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Toxicity of amphetamines: an update

机译:安非他命的毒性:最新动态

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Amphetamines represent a class of psychotropic compounds, widely abused for their stimulant, euphoric, anorectic, and, in some cases, emphathogenic, entactogenic, and hallucinogenic properties. These compounds derive from the β-phenylethylamine core structure and are kinetically and dynamically characterized by easily crossing the blood–brain barrier, to resist brain biotransformation and to release monoamine neurotransmitters from nerve endings. Although amphetamines are widely acknowledged as synthetic drugs, of which amphetamine, methamphetamine, and 3,4-methylenedioxymethamphetamine (MDMA, ecstasy) are well-known examples, humans have used natural amphetamines for several millenniums, through the consumption of amphetamines produced in plants, namely cathinone (khat), obtained from the plant Catha edulis and ephedrine, obtained from various plants in the genus Ephedra. More recently, a wave of new amphetamines has emerged in the market, mainly constituted of cathinone derivatives, including mephedrone, methylone, methedrone, and buthylone, among others. Although intoxications by amphetamines continue to be common causes of emergency department and hospital admissions, it is frequent to find the sophism that amphetamine derivatives, namely those appearing more recently, are relatively safe. However, human intoxications by these drugs are increasingly being reported, with similar patterns compared to those previously seen with classical amphetamines. That is not surprising, considering the similar structures and mechanisms of action among the different amphetamines, conferring similar toxicokinetic and toxicological profiles to these compounds. The aim of the present review is to give an insight into the pharmacokinetics, general mechanisms of biological and toxicological actions, and the main target organs for the toxicity of amphetamines. Although there is still scarce knowledge from novel amphetamines to draw mechanistic insights, the long-studied classical amphetamines—amphetamine itself, as well as methamphetamine and MDMA, provide plenty of data that may be useful to predict toxicological outcome to improvident abusers and are for that reason the main focus of this review.
机译:苯丙胺代表一类精神药物,由于其刺激性,欣快性,厌食性,在某些情况下具有促发性,促触觉性和致幻性而被广泛滥用。这些化合物源自β-苯乙胺核心结构,具有动力学和动态特征,可轻松穿越血脑屏障,抵抗脑部生物转化并从神经末梢释放单胺类神经递质。尽管苯丙胺是公认的合成药物,其中苯丙胺,甲基苯丙胺和3,4-亚甲基二氧基甲基苯丙胺(摇头丸)是众所周知的例子,但人类通过食用植物中生产的苯丙胺,将天然苯丙胺用于数千年,即从植物Catha edulis和麻黄碱中获得的卡西酮(khat),从麻黄属中的多种植物中获得。最近,市场上涌现了一波新的苯丙胺类药,主要由卡西酮衍生物组成,包括甲氧麻黄酮,甲酮,甲氧麻黄酮和丁酮等。尽管苯丙胺中毒仍然是急诊科和医院入院的常见原因,但人们经常发现,苯丙胺衍生物(即最近出现的苯丙胺衍生物)相对安全是一种诡秘。但是,越来越多地报道了这些药物引起的人体中毒,其模式与以前使用经典苯丙胺所见的模式相似。考虑到不同的苯丙胺之间具有相似的结构和作用机理,并赋予这些化合物相似的毒代动力学和毒理学特征,这不足为奇。本综述的目的是深入了解苯丙胺的药代动力学,生物学和毒理学作用的一般机制以及主要靶器官。尽管仍然缺乏从新颖的苯丙胺获得的机械学见解的知识,但经过长期研究的经典苯丙胺(苯丙胺本身)以及甲基苯丙胺和MDMA可提供大量数据,这些数据可用于预测对即兴滥用者的毒理学结果,为此原因是本次审查的重点。

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