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Helena Carmo

10 papers in the library · 117 citations · publishing 2004-2026

Papers

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Psilocybin and Psilocybe cubensis extract exhibit divergent behavioural and toxicological effects in rats

Science Letters April 17, 2026 Diana Dias Da Silva, Andreia Machado Brito-Da-Costa, Francisco Sacadura et al.

Background: Psilocybin, a key psychoactive compound found in Psilocybe mushrooms, has gained increasing attention due to its therapeutic potential in neuropsychiatric disorders [1]. However, comparative preclinical data between isolated psilocybin and whole mushroom extracts remain scarce, particularly regarding behavioural reinforcement and peripheral toxicity [2,3]. Objective: To compare the...

DOI: 10.48797/sl.2026.497 (opens in new tab) Psilocybin Lipid peroxidation Analysis of variance Peripheral +3

Impact of psilocybin and Psilocybe cubensis extract on gut microbiota in Wistar Han rats

Science Letters April 17, 2026 Francisco Sacadura, Cláudia Marques, Andreia Machado Brito-Da-Costa et al.

Background: Psilocybin, the main psychoactive compound found in Psilocybe mushrooms, has gained increasing attention due to its potential therapeutic effects in neuropsychiatric disorders [1]. Beyond its central effects, increasing evidence highlights the relevance of the gut–brain axis, suggesting that psychedelics may also influence intestinal microbiota composition. Whole mushroom extracts...

DOI: 10.48797/sl.2026.492 (opens in new tab) Psilocybin Gut flora Amplicon sequencing Mushroom +5

Synthetic Cannabinoids: A Pharmacological and Toxicological Overview.

The Annual Review of Pharmacology and Toxicology August 1, 2022 R. Roque-Bravo, Rafaela Sofia Silva, R. Malheiro et al.

Synthetic cannabinoids (SCs) are a chemically diverse group of new psychoactive substances (NPSs) that target the endocannabinoid system, triggering a plethora of actions (e.g., elevated mood sensation, relaxation, appetite stimulation) that resemble, but are more intense than, those induced by cannabis. Although some of these effects have been explored for therapeutic applications, anticipated...

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

Mixtures of 3,4‐methylenedioxymethamphetamine (ecstasy) and its major human metabolites act additively to induce significant toxicity to liver cells when combined at low, non‐cytotoxic concentrations

Journal of Applied Toxicology June 1, 2014 Diana Dias Da Silva, Elisabete Silva, Félix Carvalho et al.

ABSTRACT: Hepatic injury after 3,4‐methylenedioxymethamphetamine (MDMA; ecstasy) intoxications is highly unpredictable and does not seem to correlate with either dosage or frequency of use. The mechanisms involved include the drug metabolic bioactivation and the hyperthermic state of the liver triggered by its thermogenic action and exacerbated by the environmental circumstances of abuse at hot...

Metabolic interactions between ethanol and MDMA in primary cultured rat hepatocytes.

Toxicology April 11, 2010 Helena Pontes, Paula Guedes de Pinho, Eduarda Fernandes et al.

3,4-Methylenedioxymethamphetamine (MDMA; ecstasy), a drug of abuse commonly consumed at rave parties, is often taken in a polydrug abuse scenario, ethanol being one of the most associated drugs. Both MDMA and ethanol are mainly metabolized in the liver with formation of toxic metabolites. Our working hypothesis is that ethanol can modify the metabolism of MDMA through the cytochrome P450...

Molecular and Cellular Mechanisms of Ecstasy-Induced Neurotoxicity: An Overview

Molecular Neurobiology June 1, 2009 João Paulo Capela, Helena Carmo, Fernando Remião et al.

“Ecstasy” [(±)-3,4-methylenedioxymethamphetamine, MDMA, XTC, X, E] is a psychoactive recreational hallucinogenic substance and a major worldwide drug of abuse. Several reports raised the concern that MDMA has the ability to induce neurotoxic effects both in laboratory animals and humans. Despite more than two decades of research, the mechanisms by which MDMA is neurotoxic are still to be fully...

Synergistic toxicity of ethanol and MDMA towards primary cultured rat hepatocytes.

Toxicology December 5, 2008 Helena Pontes, Carla Sousa, Renata Silva et al.

Ethanol is frequently consumed along with 3,4-methylenedioxymethamphetamine (MDMA; ecstasy). Since both compounds are hepatotoxic and are metabolized in the liver, an increased deleterious interaction resulting from the concomitant use of these two drugs seems plausible. Another important feature of MDMA-induced toxicity is hyperthermia, an effect known to be potentiated after continuous...

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