Mechanisms of MDMA (Ecstasy)-Induced Oxidative Stress, Mitochondrial Dysfunction, and Organ Damage

被引:44
作者
Song, Byoung-Joon [1 ]
Moon, Kwan-Hoon [1 ]
Upreti, Vijay V. [2 ]
Eddington, Natalie D. [2 ]
Lee, Insong J. [3 ]
机构
[1] NIAAA, Lab Membrane Biochem & Biophys, Bethesda, MD 20892 USA
[2] Univ Maryland, Sch Pharm, Dept Pharmaceut Sci, Baltimore, MD 21201 USA
[3] Coll Notre Dame Maryland, Sch Pharm, Dept Pharmaceut Sci, Baltimore, MD 21210 USA
关键词
MDMA; metabolism; oxidative/nitrosative stress; protein oxidation; functional redox proteomics; mitochondrial dysfunction; organ damage; ALCOHOLIC FATTY LIVER; CULTURED RAT HEPATOCYTES; NITRIC-OXIDE; 3,4-METHYLENEDIOXYMETHAMPHETAMINE ECSTASY; ALDEHYDE DEHYDROGENASE; GEL-ELECTROPHORESIS; REACTIVE OXYGEN; SEROTONERGIC NEUROTOXICITY; TRYPTOPHAN-HYDROXYLASE; PROTEIN MODIFICATIONS;
D O I
10.2174/138920110791591436
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:434 / 443
页数:10
相关论文
共 107 条
[1]   Role of peroxisome proliferator-activated receptor-α in fasting-mediated oxidative stress [J].
Abdelmegeed, Mohamed A. ;
Moon, Kwan-Hoon ;
Hardwick, James P. ;
Gonzalez, Frank J. ;
Song, Byoung-Joon .
FREE RADICAL BIOLOGY AND MEDICINE, 2009, 47 (06) :767-778
[2]   Single exposure to cocaine or ecstasy induces DNA damage in brain and other organs of mice [J].
Alvarenga, Tathiana A. ;
Andersen, Monica L. ;
Ribeiro, Daniel A. ;
Araujo, Paula ;
Hirotsu, Camila ;
Costa, Jose L. ;
Battisti, Murilo C. ;
Tufik, Sergio .
ADDICTION BIOLOGY, 2010, 15 (01) :96-99
[3]   ACETYL-L-CARNITINE PROVIDES EFFECTIVE IN VIVO NEUROPROTECTION OVER 3,4-METHYLENEDIOXIMETHAMPHETAMINE-INDUCED MITOCHONDRIAL NEUROTOXICITY IN THE ADOLESCENT RAT BRAIN [J].
Alves, E. ;
Binienda, Z. ;
Carvalho, F. ;
Alves, C. J. ;
Fernandes, E. ;
Bastos, M. De Lourdes ;
Tavares, M. A. ;
Summavielle, T. .
NEUROSCIENCE, 2009, 158 (02) :514-523
[4]   Drug-associated mitochondrial toxicity and its detection [J].
Amacher, DE .
CURRENT MEDICINAL CHEMISTRY, 2005, 12 (16) :1829-1839
[5]   Ecstasy:: a common cause of severe acute hepatotoxicity [J].
Andreu, V ;
Mas, A ;
Bruguera, MB ;
Salmerón, JM ;
Moreno, V ;
Nogué, S ;
Rodés, J .
JOURNAL OF HEPATOLOGY, 1998, 29 (03) :394-397
[6]   Inactivation of tyrosine hydroxylase by nitration following exposure to peroxynitrite and 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) [J].
Ara, J ;
Przedborski, S ;
Naini, AB ;
Jackson-Lewis, V ;
Trifiletti, RR ;
Horwitz, J ;
Ischiropoulos, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (13) :7659-7663
[7]   CDNA-DERIVED AMINO-ACID-SEQUENCE OF RAT MITOCHONDRIAL 3-OXOACYL-COA THIOLASE WITH NO TRANSIENT PRESEQUENCE - STRUCTURAL RELATIONSHIP WITH PEROXISOMAL ISOZYME [J].
ARAKAWA, H ;
TAKIGUCHI, M ;
AMAYA, Y ;
NAGATA, S ;
HAYASHI, H ;
MORI, M .
EMBO JOURNAL, 1987, 6 (05) :1361-1366
[8]   Serotonergic neurotoxicity of 3,4-(±) -methylenedioxyamphetamine and 3,4-(±)-methylendioxymethamphetamine (ecstasy) is potentiated by inhibition of γ-glutamyl transpeptidase [J].
Bai, FJ ;
Jones, DC ;
Lau, SS ;
Monks, TJ .
CHEMICAL RESEARCH IN TOXICOLOGY, 2001, 14 (07) :863-870
[9]   Chronic exposure to MDMA (ecstasy) increases DNA damage in sperm and alters testes histopathology in male rats [J].
Barenys, Marta ;
Macia, Nuria ;
Camps, Lydia ;
de Lapuente, Joaquin ;
Gomez-Catalan, Jesus ;
Gonzalez-Linares, Javier ;
Borras, Miquel ;
Rodamilans, Miguel ;
Llobet, Juan M. .
TOXICOLOGY LETTERS, 2009, 191 (01) :40-46
[10]   Patterns of simultaneous polysubstance use in drug using university students [J].
Barrett, Sean P. ;
Darredeau, Christine ;
Pihl, Robert O. .
HUMAN PSYCHOPHARMACOLOGY-CLINICAL AND EXPERIMENTAL, 2006, 21 (04) :255-263