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Serotonin: all studies

Page 375 of 400: studies 3,741 to 3,750 of 3,999, newest first. Back to the serotonin overview

Research

Application of electrophysiological method to study interactions between ibogaine and cocaine.

Annals of the New York Academy of Sciences September 1, 2000 Zbigniew Binienda, Michael A Beaudoin, Brett T Thorn et al. 4 citations

The psychoactive indole alkaloid, ibogaine (IBO), has been investigated for over a decade concerning its reported anti-addictive properties for opioids as well as psychomotor stimulants. The mechanism for the anti-addictive action of IBO is still unclear. IBO interactions with opioid, NMDA, nicotinic, adrenergic, and serotonergic receptor sites have been suggested. The involvement of the...

DOI: 10.1111/j.1749-6632.2000.tb05212.x (opens in new tab) Full text (opens in new tab) Ibogaine pretreatment Alter brain's reaction Dampens response Cocaine-induced +7

Agony and ecstasy: a review of MDMA effects and toxicity

European Psychiatry August 1, 2000 C. Burgess, Alan O'Donohoe, Michael Gill 108 citations

Summary Background Background – Ecstasy is a recreational drug with an anecdotal reputation for safety. However, reports of adverse effects and fatalities have increased in the medical and popular press. Methods Method – Literature search and review. Results Results – Acute Ecstasy toxicity does not appear to be due to overdose and cannot be solely attributed to the nature of the usual ambient...

N-methyl-1-(1,3-benzodioxol-5-yl)-2-butanamine (MBDB): its properties and possible risks.

Addiction Biology July 1, 2000 L A Aerts, M Mallaret, H Rigter 12 citations

Abstract MBDB (N -methyl-1-(1,3-benzodioxol-5-yl)-2-aminobutane) is the alpha-ethyl homologue of MDMA (3,4-methylenedioxy-N-methylamphetamine). MBDB is metabolized and excreted similarly to MDMA: presumably, the majority of oral MBDB is excreted in urine unmetabolized.The main metabolic routes in man are thought to be O-dealkylation and subsequent methylation, sulphation and glucuronidation of...

Antagonism of a PCP drug discrimination by hallucinogens and related drugs.

Neuropsychopharmacology June 2000 W B West, A Lou, K Pechersky et al.

Drugs such as PCP and MK-801 can cause psychotic reactions in humans by antagonizing NMDA receptors. This action is ultimately toxic to certain cortical neurons and may be one mechanism underlying neurodegenerative diseases, including schizophrenia. It has been reported that hallucinogens such as LSD, DOM, and DOI can block the neurotoxic effects of NMDA antagonists, possibly by activating...

Fluoxetine prevents PCP- and MK801-induced HSP70 expression in injured limbic cortical neurons of rats.

Biological Psychiatry May 1, 2000 M Tomitaka, S Tomitaka, S Rajdev et al.

N-Methyl-D-aspartate (NMDA) receptor antagonists, including phencyclidine (PCP) and dizocilpine (MK801), cause schizophrenialike psychosis in humans, and produce vacuolated neurons in the cingulate and retrosplenial cortices of the rat brain. Since psychotically depressed patients and schizophrenic depressed patients may require treatment with selective serotonin reuptake inhibitors (SSRIs), it...

Dysfunctional brain dopamine systems induced by psychotomimetic NMDA-receptor antagonists and the effects of antipsychotic drugs.

Brain research. Brain research reviews March 1, 2000 T H Svensson

Clinical studies utilizing imaging techniques demonstrate that classical antipsychotic drugs, such as haloperidol, in clinically effective doses display around 75% dopamine (DA)-D(2) receptor occupancy in the brain. In contrast, the atypical antipsychotic drug clozapine is even more effective at only about 45% D(2)-receptor occupancy. Yet at this D(2)-receptor occupancy classical antipsychotics...

‘Is MDMA a Human Neurotoxin?’:Diverse Views from the Discussants

Neuropsychobiology 2000 John Turner, A. C. Parrott 27 citations

UNLABELLED: Every discussant at the Novartis symposium was invited to submit a 250-word abstract, giving their views upon the question: 'Is MDMA a human neurotoxin?'. These abstracts are presented here. They illustrate a wide range of viewpoints and opinions, as might be expected from experts in such diverse fields: animal neuroscience, human cognitive testing, police pathology laboratory,...

Neurotropic Effect of Extracts from the Hallucinogenic Mushroom Psilocybe cubensis (Earle) Sing. (Agaricomycetideae). In Vitro Studies

International journal of medicinal mushrooms 2000 M. G. Moldavan, Elvira F. Solomko, Anna A. Grodzínskaya et al. 3 citations

The neurotropic effect of Psilocybe cubensis (Earle) Sing, dried biomass and fruiting bodies containing the indole hallucinogens psilocybin and psilocine on spike activity of pyramidal neurons from the rat hippocampal CAl region slices has been studied. Extracellularly responses of 50 neurons were recorded, 34 during the application of biomass extract (BME) and 16 during the application of...

DOI: 10.1615/intjmedmushr.v2.i4.130 (opens in new tab) Psilocybin Hippocampal formation Pharmacology Hallucinogen

Development of novel medications for drug addiction. The legacy of an African shrub.

Annals of the New York Academy of Sciences 2000 Stanley D Glick, Isabelle M Maisonneuve 64 citations

Ibogaine, one of several alkaloids found in the root bark of the African shrub Tabernanthe iboga, has been claimed to be effective in treating multiple forms of drug abuse. Problems associated with side effects of ibogaine have spawned a search for more effective and safer structural derivatives. 18-Methoxycoronaridine (18-MC), a novel iboga alkaloid congener, appears to have substantial...

DOI: 10.1111/j.1749-6632.2000.tb06677.x (opens in new tab) Full text (opens in new tab) Substance use disorder Addiction treatment Anti-addiction therapy Substance abuse treatment +20

Bufotenine: toward an understanding of possible psychoactive mechanisms.

Journal of Psychoactive Drugs 2000 M C Mcbride 71 citations

A review of the neuropharmacology of the alleged hallucinogen bufotenine is presented, including recent experimental results showing activity similar to LSD and other known hallucinogens (psilocin and 5-MeO-DMT) at the purported hallucinogenic serotonin (5-HT) receptors, 5-HT2A and 5-HT2C. In addition, current reports of computer modeling of the receptors and ligand binding sites give evidence...