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Serotonin: all studies

Page 161 of 407: studies 1,601 to 1,610 of 4,066, newest first. Back to the serotonin overview

Research

Comparative Effects of Substituted Amphetamines (PMA, MDMA, and METH) on Monoamines in Rat Caudate

Annals of the New York Academy of Sciences June 1, 2002 B. Gough, Syed Z. Imam, Bruce E. Blough et al. 47 citations

A bstract : Paramethoxyamphetamine (PMA) is a methoxylated phenethylamine derivative that has been used illicitly in Australia since 1994. PMA is also becoming popular at rave parties in the United States. PMA raised concern when a series of fatalities resulted after its use in South Australia, where it was marketed as “ecstasy,” which is the colloquial name for MDMA. In the present study, we...

A Single Dose of Lysergic Acid Diethylamide Influences Gene Expression Patterns within the Mammalian Brain

Neuropsychopharmacology May 1, 2002 C Nichols 165 citations

Hallucinogenic drugs such as lysergic acid diethylamide (LSD) have profound effects on humans including hallucinations and detachment from reality. These remarkable behavioral effects have many similarities to the debilitating symptoms of neuropsychiatric disorders such as schizophrenia. The effects of hallucinogens are thought to be mediated by serotonin receptor activation; however, how these...

Behavioral Psychopharmacology of MDMA and MDMA-Like Drugs: A Review of Human and Animal Studies

Addiction Research & Theory 2002 Diana L. Martinez-Price, Kirsten Krebs-Thomson, Mark A. Geyer 16 citations

Since being classified as a Schedule I controlled substance, MDMA (3,4-methylenedioxy-N-methylamphetamine; "ecstasy") has been the subject of controversy regarding its potential therapeutic usage, increased use by young people in the "Rave" culture, and issues of potential neurotoxicity. This review article summarizes much of the animal and human studies of the general behavioral effects of...

Long-Term Neuropsychiatric Consequences of "Ecstasy" (MDMA): A Review

Harvard Review of Psychiatry 2002 Alonso Montoya, Renée Sorrentino, Scott E Lukas et al. 102 citations

The recreational drug "ecstasy" (3,4-methylenedioxymethamphetamine, or MDMA) is widely used by young people throughout the world. Experimental studies indicate that MDMA damages serotonergic neurons in animals and possibly in humans. Repeated use may induce long-term neurotoxic effects, with cognitive and behavioral implications. We reviewed both the preclinical and the clinical literature to...

The pharmacology of the acute hyperthermic response that follows administration of 3,4‐methylenedioxymethamphetamine (MDMA, ‘ecstasy’) to rats

British Journal of Pharmacology 2002 Annis O. Mechan, B. Moreno Esteban, Esther O’shea et al. 219 citations

The pharmacology of the acute hyperthermia that follows 3,4‐methylenedioxymethamphetamine (MDMA, ‘ecstasy’) administration to rats has been investigated. MDMA (12.5 mg kg −1 i.p.) produced acute hyperthermia (measured rectally). The tail skin temperature did not increase, suggesting that MDMA may impair heat dissipation. Pretreatment with the 5‐HT 1/2 antagonist methysergide (10 mg kg −1 ), the...

Effects of the Hallucinogen Psilocybin on Covert Orienting of Visual Attention in Humans

Neuropsychobiology 2002 Euphrosyne Gouzoulis‐mayfrank, B. Thelen, Stefanie Maier et al. 69 citations

Hallucinogenic drug-induced states are considered as models for acute schizophrenic disorders (experimental psychoses). In a double-blind study with healthy volunteers we investigated the influence of the serotonergic hallucinogen psilocybin, the ecstasy-like drug 3,4-methylenedioxyethylamphetamine (MDE), the stimulant d- methamphetamine and placebo on covert orienting of spatial attention (n =...

Brain mechanisms of hallucinogens and entactogens

Dialogues in Clinical Neuroscience December 31, 2001 Franz X. Vollenweider 127 citations

This review focuses on recent brain imaging and behavioral studies of sensory gating functions, which assess similarities between the effects of classic hallucinogens (eg, psilocybin), dissociative anesthetics (eg, ketamine), and entactogens (eg, 3,4-methylenedioxymethamphetamine [MDMA]) in humans. Serotonergic hallucinogens and psychotomimetic anesthetics produce overlapping psychotic...

A Comprehensive Review of MDMA and GHB: Two Common Club Drugs

Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy December 1, 2001 Christian J. Teter, Sally K. Guthrie 114 citations

“Club drugs” have become alarmingly popular. The use of 3,4‐methylenedioxymethamphetamine (MDMA, Ecstasy) and γ‐hydroxybutyrate (GHB), in particular, has increased dramatically from 1997–1999. The pharmacokinetics of MDMA and GHB appear to be nonlinear, making it difficult to estimate a dose‐response relationship. The drug MDMA is an amphetamine analog with sympathomimetic properties, whereas...

DOI: 10.1592/phco.21.20.1486.34472 (opens in new tab) MDMA Ecstasy Rhabdomyolysis Gamma hydroxybutyrate +11

Which neuroreceptors mediate the subjective effects of MDMA in humans? A summary of mechanistic studies

Human Psychopharmacology: Clinical and Experimental December 1, 2001 Matthias E. Liechti, Franz X. Vollenweider 243 citations

Abstract In preclinical studies, 3,4‐methylenedioxymethamphetamine (MDMA, ‘Ecstasy’) has been shown to release serotonin (5‐HT), dopamine and norepinephrine. However, the role of these neurotransmitters and their corresponding receptor sites in mediating the subjective effects of MDMA has not yet been studied in humans. Therefore, we investigated the effects of three different neuroreceptor...

Human psychopharmacology of Ecstasy (MDMA): a review of 15 years of empirical research

Human Psychopharmacology: Clinical and Experimental December 1, 2001 A. C. Parrott 349 citations

Abstract MDMA (3,4‐methylenedioxymethamphetamine) or ‘Ecstasy’ was scheduled as an illegal drug in 1986, but since then its recreational use has increased dramatically. This review covers 15 years of research into patterns of use, its acute psychological and physiological effects, and the long‐term consequences of repeated use. MDMA is an indirect monoaminergic agonist, stimulating the release...