Hofer Katharina E, Faber Katrin, Müller Daniel M, Hauffe Till, Wenger Urs, Kupferschmidt Hugo, Rauber-Lüthy Christine
National Poisons Centre, Tox Info Suisse, Associated Institute of the University of Zurich, Zurich, Switzerland.
National Poisons Centre, Tox Info Suisse, Associated Institute of the University of Zurich, Zurich, Switzerland.
Ann Emerg Med. 2017 Jan;69(1):79-82. doi: 10.1016/j.annemergmed.2016.03.042. Epub 2016 May 4.
N-methyl-5-(2 aminopropyl)benzofuran (5-MAPB) is a novel psychoactive benzofuran, created by N-methylation of 5-(2-aminopropyl)benzofuran (5-APB), which shares structural features with methylenedioxymethamphetamine (MDMA). To our knowledge, no case of 5-MAPB-related toxicity has been published in the scientific literature. We report a case of oral 5-MAPB exposure confirmed by liquid chromatography-tandem mass spectrometry in a 24-year-old previously healthy white man. Observed symptoms and signs such as paleness, cold and clammy skin, hypertension, elevated high-sensitive troponin T level, tachycardia, ECG change, diaphoresis, mild hyperthermia, mydriasis, tremor, hyperreflexia, clonus, agitation, disorientation, hallucinations, convulsions, reduced level of consciousness, and creatine kinase level elevation (305 IU/L) were compatible with undesired effects related to 5-APB or MDMA exposure. Signs and symptoms resolved substantially within 14 hours with aggressive symptomatic treatment, including sedation with benzodiazepines, external cooling, analgesia and sedation with fentanyl-propofol, and treatment with urapidil, an α-receptor-blocking agent. 5-MAPB showed first-order elimination kinetics with a half-life of 6.5 hours, comparable to the half-life of MDMA. According to the chemical structure, this case report, and users' Web reports, 5-MAPB appears to have an acute toxicity profile similar to that of 5-APB and MDMA, with marked vasoconstrictor effect.
N-甲基-5-(2-氨基丙基)苯并呋喃(5-MAPB)是一种新型精神活性苯并呋喃,由5-(2-氨基丙基)苯并呋喃(5-APB)经N-甲基化产生,它与亚甲二氧基甲基苯丙胺(摇头丸)具有相似的结构特征。据我们所知,科学文献中尚未发表过与5-MAPB相关毒性的病例报告。我们报告了一例24岁既往健康的白人男性口服5-MAPB的病例,该病例经液相色谱-串联质谱法确诊。观察到的症状和体征,如面色苍白、皮肤冰冷潮湿、高血压、高敏肌钙蛋白T水平升高、心动过速、心电图改变、多汗、轻度体温升高、瞳孔散大、震颤、反射亢进、阵挛、躁动、定向障碍、幻觉、惊厥、意识水平降低以及肌酸激酶水平升高(305 IU/L),与5-APB或摇头丸暴露相关的不良反应相符。通过积极的对症治疗,包括使用苯二氮䓬类药物镇静、外部降温、使用芬太尼-丙泊酚镇痛和镇静以及使用α受体阻滞剂乌拉地尔治疗,症状和体征在14小时内基本缓解。5-MAPB呈现一级消除动力学,半衰期为6.5小时,与摇头丸的半衰期相当。根据化学结构、本病例报告以及使用者的网络报告,5-MAPB似乎具有与5-APB和摇头丸相似的急性毒性特征,具有明显的血管收缩作用。