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Maria de Lourdes Bastos

16 papers in the library · 593 citations · publishing 2004-2024

Papers

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UTILIZAÇÃO DE PSICODÉLICOS NO TRANSTORNO DEPRESSIVO REFRATÁRIO: UMA REVISÃO DE LITERATURA

Revista CPAQV - Centro de Pesquisas Avançadas em Qualidade de Vida October 4, 2024 Claudio Mateus Gnoatto, Keyla Liana Bezerra Machado, Rian Ricardo Henrique da Silva et al.

Introdução: O Transtorno Depressivo Maior (TDM) é altamente prevalente e incapacitante, ocupando um alto ônus globalmente. No Brasil, afeta 15,5% da população. A fisiopatologia da depressão envolve teorias, incluindo a monoaminérgica e a dos receptores monoaminérgicos, embora nenhuma seja conclusiva. Tratamentos farmacológicos baseiam-se na teoria monoaminérgica, apesar de suas limitações. Além...

Ecstasy metabolites and monoamine neurotransmitters upshift the Na+/K+ ATPase activity in mouse brain synaptosomes.

Archives of Toxicology December 2022 Daniel José Barbosa, João Paulo Capela, Luísa Maria Ferreira et al.

3,4-Methylenedioximethamphetamine (MDMA; "ecstasy") is a psychotropic drug with well-known neurotoxic effects mediated by hitherto not fully understood mechanisms. The Na+- and K+-activated adenosine 5'-triphosphatase (Na+/K+ ATPase), by maintaining the ion gradient across the cell membrane, regulates neuronal excitability. Thus, a perturbation of its function strongly impacts cell homeostasis,...

DOI: 10.1007/s00204-022-03370-7 (opens in new tab) Full text (opens in new tab) 3,4-Methylenedioxymethamphetamine MDMA MDMA Brain Effects MDMA Metabolites Monoamine neurotransmitters +2

Drinking to death: Hyponatraemia induced by synthetic phenethylamines.

Drug and Alcohol Dependence July 1, 2020 Ana Carolina Faria, Helena Carmo, Félix Carvalho et al.

Synthetic phenethylamines are widely abused drugs, comprising new psychoactive substances such as synthetic cathinones, but also well-known amphetamines such as methamphetamine and 3,4-methylenedioxymethamphetamine (MDMA, ecstasy). Cathinones and amphetamines share many toxicodynamic mechanisms. One of their potentially life-threatening consequences, particularly of MDMA, is serotonin-mediated...

DOI: 10.1016/j.drugalcdep.2020.108045 (opens in new tab) Full text (opens in new tab) 3,4-Methylenedioxymethamphetamine MDMA, Ecstasy Serotonin syndrome Synthetic cathinone

GC-MS metabolomics reveals disturbed metabolic pathways in primary mouse hepatocytes exposed to subtoxic levels of 3,4-methylenedioxymethamphetamine (MDMA).

Archives of Toxicology November 2018 Ana Margarida Araújo, Maria de Lourdes Bastos, Eduarda Fernandes et al.

3,4-Methylenedioxymethamphetamine (MDMA, ecstasy) is a well-known hepatotoxic drug. Although its toxicity has been thoroughly studied at high concentrations, there is still insufficient knowledge on possible alterations of cell function at subtoxic concentrations, which are in fact more representative concentrations of intoxication scenarios. In this study, a gas chromatography-mass...

DOI: 10.1007/s00204-018-2314-9 (opens in new tab) Full text (opens in new tab) MDMA Hepatotoxicity Metabolomics Primary mouse hepatocytes +1

The hallucinogenic world of tryptamines: an updated review.

Archives of Toxicology August 1, 2015 Ana Margarida Araújo, Félix Carvalho, Maria de Lourdes Bastos et al. 290 citations

In the area of psychotropic drugs, tryptamines are known to be a broad class of classical or serotonergic hallucinogens. These drugs are capable of producing profound changes in sensory perception, mood and thought in humans and act primarily as agonists of the 5-HT2A receptor. Well-known tryptamines such as psilocybin contained in Aztec sacred mushrooms and N,N-dimethyltryptamine (DMT),...

Analytical investigation of legal high products containing Salvia divinorum traded in smartshops and internet.

Forensic Science International September 1, 2014 Fernando Xavier Moreira, Félix Carvalho, Maria de Lourdes Bastos et al. 13 citations

Lately, the hallucinogenic plant Salvia divinorum has been considered a popular recreational product among adolescents, being legally sold in several countries in "smartshops" and in internet websites. Sellers frequently omit the safety information about the plant, encouraging its use for recreational purposes, without providing adequate qualitative and quantitative details. The principal...

MDMA impairs mitochondrial neuronal trafficking in a Tau- and Mitofusin2/Drp1-dependent manner.

Archives of Toxicology August 2014 Daniel José Barbosa, Roman Serrat, Serena Mirra et al.

Identification of the mechanisms by which drugs of abuse cause neuronal dysfunction is essential for understanding the biological bases of their acute and long-lasting effects in the brain. Here, we performed real-time functional experiments of axonal transport of mitochondria to explore the role of in situ mitochondrial dysfunction in 3,4-methylenedioxymethamphetamine (MDMA; "ecstasy")-related...

The mixture of "ecstasy" and its metabolites impairs mitochondrial fusion/fission equilibrium and trafficking in hippocampal neurons, at in vivo relevant concentrations.

Toxicological sciences : an official journal of the Society of Toxicology June 2014 Daniel José Barbosa, Roman Serrat, Serena Mirra et al.

3,4-Methylenedioxymethamphetamine (MDMA; "ecstasy") is a potentially neurotoxic recreational drug of abuse. Though the mechanisms involved are still not completely understood, formation of reactive metabolites and mitochondrial dysfunction contribute to MDMA-related neurotoxicity. Neuronal mitochondrial trafficking, and their targeting to synapses, is essential for proper neuronal function and...

DOI: 10.1093/toxsci/kfu042 (opens in new tab) Full text (opens in new tab) 3,4-Methylenedioxymethamphetamine MDMA MDMA'S Metabolites Mitochondrial dysfunction Mitochondrial fusion/fission +2

The neurotoxicity of hallucinogenic amphetamines in primary cultures of hippocampal neurons.

Neurotoxicology January 2013 João Paulo Capela, Silvana Da Costa Araújo, Vera Marisa Costa et al.

3,4-Methylenedioxymethamphetamine (MDMA or "Ecstasy") and 2,5-dimethoxy-4-iodoamphetamine hydrochloride (DOI) are hallucinogenic amphetamines with addictive properties. The hippocampus is involved in learning and memory and seems particularly vulnerable to amphetamine's neurotoxicity. We evaluated the neurotoxicity of DOI and MDMA in primary neuronal cultures of hippocampus obtained from Wistar...

Pro‐oxidant effects of Ecstasy and its metabolites in mouse brain synaptosomes

British Journal of Pharmacology April 21, 2011 Daniel José Barbosa, João Paulo Capela, Jorge M.A. Oliveira et al. 60 citations

BACKGROUND AND PURPOSE: 3,4-Methylenedioxymethamphetamine (MDMA or 'Ecstasy') is a worldwide major drug of abuse known to elicit neurotoxic effects. The mechanisms underlying the neurotoxic effects of MDMA are not clear at present, but the metabolism of dopamine and 5-HT by monoamine oxidase (MAO), as well as the hepatic biotransformation of MDMA into pro-oxidant reactive metabolites is thought...

Effect of 3,4-methylenedioxyamphetamine on dendritic spine dynamics in rat neocortical neurons--involvement of heat shock protein 27.

Brain Research January 25, 2011 Karsten Ruscher, Eduarda Fernandes, João Paulo Capela et al.

Along with chronic neurotoxic effects, the long-term consumption of amphetamines has been associated to psychiatric symptoms and memory disturbances. Dendritic spine dynamics have been discussed as a possible morphological correlate. However, the underlying mechanisms are still elusive. 3,4-Methylenedioxyamphetamine (MDA), a major drug of abuse and a main metabolite after...

Ecstasy-induced oxidative stress to adolescent rat brain mitochondria in vivo: influence of monoamine oxidase type A.

Addiction Biology April 2009 Ema Alves, Teresa Summavielle, Cecília Juliana Alves et al.

The administration of a neurotoxic dose of 3,4-methylenedioxymethamphetamine (MDMA; 'ecstasy') to the rat results in mitochondrial oxidative damage in the central nervous system, namely lipid and protein oxidation and mitochondrial DNA deletions with subsequent impairment of the correspondent protein expression. Although these toxic effects were shown to be prevented by monoamine oxidase B...

Synthesis and Cyclic Voltammetry Studies of 3,4-Methylenedioxymethamphetamine (MDMA) Human Metabolites

JOURNAL OF HEALTH SCIENCE 2007 Carla Macedo, Paula S. Branco, Luı́sa M. Ferreira et al. 36 citations

3,4-Methylenedioxymethamphetamine (MDMA or "Ecstasy") is a widely abused, psychoactive recreational drug. There are growing evidences that the MDMA neurotoxic profile may be highly dependent on its hepatic metabolism. MDMA metabolism leads to the production of highly reactive derivates, namely catechols, catechol thioethers, and quinones. In this study the electrochemical oxidation-reduction...

DOI: 10.1248/jhs.53.31 (opens in new tab) MDMA Ecstasy Cyclic voltammetry Catechol +3

Metabolic pathways of 4-bromo-2,5-dimethoxyphenethylamine (2C-B): analysis of phase I metabolism with hepatocytes of six species including human.

Toxicology January 5, 2005 Helena Carmo, Jan G Hengstler, Douwe De Boer et al. 85 citations

4-Bromo-2,5-dimethoxyphenethylamine (2C-B) is a psychoactive designer drug of abuse that is sold under the street names "Venus", "Bromo", "Erox", "XTC" or "Nexus". Concern has been raised because only little is known about its toxicity and metabolism in humans. In the present study we incubated 2C-B with human, monkey, dog, rabbit, rat and mouse hepatocytes to identify the metabolites formed...

DOI: 10.1016/j.tox.2004.07.004 (opens in new tab) Full text (opens in new tab) Drug metabolism Biotransformation Drug breakdown Drug processing +23

Metabolism of the designer drug 4-bromo-2,5-dimethoxyphenethylamine (2C-B) in mice, after acute administration.

Journal of Chromatography B November 25, 2004 Helena Carmo, Douwe De Boer, Fernando Remião et al. 32 citations

4-Bromo-2,5-dimethoxyphenethylamine (2C-B) is a psychoactive drug of abuse often sold under the general street name "Ecstasy". Recent reports on the abuse of 2C-B and analogues denote the lack of knowledge on this drug metabolism. In the present study, we investigated the metabolic profile of 2C-B in the mouse and found unchanged 2C-B and several metabolites, which could be identified by GC/MS...

DOI: 10.1016/j.jchromb.2004.08.026 (opens in new tab) Full text (opens in new tab) Drug metabolism Forensic toxicology Psychoactive drugs Animal studies

Metabolism Is Required for the Expression of Ecstasy-Induced Cardiotoxicity in Vitro

Chemical Research in Toxicology April 27, 2004 Márcia Carvalho, Fernando Remião, Nuno Milhazes et al. 77 citations

Cardiovascular complications associated with 3,4-methylenedioxymethamphetamine (MDMA, ecstasy) abuse have increasingly been reported. The indirect effect of MDMA mediated by a sustained high level of circulating biogenic amines may contribute to the cardiotoxic effects, but other factors, like the direct toxic effects of MDMA and its metabolites in cardiac cells, remain to be investigated....

DOI: 10.1021/tx049960f (opens in new tab) MDMA Ecstasy Glutathione reductase Pharmacology +6