Department of Pharmacology and Experimental Therapeutics and Cardiovascular Center, Louisiana State University Health Sciences Center, New Orleans, LA 70112, USA.
Curr Pharm Biotechnol. 2010 Aug;11(5):470-5. doi: 10.2174/138920110791591526.
The recreational use of 3, 4 methylenedioxymethamphetamine (ecstasy or MDMA) has increased dramatically over the past thirty years due to its ability to increase stamina and produce feelings of emotional closeness and wellbeing. In spite of the popular perception that MDMA is a safe drug, there is a large literature documenting that the drug can produce significant neurotoxicity, especially in serotonergic and catecholaminergic systems. There are also experimental and clinical data which document that MDMA can alter cardiovascular function and produce cardiac toxicity, including rhythm disturbances, infarction and sudden death. This manuscript will review the literature documenting the cardiovascular responses elicited by MDMA in humans and experimental animals and will examine the underlying mechanisms mediating these responses. We will also review the available clinical, autopsy and experimental data linking MDMA with cardiac toxicity. Most available data indicate that oxidative stress plays an important role in the cardiotoxic actions of MDMA. Moreover, new data indicates that redox active metabolites of MDMA may play especially important roles in MDMA induced toxicity.
过去三十年来,3,4-亚甲基二氧甲基苯丙胺(摇头丸或 MDMA)的娱乐性使用急剧增加,因为它能够提高耐力并产生情感亲近和幸福感。尽管人们普遍认为 MDMA 是一种安全的药物,但大量文献记录表明该药物会产生显着的神经毒性,特别是在血清素能和儿茶酚胺能系统中。也有实验和临床数据记录表明,MDMA 可改变心血管功能并产生心脏毒性,包括心律紊乱、梗塞和猝死。本文将回顾记录 MDMA 在人类和实验动物中引起的心血管反应的文献,并研究介导这些反应的潜在机制。我们还将回顾将 MDMA 与心脏毒性联系起来的现有临床、尸检和实验数据。大多数现有数据表明,氧化应激在 MDMA 的心脏毒性作用中发挥重要作用。此外,新数据表明,MDMA 的氧化还原活性代谢物可能在 MDMA 诱导的毒性中发挥特别重要的作用。