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化学生物神经科学中的经典毒品:α-吡咯烷戊基苯丙酮(“浴盐”)。

DARK Classics in Chemical Neuroscience: α-Pyrrolidinovalerophenone ("Flakka").

机构信息

Ural Federal University , Ekaterinburg 620002 , Russia.

Institute of Experimental Medicine, Almazov National Medical Research Centre , Ministry of Healthcare of Russian Federation , St. Petersburg 194156 , Russia.

出版信息

ACS Chem Neurosci. 2019 Jan 16;10(1):168-174. doi: 10.1021/acschemneuro.8b00525. Epub 2018 Nov 26.

Abstract

Flakka (alpha-pyrrolidinovalerophenone, α-PVP) is a new psychoactive substance, chemically close to cathinone, the primary psychoactive alkaloid of khat ( Catha edulis). Like other synthetic cathinones, α-PVP is a potent inhibitor of the dopamine and norepinephrine transporters. Its robust clinical effects include hallucinations, arousal, aggression/violence, and euphoria. In animal models, α-PVP evokes hyperlocomotion and aberrant/stereotypic behaviors. Here, we discuss the history, synthesis, pharmacological mechanisms, metabolism, abuse potential, and societal impact of α-PVP. Today, α-PVP is a tightly controlled substance, currently banned in the United States and other countries worldwide. However, the growing abuse and complex central nervous system (CNS) effects of α-PVP remain poorly understood, necessitating further pharmacological and pharmacogenetic studies of this drug. Its interesting pharmacological profile (co-inhibition of dopamine and norepinephrine, but not serotonin, transporters) also calls for further studies of α-PVP in animal models, to dissect serotonergic from other monoaminergic mechanisms of action of drugs of abuse. Finally, screening α-PVP and related compounds in vivo may foster discovery of new CNS drugs, including developing novel CNS drugs and identifying their molecular targets.

摘要

氟烷(α- 吡咯烷酮戊基苯酮,α-PVP)是一种新型精神活性物质,在化学结构上与卡西酮(巧茶的主要精神活性生物碱)相近。与其他合成卡西酮一样,α-PVP 是一种强效的多巴胺和去甲肾上腺素转运体抑制剂。其强烈的临床效应包括幻觉、觉醒、攻击/暴力和欣快。在动物模型中,α-PVP 会引起过度活跃和异常/刻板行为。在这里,我们讨论了 α-PVP 的历史、合成、药理学机制、代谢、滥用潜力和社会影响。如今,α-PVP 是一种受到严格控制的物质,目前在美国和其他国家被禁止使用。然而,α-PVP 的滥用情况日益严重,其对中枢神经系统的复杂影响仍未得到充分了解,因此需要对这种药物进行进一步的药理学和药物遗传学研究。其有趣的药理学特征(同时抑制多巴胺和去甲肾上腺素,而不是 5-羟色胺转运体)也需要在动物模型中进一步研究 α-PVP,以分离出药物滥用的 5-羟色胺能和其他单胺能作用机制。最后,在体内筛选 α-PVP 和相关化合物可能会促进新型中枢神经系统药物的发现,包括开发新型中枢神经系统药物和鉴定其分子靶点。

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