Paillet-Loilier Magalie, Cesbron Alexandre, Le Boisselier Reynald, Bourgine Joanna, Debruyne Danièle
Toxicology and Pharmacology Laboratory, University Hospital Centre, Caen, France.
Centre d'Evaluation et d'Information sur la Pharmacodépendance - Addictovigilance (CEIP-A), Department of Pharmacology, University Hospital Centre, Caen, France.
Subst Abuse Rehabil. 2014 May 26;5:37-52. doi: 10.2147/SAR.S37257. eCollection 2014.
Substituted cathinones are synthetic analogs of cathinone that can be considered as derivatives of phenethylamines with a beta-keto group on the side chain. They appeared in the recreational drug market in the mid-2000s and now represent a large class of new popular drugs of abuse. Initially considered as legal highs, their legal status is variable by country and is rapidly changing, with government institutions encouraging their control. Some cathinones (such as diethylpropion or pyrovalerone) have been used in a medical setting and bupropion is actually indicated for smoking cessation. Substituted cathinones are widely available from internet websites, retail shops, and street dealers. They can be sold under chemical, evocative or generic names, making their identification difficult. Fortunately, analytical methods have been developed in recent years to solve this problem. Available as powders, substituted cathinones are self-administered by snorting, oral injestion, or intravenous injection. They act as central nervous system stimulants by causing the release of catecholamines (dopamine, noradrenaline, and serotonin) and blocking their reuptake in the central and peripheral nervous system. They may also decrease dopamine and serotonin transporter function as nonselective substrates or potent blockers and may inhibit monoamine oxidase effects. Nevertheless, considerable differences have been found in the potencies of the different substituted cathinones in vitro. Desired effects reported by users include increased energy, empathy, and improved libido. Cardiovascular (tachycardia, hypertension) and psychiatric/neurological signs/symptoms (agitation, seizures, paranoia, and hallucinations) are the most common adverse effects reported. Severe toxicity signs compatible with excessive serotonin activity, such as hyperthermia, metabolic acidosis, and prolonged rhabdomyolysis, have also been observed. Reinforcing potential observed in animals predicts a high potential for addiction and abuse in users. In case of overdose, no specific antidote exists and no curative treatment has been approved by health authorities. Therefore, management of acute toxic effects is mainly extrapolated from experience with cocaine/amphetamines.
取代卡西酮是卡西酮的合成类似物,可被视为侧链带有β-酮基团的苯乙胺衍生物。它们于21世纪中期出现在娱乐性毒品市场,如今已成为一大类新型流行滥用药物。最初被视为合法兴奋剂,其法律地位因国家而异且迅速变化,政府机构正推动对其进行管控。一些卡西酮(如二乙丙胺苯丙酮或吡咯戊酮)曾用于医疗环境,安非他酮实际上被用于戒烟。取代卡西酮可从互联网网站、零售店和街头毒贩处广泛获取。它们可以化学名称、引人联想的名称或通用名称出售,这使得它们难以识别。幸运的是,近年来已开发出分析方法来解决这一问题。取代卡西酮以粉末形式存在,可通过鼻吸、口服或静脉注射自行给药。它们通过促使儿茶酚胺(多巴胺、去甲肾上腺素和5-羟色胺)释放并阻断其在中枢和外周神经系统中的再摄取,从而起到中枢神经系统兴奋剂的作用。它们还可能作为非选择性底物或强效阻滞剂降低多巴胺和5-羟色胺转运体功能,并可能抑制单胺氧化酶的作用。然而,不同取代卡西酮在体外的效力存在显著差异。使用者报告的预期效果包括精力增加、情感共鸣增强和性欲改善。心血管方面(心动过速、高血压)以及精神/神经方面的体征/症状(激动、癫痫发作、偏执和幻觉)是报告的最常见不良反应。还观察到与5-羟色胺活动过度相符的严重毒性体征,如高热、代谢性酸中毒和持续性横纹肌溶解。在动物身上观察到的强化潜力预示着使用者有很高的成瘾和滥用可能性。一旦过量,不存在特效解毒剂,且卫生当局未批准任何治疗方法。因此,急性毒性作用的处理主要是根据可卡因/安非他明的经验推断而来。