Psychedelics
By David E. Nichols. Pharmacological Reviews, 2016
1,421 citations recorded by the source corpus.
Subfields: Clinical Psychology, Molecular Biology, Organic Chemistry
View Paper: https://www.semanticscholar.org/paper/d103f7fdab5b4716b1ac3bc4a1eb30451e76f0a1
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Clinical Psychology
- Robin L. Carhart-Harris
- David J. Nutt
- Karl J. Friston
- Leor Roseman
- Roland R. Griffiths
- Matthew W. Johnson
- R. Watts
- Camilla M. Day
In Molecular Biology
- Robin L. Carhart-Harris
- Karl J. Friston
- Roland R. Griffiths
- David J. Nutt
- Matthew W. Johnson
- Mary P Cosimano
- Chris Letheby
- Melody Andrews
In Organic Chemistry
- Robin L. Carhart-Harris
- David J. Nutt
- Karl J. Friston
- Leor Roseman
- Roland R. Griffiths
- Matthew W. Johnson
- R. Watts
- Chris Letheby
Citations in the corpus
- REBUS and the Anarchic Brain: Toward a Unified Model of the Brain Action of Psychedelics (2019, background): “Some classic psychedelics, such as LSD, have a rich pharmacology (Nichols, 2004, 2016); however, there is compelling evidence that activation of a specific serotonin receptor subtype, the 5-HT2AR, is necessary for these compounds ’ subsequent psychedelic effects.”
- Rapid and sustained symptom reduction following psilocybin treatment for anxiety and depression in patients with life-threatening cancer: a randomized controlled trial (2016, background): “In two recently published open-label trials, one using a single dose of ayahuasca (Osorio et al., 2015) and the other using two doses of oral psilocybin (Carhart-Harris et al., 2016), acute and enduring anti-depressant effects were reported.”
- 5-HT2C Receptor Structures Reveal the Structural Basis of GPCR Polypharmacology (2018, neutral): “Creating selective 5-HT2C agonists is extremely challenging, however, as off-target agonist activity at the closely related 5-HT2A and 5-HT2B receptors leads to lysergic acid diethylamide (LSD)-like hallucinations (Nichols, 2016) and cardiac valvulopathy (Roth, 2007), respectively.”
- Patients’ Accounts of Increased “Connectedness” and “Acceptance” After Psilocybin for Treatment-Resistant Depression (2017, background): “Recent clinical trials have found promising safety, tolerability, and efficacy (Nichols, 2016).”
- Quality of Acute Psychedelic Experience Predicts Therapeutic Efficacy of Psilocybin for Treatment-Resistant Depression (2018, background): “Like SSRIs, classic psychedelic drugs also work on the serotonin system; however, unlike the SSRIs, they are direct agonists at the 5-HT2A receptor (Nichols, 2016).”
- Being for no-one (2020, background): “Like other “classic” psychedelics such as LSD and psilocybin, they are believed to alter consciousness primarily via 5-HT2A receptor agonism (Nichols, 2016).”
- Psychedelics Promote Structural and Functional Neural Plasticity (2018, background): “Moreover, several psychedelics elevate glutamate levels in the cortex (Nichols, 2004, 2016) and increase gene expression in vivo of the neuro-trophin BDNF as well as immediate-early genes associated with plasticity (Martin et al., 2014; Nichols and Sanders-Bush, 2002; Vaidya et al., 1997).”
- Psilocybin produces substantial and sustained decreases in depression and anxiety in patients with life-threatening cancer: A randomized double-blind trial (2016, background): “The classic hallucinogens, which include psilocybin (psilocin) and (+)-lysergic acid diethylamide (LSD), are a structurally diverse group of compounds that are 5-HT2A receptor agonists and produce a unique profile of changes in thoughts, perceptions, and emotions (Halberstadt, 2015; Nichols, 2016).”