respondents recruited from online forums self-reported their microdosing behaviors and completed questionnaires concerning dysfunctional attitudes, wisdom, negative emotionality, open-mindedness, and mood. respondents also performed the unusual uses task to assess their creativity.
result(s): current and former microdosers scored lower on measures of dysfunctional attitudes (p < 0.001, r = – 0.92) and negative emotionality (p = 0.009, r = – 0.85) and higher on wisdom (p < 0.001, r = 0.88), openmindedness(p = 0.027, r = 0.67), and creativity (p < 0.001, r = 0.15) when compared to non-microdosing controls.
conclusion(s): these findings provide promising initial evidence that warrants controlled experimental research to directly test safety and clinical efficacy. as microdoses are easier to administer than full-doses, this new paradigm has the exciting potential to shape future psychedelic research.
copyright © 2019, springer-verlag gmbh germany, part of springer nature.”
Plain numerical DOI: 10.1007/s00213-018-5106-2
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objective(s): this pre-registered study aimed to investigate whether microdosing psychedelics is related to differences in personality, mental health, and creativity.
method(s): in this observational study, respondents recruited from online forums self-reported their microdosing behaviors and completed questionnaires concerning dysfunctional attitudes, wisdom, negative emotionality, open-mindedness, and mood. respondents also performed the unusual uses task to assess their creativity.
result(s): current and former microdosers scored lower on measures of dysfunctional attitudes (p < 0.001, r = – 0.92) and negative emotionality (p = 0.009, r = – 0.85) and higher on wisdom (p < 0.001, r = 0.88), openmindedness(p = 0.027, r = 0.67), and creativity (p < 0.001, r = 0.15) when compared to non-microdosing controls.
conclusion(s): these findings provide promising initial evidence that warrants controlled experimental research to directly test safety and clinical efficacy. as microdoses are easier to administer than full-doses, this new paradigm has the exciting potential to shape future psychedelic research.
copyright © 2019, springer-verlag gmbh germany, part of springer nature.”
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copyright © 2019 american psychological association.”
Plain numerical DOI: 10.1016/j.euroneuro.2018.11.477
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Plain numerical DOI: 10.1080/16066359.2018.1455187
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Plain numerical DOI: 10.1177/0333102418804160
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Plain numerical DOI: 10.1016/b978-0-12-815607-0.00033-2
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Plain numerical DOI: 10.1016/j.pnpbp.2019.01.002
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Plain numerical DOI: 10.1016/j.jpainsymman.2018.12.049
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Plain numerical DOI: 10.1016/j.jpainsymman.2018.12.049
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Plain numerical DOI: 10.1007/s00213-018-5106-2
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Plain numerical DOI: 10.1016/j.biopsych.2019.03.460
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Plain numerical DOI: 10.5539/mas.v13n3p13
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Plain numerical DOI: 10.1080/02791072.2019.1581961
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Selected peer-reviewed scientific publications on psilocybin in 2018
Plain numerical DOI: 10.1556/2054.2018.008
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Plain numerical DOI: 10.1089/can.2017.0052
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Plain numerical DOI: 10.1177/1077801217697266
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Plain numerical DOI: 10.1016/bs.pbr.2018.08.004
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Plain numerical DOI: 10.22127/RJP.2018.58486
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Plain numerical DOI: 10.1101/376491
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Plain numerical DOI: 10.1002/chem.201801047
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Plain numerical DOI: 10.1080/16066359.2018.1455187
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Plain numerical DOI: 10.1080/16066359.2018.1455187
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Plain numerical DOI: 10.3389/fphar.2018.00100
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Plain numerical DOI: 10.1101/374199
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Plain numerical DOI: 10.1007/s00213-018-4886-8
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Plain numerical DOI: 10.1021/acschemneuro.8b00101
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Plain numerical DOI: 10.1021/acschemneuro.8b00043
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Plain numerical DOI: 10.1021/acschemneuro.8b00186
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Plain numerical DOI: 10.1093/nc/niy008
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Plain numerical DOI: 10.1101/375105
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Plain numerical DOI: 10.1016/bs.pbr.2018.07.008
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Plain numerical DOI: 10.1177/0269881118793086
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Plain numerical DOI: 10.1007/s00213-018-4981-x
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Plain numerical DOI: 10.1111/acps.12904
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Plain numerical DOI: 10.1080/17512433.2018.1511424
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Plain numerical DOI: 10.1016/j.ymben.2018.05.014
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Plain numerical DOI: 10.1007/7854_2017_478
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Plain numerical DOI: 10.1177/0269881118780713
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Plain numerical DOI: 10.1364/OE.26.025869
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Plain numerical DOI: 10.1002/evl3.42
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Plain numerical DOI: 10.1111/ans.14293
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Plain numerical DOI: 10.1016/j.neuropharm.2017.12.041
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Plain numerical DOI: 10.1177/0269881117748902
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Plain numerical DOI: 10.3389/fphar.2018.00256
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Plain numerical DOI: 10.2217/pmt-2017-0068
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Plain numerical DOI: 10.3389/FPSYG.2018.01721
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Plain numerical DOI: 10.1016/j.jad.2018.01.006
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Plain numerical DOI: 10.1515/dma-2018-0021
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Plain numerical DOI: 10.1016/j.mehy.2018.03.010
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Plain numerical DOI: 10.1177/2050324518767441
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Plain numerical DOI: 10.1002/chem.201802758
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Plain numerical DOI: 10.1038/s41598-018-26656-2
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Plain numerical DOI: 10.3389/fpsyt.2018.00293
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Plain numerical DOI: 10.1007/s00213-017-4807-2
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Plain numerical DOI: 10.1016/j.euroneuro.2018.03.016
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Plain numerical DOI: 10.1007/s00213-017-4771-x
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Plain numerical DOI: 10.1007/s00213-017-4754-y
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Plain numerical DOI: 10.1177/0269881117731279
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Plain numerical DOI: 10.1016/j.scijus.2018.08.005
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Plain numerical DOI: 10.1177/0269881118780612
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Plain numerical DOI: 10.1177/0269881118780612
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Plain numerical DOI: 10.1177/0269881118771782
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Plain numerical DOI: 10.3389/fphar.2018.00733
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Plain numerical DOI: 10.1007/s00213-017-4701-y
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Plain numerical DOI: 10.1080/09540261.2018.1481827
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Plain numerical DOI: 10.1007/978-3-642-55214-4
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Plain numerical DOI: 10.1016/j.neuropharm.2017.12.040
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Plain numerical DOI: 10.3389/fphar.2017.00974
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Plain numerical DOI: 10.1177/0004867418764980
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Plain numerical DOI: 10.1017/S0033291718001356
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Plain numerical DOI: 10.2174/1381612824666180730104707
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Plain numerical DOI: 10.1109/EDUCON.2018.8363404
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Plain numerical DOI: 10.1080/13554794.2018.1468469
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Plain numerical DOI: 10.1007/7854_2016_461
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Plain numerical DOI: 10.1007/7854_2016_461
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Plain numerical DOI: 10.1007/7854_2016_461
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Plain numerical DOI: 10.1016/j.pnpbp.2017.09.012
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Plain numerical DOI: 10.1016/j.biopsych.2018.02.600
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Plain numerical DOI: 10.1089/jpm.2017.0684
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Plain numerical DOI: 10.1007/978-94-024-1194-2_63
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Plain numerical DOI: 10.1007/s00213-017-4713-7
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Plain numerical DOI: 10.1016/j.neuropharm.2018.05.012
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Plain numerical DOI: 10.1556/2054.2018.009
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Plain numerical DOI: 10.3389/fphar.2018.00132
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Plain numerical DOI: 10.1556/2054.2018.003
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Plain numerical DOI: 10.1177/0269881117735685
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Plain numerical DOI: 10.1007/7854_2016_464
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Plain numerical DOI: 10.1007/7854_2016_464
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Plain numerical DOI: 10.1080/09540261.2018.1482261
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Plain numerical DOI: 10.1055/s-0042-108644
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Plain numerical DOI: 10.1016/j.euroneuro.2017.12.114
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“
Introduction
hallucinogen perception persisting disorder (hppd) can be defined as the re-experience of altered visual perceptions after use of psychedelic drugs [1,2]. despite estimated high percentages of recreational use of psychedelic drugs, research data on hppd are scarcely available [1,2]. considering the recent emergence of studies on psychedelic drugs as a treatment option for various psychiatric disorders, proper assessment of potentially harmful side effects, such as hppd, is necessary [3]. this study aims to investigate the association between lifetime use of hppd-associated drugs and the presence and burden of visual hallucinations in a large general population sample.
methods
we used data from a large online survey on hallucinations in the general dutch population, https://zieikspoken.nl, collected between september 26th, 2016 and may 23rd, 2017. all participants (n=10.289) were aged 14 or over. we assessed lifetime use of 11 commonly used recreational drugs in the netherlands, out of which lsd, psilocybin, 2-cb and mdma were considered hppd-associated based on previous reports [1-4]. visual hallucinations were assessed using the questionnaire for psychotic experiences (qpe). presence of visual hallucinations was categorized as follows: never experienced, ever experienced, experienced in past month, experienced in past week. associations between lifetime use of hppd-associated drugs and presence and phenomenology of visual hallucinations were calculated using pearson’s chi-square tests in spss.
results
a total of 2.175 subjects (21.1% of all participants) indicated having used hppd-associated drugs at least once in their lifetime. in subjects who had never experienced visual hallucinations, the percentage of lifetime hppd-associated drug use (18.8%) was significantly lower than in the groups who had experienced visual hallucinations in their lifetime but not recently (23.0%), in the past month (25.2%) or the past week (24.9%). nevertheless, lifetime use of hppd-associated drugs did not differ between the groups of subjects with visual hallucinations (ever/past month/past week). within the group of subjects with visual hallucinations in the past week or month, lifetime hppd-associated drug users did not differ from non-users in terms of experiencing a significant burden from their visual hallucinations (25.2% vs. 24.1%, respectively; or 0.9 (95%-ci 0.7-1.2)) or having visual hallucinations with a signif…”
Plain numerical DOI: 10.1017/ipm.2020.94
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Plain numerical DOI: 10.31887/DCNS.2019.21.2/dnutt
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Plain numerical DOI: 10.1001/jamapsychiatry.2020.3285
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Plain numerical DOI: 10.31887/dcns.2019.21.2
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Plain numerical DOI: 10.1002/pu.30675
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Plain numerical DOI: 10.1016/j.encep.2020.12.002
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Plain numerical DOI: 10.1016/j.jpsychires.2021.05.019
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Plain numerical DOI: 10.1111/acps.13249
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Plain numerical DOI: 10.1556/2054.2019.005
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Plain numerical DOI: 10.1016/j.biopsych.2020.05.015
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Plain numerical DOI: 10.1016/j.encep.2020.12.002
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Plain numerical DOI: 10.1037/hum0000204
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Plain numerical DOI: 10.1136/medethics-2020-106070
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Plain numerical DOI: 10.1016/j.drugalcdep.2021.108648
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Plain numerical DOI: 10.1136/jnnp-2020-bnpa.4
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“
Robin carhart-harris moved to imperial college london in 2008 after obtaining a phd in psychopharmacology from the university of bristol and an ma in psychoanalysis from brunel university. at imperial, he has designed and/or carried out brain imaging studies involving lsd, psilocybin, mdma and dmt, plus a clinical trial of psilocybin for treatment-resistant depression, and an ongoing study comparing psilocybin with escitalopram for major depressive disorder. in 2019, he set-up the centre for psychedelic research at imperial and he also an honorary position with the university of oxford.
the talk takes a multi-level approach to the question of how psychedelics work in the brain. key themes include: the pharmacology of classic serotonergic psychedelics, what this tells us about the function and evolutionary purpose of the serotonin 2a receptor, the acute brain effects of psychedelics as determined by functional brain imaging, the entropic brain hypothesis, current evidence for psychedelic therapy, the ‘Rebus’ hierarchical predictive processing model of the action of psychedelics, and how this maps on to the phenomenology of the acute psychedelic experience and therapeutic outcomes.
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Plain numerical DOI: 10.33735/phimisci.2020.i.39
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Plain numerical DOI: 10.1126/science.372.6544.774
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Plain numerical DOI: 10.3389/fpsyt.2021.687546
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Plain numerical DOI: 10.1080/17512433.2020.1772054
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Plain numerical DOI: 10.1136/jnnp-2020-bnpa.38
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“Aims neurological disorder (fnd), formerly known as conversion disorder, causes a high burden of disability and distress, and is amongst the most commonly encountered conditions in neurology clinics and neuropsychiatry services, yet the therapeutic evidence base is limited. research into psychedelics such as psilocybin and lysergic acid diethylamide (lsd) is currently being undertaken with significant renewed interest, and in recent studies psychedelics have shown promise in treating a range of psychiatric conditions. modification of neural circuits associated with self-representation is thought to underlie some of this effect, and as some contemporary theories of fnd focus on aberrant somatic self-representation, psychedelics may therefore represent an unexplored treatment option for fnd. methods: we systematically reviewed studies involving the use of psychedelics in fnd. nine studies published between 1954 – 1967, with a total of 26 patients, were identified. due to restriction of licencing of psychedelic drugs since this period, no modern studies were identified.
results
lsd was the most commonly used psychedelic, with some studies also using psilocybin and/or mescaline. the number of therapeutic sessions of psychotherapy ± psychedelic substance administration ranged from one to 26, with descriptions of therapeutic methods used widely varying, and in some cases not described in any detail. psychedelics were given either orally or intramuscularly, with doses of lsd ranging from 25 to 2,000 micrograms (mcg), and doses of psilocybin ranging from 3 to 15 milligrams (mg). of those treated, 69% (n=18) were found to have made at least some recovery, with 23% (n=6) having completely recovered after psychedelic therapy. adverse events were typically mild and transient.
conclusions
studies were generally of low quality, often lacking control groups and valid outcome measures. despite this, the degree of improvement is considerable, even if the presumptive bias in favour of the treatment in the studies is taken into consideration. furthermore, good therapeutic outcomes and lack of adverse events in modern open-label trials utilising psychedelic therapy for neuropsychiatric disorders is encouraging. advances in the understanding of the neurobiology of fnd, as well as further modern clinical research into the therapeutic utility of psychedelics, may help to determine whether psychedelics offer a feasible, safe and effective treatmen…”
Plain numerical DOI: 10.18261/ISSN.1504-291X-2020-04-03
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Plain numerical DOI: 10.1007/978-3-642-36172-2_43
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Plain numerical DOI: 10.1016/j.jpsychires.2021.03.002
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Plain numerical DOI: 10.1139/cjb-2020-0006
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Plain numerical DOI: 10.1016/j.euroneuro.2020.09.220
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Plain numerical DOI: 10.1037/pha0000490
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Plain numerical DOI: 10.4324/9780429061196
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