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Toxicity of ecstasy (MDMA) towards embryonic stem cell-derived cardiac and neural cells.

Rokhsareh Meamar, Fereshteh Karamali, Hamid Mirmohamad Sadeghi, Mahmood Etebari, Mohammad Hossein Nasr-Esfahani, Hossein Baharvand

Toxicology in Vitro June 2010 DOI: 10.1016/j.tiv.2010.03.005 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics In vitro experimental study Peer reviewed
Population Mouse embryonic stem cell-derived embryoid bodies
Intervention MDMA
Measures MAP2
Topics MDMA
Key findings MDMA reduced beating cardiomyocytes and neurons in mouse embryonic stem cell cultures, with neural differentiation more strongly affected than cardiac differentiation. The authors classify MDMA as a moderate or weak teratogen based on their linear discriminate function, and report a lower ID50 for neural cell morphology than for cardiac cells.

Abstract

"Ecstasy" or methylenedioxymethamphetamine (MDMA) is primarily a recreational drug commonly used during the child bearing period, thus, there is a major concern regarding the embryonic and fetal toxicity of this drug. Here, we report the cardio- and neuro-toxic effects of MDMA on beating embryoid bodies (EBs) and neural cell-containing EBs derived from mouse embryonic stem cell (ESCs). Based on our linear discriminate function, MDMA is considered to be a moderate or weak teratogen. Moreover, the generation of EBs with neural cell morphology and the expression of MAP2, a mature neuron marker, decrease more when MDMA is administered during the EB formation stage rather than post-plated EBs. In addition, the ID50 (inhibition of differentiation) of EBs with neural cell morphology is less than cardiac cells. In conclusion, MDMA causes a marked reduction in beating cardiomyocytes and neurons in ESC cultures, and this drug has a more potent toxicity on neural rather than cardiac cell differentiation.

Comparable studies

Other preclinical and animal studies on MDMA, most cited first.

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