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Mechanisms of MDMA (ecstasy)-induced oxidative stress, mitochondrial dysfunction, and organ damage.

Current pharmaceutical biotechnology
August 1, 2010
Byoung-Joon Song et al. (5 authors)
Journal ArticleResearch Support, N.I.H., IntramuralReviewAnimal Study
Study Details

Study Goal

The researchers aimed to update the understanding of MDMA-mediated organ damage mechanisms, focusing on oxidative modifications of mitochondrial proteins and mitochondrial dysfunction.

Results Summary

The study highlights MDMA-induced oxidative/nitrosative stress leading to mitochondrial dysfunction and organ damage, and introduces a proteomics method to identify oxidized proteins in MDMA-exposed rats. It also discusses synergistic drug interactions between MDMA and other substances like ethanol.

Population

Rats (animal study)

Effective Dosage

Not specified

Duration

Not specified

Interactions

Synergistic interactions with alcohol (ethanol) and other abused substances mentioned.

Extracted Claims (8)
InterventionDirectionEndpointPopulationDosageImpactClaim #
MDMA (3,4-methylenedioxymethamphetamine, ecstasy)
increase
acute and sub-chronic toxicities
-
-
caused
#1
MDMA (3,4-methylenedioxymethamphetamine, ecstasy)
increase
organ damage
-
-
mediated
#2
MDMA (3,4-methylenedioxymethamphetamine, ecstasy)
increase
oxidative/nitrosative stress
-
-
mediated
#3
MDMA (3,4-methylenedioxymethamphetamine, ecstasy)
increase
oxidative-modifications of mitochondrial proteins
-
-
leading to
#4
MDMA (3,4-methylenedioxymethamphetamine, ecstasy)
increase
mitochondrial dysfunction
-
-
leading to
#5
MDMA (3,4-methylenedioxymethamphetamine, ecstasy)
increase
oxidatively-modified mitochondrial proteins
rats
-
exposed
#6
MDMA (3,4-methylenedioxymethamphetamine, ecstasy)
increase
organ damage
-
-
synergistic drug-interaction between
#7
MDMA (3,4-methylenedioxymethamphetamine, ecstasy) and other abused substances including alcohol (ethanol)
increase
organ damage
-
-
synergistic drug-interaction
#8
Abstract

Despite numerous reports about the acute and sub-chronic toxicities caused by MDMA (3,4-methylenedioxymethamphetamine, ecstasy), the underlying mechanism of organ damage is poorly understood. The aim of this review is to present an update of the mechanistic studies on MDMA-mediated organ damage partly caused by increased oxidative/nitrosative stress. Because of the extensive reviews on MDMA-mediated oxidative stress and tissue damage, we specifically focus on the mechanisms and consequences of oxidative-modifications of mitochondrial proteins, leading to mitochondrial dysfunction. We briefly describe a method to systematically identify oxidatively-modified mitochondrial proteins in control and MDMA-exposed rats by using biotin-N-maleimide (biotin-NM) as a sensitive probe for oxidized proteins. We also describe various applications and advantages of this Cys-targeted proteomics method and alternative approaches to overcome potential limitations of this method in studying oxidized proteins from MDMA-exposed tissues. Finally we discuss the mechanism of synergistic drug-interaction between MDMA and other abused substances including alcohol (ethanol) as well as application of this redox-based proteomics method in translational studies for developing effective preventive and therapeutic agents against MDMA-induced organ damage.

Medical Subject Headings (MeSH)
AnimalsHallucinogensHumansMitochondriaModels, BiologicalMultiple Organ FailureN-Methyl-3,4-methylenedioxyamphetamineOxidative StressRatsViscera
Study Links
Quality Scores
Safety20
Quality75/10
Citation Metrics
Total Citations46
Citations/Year3.1
Relative Citation Ratio1.54
NIH Percentile66%
Research Impact Scores
APT Score0.25
Weight Score0.64
Normalized Score0.43
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