CYP2D6 increases toxicity of the designer drug 4-methylthioamphetamine (4-MTA)

Toxicology

Volumn 229, Issue 3, 2007, Pages 236-244

  Carmo, Helena ^a   Brulport, Marc ^b   Hermes, Matthias ^b   Oesch, Franz ^c   de Boer, Douwe ^d   Remião, Fernando ^a   Carvalho, Félix ^a   Schön, Michael R ^b   Krebsfaenger, Niels ^e   Doehmer, Johannes ^f   Bastos, Maria de Lourdes ^a   Hengstler, Jan G ^b  

^a Rua do Campo Alegre s n   (Portugal)

^b UNIVERSITY OF LEIPZIG   (Germany)

^c JOHANNES GUTENBERG UNIVERSITY   (Germany)

^d MAASTRICHT UNIVERSITY MEDICAL CENTER   (Netherlands)

^e Schwarz Pharma AG   (Germany)

^f GenPharmTox BioTech AG   (Germany)

Author keywords

4 Methylthioamphetamine; CYP2D6; Designer drugs; Hepatotoxicity; Metabolism; Polymorphism

Indexed keywords

4 METHYLTHIOAMPHETAMINE; AMPHETAMINE DERIVATIVE; CYTOCHROME P450 2D6; CYTOCHROME P450 3A4; DESIGNER DRUG; ISOENZYME;

ALLELE; ANIMAL CELL; ARTICLE; CHINESE HAMSTER; COLONY FORMATION; COMPARATIVE STUDY; CONTROLLED STUDY; CYTOTOXICITY; GENE; GENE EXPRESSION; GENETIC SUSCEPTIBILITY; HUMAN; HUMAN CELL; LUNG FIBROBLAST; NONHUMAN; PRIORITY JOURNAL; WILD TYPE;

AMPHETAMINES; ANIMALS; CELL LINE; CELL SURVIVAL; CRICETINAE; CRICETULUS; CYTOCHROME P-450 CYP2D6; CYTOCHROME P-450 CYP3A; DESIGNER DRUGS; GENOTYPE;

CRICETULUS GRISEUS;

EID: 33845580694     PISSN: 0300483X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tox.2006.10.024     Document Type: Article

References (63)

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