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ACS Chemical Neuroscience

ISSN 1948-7193

100 papers in the library · 2,538 citations · publishing 2010-2026

Papers

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Role of Serotonin Transporter and Receptor Gene Variations in the Acute Effects of MDMA in Healthy Subjects

ACS Chemical Neuroscience December 27, 2018 Patrick Vizeli, Henriette E. Meyer zu Schwabedissen, Matthias E. Liechti 13 citations

Methylenedioxymethamphetamine (MDMA; ecstasy) is used recreationally and has been investigated as an adjunct to psychotherapy. Most acute effects of MDMA can be attributed to activation of the serotonin (5-hydroxytryptamine [5-HT]) system. Genetic variants, such as single-nucleotide polymorphisms (SNPs) and polymorphic regions in 5-HT system genes, may contribute to interindividual differences...

DARK Classics in Chemical Neuroscience: Phencyclidine (PCP).

ACS Chemical Neuroscience October 17, 2018 Jeanette L Bertron, Mabel Seto, Craig W Lindsley

Phencyclidine (PCP, "angel dust", an arylcyclohexylamine) was the first non-natural, man-made illicit drug of abuse, and was coined 'the most dangerous drug in America" in the late 1970s (amidst sensational horror stories of the drug's effects); however, few other illicit drugs have had such a significant and broad impact on society-both good and bad. Originally developed as a new class of...

DARK Classics in Chemical Neuroscience: Aminorex Analogues

ACS Chemical Neuroscience September 30, 2018 Julian Maier, Felix P. Mayer, Simon D. Brandt et al. 15 citations

Aminorex (5-phenyl-4,5-dihydro-1,3-oxazol-2-amine) and 4-methylaminorex (4-methyl-5-phenyl-4,5-dihydro-1,3-oxazol-2-amine) are psychostimulants that have long been listed in Schedules IV and I of the UN Convention on Psychotropic Substances of 1971. However, a range of psychoactive analogues exist that are not internationally controlled and therefore often classified as new psychoactive...

Understanding Central Nervous System Effects of Deliriant Hallucinogenic Drugs through Experimental Animal Models

ACS Chemical Neuroscience September 25, 2018 Andrey D. Volgin, Oleg A. Yakovlev, Konstantin A. Demin et al. 38 citations

Hallucinogenic drugs potently alter human behavior and have a millennia-long history of use for medicinal and religious purposes. Interest is rapidly growing in their potential as CNS modulators and therapeutic agents for brain conditions. Antimuscarinic cholinergic drugs, such as atropine and scopolamine, induce characteristic hyperactivity and dream-like hallucinations and form a separate...

DOI: 10.1021/acschemneuro.8b00433 (opens in new tab) Hallucinogen Cholinergic Pharmacology Parasympatholytic +4

DARK Classics in Chemical Neuroscience: Ibogaine

ACS Chemical Neuroscience September 14, 2018 Michael Wasko, Paula A. Witt‐enderby, Christopher K. Surratt 63 citations

The West African iboga plant has been used for centuries by the Bwiti and Mbiri tribes to induce hallucinations during religious ceremonies. Ibogaine, the principal alkaloid responsible for iboga's psychedelic properties, was isolated and sold as an antidepressant in France for decades before its adverse effects precipitated its removal from the market. An ibogaine resurgence in the 1960s was...

DOI: 10.1021/acschemneuro.8b00294 (opens in new tab) Hallucinogen Nicotine Synthetic cannabinoids Nicotinic acetylcholine receptor +2

Dark Classics in Chemical Neuroscience:N,N-Dimethyltryptamine (DMT)

ACS Chemical Neuroscience July 23, 2018 Lindsay P. Cameron, David E. Olson 114 citations

Though relatively obscure, N, N-dimethyltryptamine (DMT) is an important molecule in psychopharmacology as it is the archetype for all indole-containing serotonergic psychedelics. Its structure can be found embedded within those of better-known molecules such as lysergic acid diethylamide (LSD) and psilocybin. Unlike the latter two compounds, DMT is ubiquitous, being produced by a wide variety...

Dark Classics in Chemical Neuroscience: 3,4-Methylenedioxymethamphetamine

ACS Chemical Neuroscience July 12, 2018 Lee E. Dunlap, Anne M. Andrews, David E. Olson 105 citations

Better known as "ecstasy", 3,4-methylenedioxymethamphetamine (MDMA) is a small molecule that has played a prominent role in defining the ethos of today's teenagers and young adults, much like lysergic acid diethylamide (LSD) did in the 1960s. Though MDMA possesses structural similarities to compounds like amphetamine and mescaline, it produces subjective effects that are unlike any of the...

DARK Classics in Chemical Neuroscience: Psilocybin

ACS Chemical Neuroscience June 29, 2018 Haden A. Geiger, Madeline G. Wurst, R. Nathan Daniels 139 citations

Psilocybin is found in a family of mushrooms commonly known as "magic mushrooms" that have been used throughout history to induce hallucinations. In the late 1950s Albert Hofmann, of Sandoz Laboratories, identified and synthesized the psychoactive compounds psilocybin and psilocin which are found in psilocybe mushrooms. Psilocybin was marketed by Sandoz as Indocybin for basic...

DOI: 10.1021/acschemneuro.8b00186 (opens in new tab) Psilocybin Hallucinogen Alcohol addiction Pharmacology

Psychedelics and Personality

ACS Chemical Neuroscience June 4, 2018 Marc Aixalà, Rafael G. Dos Santos, Jaime E. C. Hallak et al. 14 citations

In the past decade, an increasing number of clinical trials are reporting evidence that psychedelics or serotonergic hallucinogens (such as lysergic acid diethylamide, psilocybin, and ayahuasca/dimethyltryptamine) could be effective in the treatment of mood, anxiety, and substance use disorders. The mechanisms responsible for these effects are not fully understood but seem to involve changes in...

Dark Classics in Chemical Neuroscience: Mescaline

ACS Chemical Neuroscience May 30, 2018 Bruce K. Cassels, Patricio Sáez-briones 84 citations

Archeological studies in the United States, Mexico, and Peru suggest that mescaline, as a cactus constituent, has been used for more than 6000 years. Although it is a widespread cactus alkaloid, it is present in high concentrations in few species, notably the North American peyote ( Lophophora williamsii) and the South American wachuma ( Trichocereus pachanoi, T. peruvianus, and T. bridgesii)....

Classics in Neuroimaging: The Serotonergic 2A Receptor System—from Discovery to Modern Molecular Imaging

ACS Chemical Neuroscience May 15, 2018 Elina Tampio L’Estrade, Hanne Demant Hansen, Maria Erlandsson et al. 14 citations

High Resolution Image Download MS PowerPoint Slide Already in 1953, Woolley and Shaw speculated that serotonin could be involved in a range of central nervous system (CNS) disorders. Lysergic acid diethylamide (LSD) displayed an important role in this respect. It was used not only to antagonize biological effects of serotonin and to study the system itself, but also to identify serotonergic...

DARK Classics in Chemical Neuroscience: Cathinone-Derived Psychostimulants.

ACS Chemical Neuroscience May 11, 2018 Steven J Simmons, Jonna M Leyrer-Jackson, Chicora F Oliver et al.

Cathinone is a plant alkaloid found in khat leaves of perennial shrubs grown in East Africa. Similar to cocaine, cathinone elicits psychostimulant effects which are in part attributed to its amphetamine-like structure. Around 2010, home laboratories began altering the parent structure of cathinone to synthesize derivatives with mechanisms of action, potencies, and pharmacokinetics permitting...

Effects of N,N-Dimethyltryptamine on Rat Behaviors Relevant to Anxiety and Depression

ACS Chemical Neuroscience April 17, 2018 Lindsay P. Cameron, Charlie J. Benson, Lee E. Dunlap et al. 168 citations

Depression and anxiety disorders are debilitating diseases resulting in substantial economic costs to society. Traditional antidepressants often take weeks to months to positively affect mood and are ineffective for about 30% of the population. Alternatives, such as ketamine, a dissociative anesthetic capable of producing hallucinations, and the psychoactive tisane ayahuasca, have shown great...

Dark Classics in Chemical Neuroscience: Lysergic Acid Diethylamide (LSD)

ACS Chemical Neuroscience February 20, 2018 David E. Nichols 87 citations

Lysergic acid diethylamide (LSD) is one of the most potent psychoactive agents known, producing dramatic alterations of consciousness after submilligram (≥20 μg) oral doses. Following the accidental discovery of its potent psychoactive effects in 1943, it was supplied by Sandoz Laboratories as an experimental drug that might be useful as an adjunct for psychotherapy, or to give psychiatrists...

The DARK Side of Total Synthesis: Strategies and Tactics in Psychoactive Drug Production.

ACS Chemical Neuroscience February 1, 2018 Schuyler A Chambers, Jenna M DeSousa, Eric D Huseman et al.

Humankind has used and abused psychoactive drugs for millennia. Formally, a psychoactive drug is any agent that alters cognition and mood. The term "psychotropic drug" is neutral and describes the entire class of substrates, licit and illicit, of interest to governmental drug policy. While these drugs are prescribed for issues ranging from pain management to anxiety, they are also used...

DOI: 10.1021/acschemneuro.7b00528 (opens in new tab) Full text (opens in new tab) Humans Substance-related disorders Amphetamines N-methyl-3,4-methylenedioxyamphetamine +20

Classics in Chemical Neuroscience: Ketamine.

ACS Chemical Neuroscience June 21, 2017 Marshall Tyler, Harmony B Yourish, Dawn F. Ionescu et al.

Ketamine, a molecule of many faces, has contributed immeasurably to numerous realms of clinical practice and scientific inquiry. From anesthesia and analgesia to depression and schizophrenia, it continues to shed light on the molecular underpinnings of pain, consciousness, and the pathophysiology of neuropsychiatric disorders. In particular, research on ketamine's mechanism of action is...

N-Methyl-d-aspartate Modulation of Nucleus Accumbens Dopamine Release by Metabotropic Glutamate Receptors: Fast Cyclic Voltammetry Studies in Rat Brain Slices in Vitro.

ACS Chemical Neuroscience February 15, 2017 Ersin Yavas, Andrew M J Young

The N-methyl-d-aspartate (NMDA) receptor antagonist, phencyclidine, induces behavioral changes in rodents mimicking symptoms of schizophrenia, possibly mediated through dysregulation of glutamatergic control of mesolimbic dopamine release. We tested the hypothesis that NMDA receptor activation modulates accumbens dopamine release, and that phencyclidine pretreatment altered this modulation....

DOI: 10.1021/acschemneuro.6b00397 (opens in new tab) Full text (opens in new tab) Brain slices N-methyl-d-aspartate Dopamine Metabotropic glutamate receptors +2

5-HT2A/5-HT2C Receptor Pharmacology and Intrinsic Clearance of N-Benzylphenethylamines Modified at the Primary Site of Metabolism.

ACS Chemical Neuroscience November 16, 2016 Sebastian Leth-Petersen, Ida N Petersen, Anders A. Jensen et al.

The toxic hallucinogen 25B-NBOMe is very rapidly degraded by human liver microsomes and has low oral bioavailability. Herein we report on the synthesis, microsomal stability, and 5-HT2A/5-HT2C receptor profile of novel analogues of 25B-NBOMe modified at the primary site of metabolism. Although microsomal stability could be increased while maintaining potent 5-HT2 receptor agonist properties,...

DOI: 10.1021/acschemneuro.6b00265 (opens in new tab) Full text (opens in new tab) 5-ht2a receptor agonists Phenethylamines Hallucinogens Microsomal stability

N-Benzyl-5-methoxytryptamines as Potent Serotonin 5-HT2 Receptor Family Agonists and Comparison with a Series of Phenethylamine Analogues.

ACS Chemical Neuroscience July 15, 2015 David E Nichols, M Flori Sassano, Adam L. Halberstadt et al. 81 citations

A series of N-benzylated-5-methoxytryptamine analogues was prepared and investigated, with special emphasis on substituents in the meta position of the benzyl group. A parallel series of several N-benzylated analogues of 2,5-dimethoxy-4-iodophenethylamine (2C-I) also was included for comparison of the two major templates (i.e., tryptamine and phenethylamine). A broad affinity screen at...

Synthesis and structure-activity relationships of N-benzyl phenethylamines as 5-HT2A/2C agonists.

ACS Chemical Neuroscience March 19, 2014 Martin Hansen, Karina Phonekeo, James S Paine et al. 125 citations

N-Benzyl substitution of 5-HT2A receptor agonists of the phenethylamine structural class of psychedelics (such as 4-bromo-2,5-dimethoxyphenethylamine, often referred to as 2C-B) confer a significant increase in binding affinity as well as functional activity of the receptor. We have prepared a series of 48 compounds with structural variations in both the phenethylamine and N-benzyl part of the...

DOI: 10.1021/cn400216u (opens in new tab) Full text (opens in new tab) Receptor pharmacology Medicinal chemistry Serotonin receptors Drug discovery

Perspectives on zebrafish models of hallucinogenic drugs and related psychotropic compounds.

ACS Chemical Neuroscience August 6, 2013 Nikhil Neelkantan, Alina Mikhaylova, Adam Michael Stewart et al.

Among different classes of psychotropic drugs, hallucinogenic agents exert one of the most prominent effects on human and animal behaviors, markedly altering sensory, motor, affective, and cognitive responses. The growing clinical and preclinical interest in psychedelic, dissociative, and deliriant hallucinogens necessitates novel translational, sensitive, and high-throughput in vivo models and...

Extensive rigid analogue design maps the binding conformation of potent N-benzylphenethylamine 5-HT2A serotonin receptor agonist ligands.

ACS Chemical Neuroscience January 16, 2013 Jose I Juncosa, Martin Hansen, Lisa A Bonner et al.

Based on the structure of the superpotent 5-HT(2A) agonist 2-(4-bromo-2,5-dimethoxyphenyl)-N-[(2-methoxyphenyl)methyl]ethanamine, which consists of a ring-substituted phenethylamine skeleton modified with an N-benzyl group, we designed and synthesized a small library of constrained analogues to identify the optimal arrangement of the pharmacophoric elements of the ligand. Structures consisted...

Animal Models of Serotonergic Psychedelics

ACS Chemical Neuroscience September 24, 2012 James B. Hanks, Javier González-Maeso 152 citations

The serotonin 5-HT(2A) receptor is the major target of psychedelic drugs such as lysergic acid diethylamide (LSD), mescaline, and psilocybin. Serotonergic psychedelics induce profound effects on cognition, emotion, and sensory processing that often seem uniquely human. This raises questions about the validity of animal models of psychedelic drug action. Nonetheless, recent findings suggest...

Neonatal Citalopram Treatment Inhibits the 5-HT Depleting Effects of MDMA Exposure in Rats

ACS Chemical Neuroscience October 21, 2011 Tori L. Schaefer, Curtis E. Grace, Matthew R. Skelton et al. 5 citations

Neonatal exposure to 3,4-methylenedioxymethamphetamine (MDMA) produces long-term learning and memory deficits and increased anxiety-like behavior. The mechanism underlying these behavioral changes is unknown but we hypothesized that it involves perturbations to the serotonergic system as this is the principle mode of action of MDMA in the adult brain. During development 5-HT is a neurotrophic...