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合成卡西酮类似物的神经毒理学

Neurotoxicology of Synthetic Cathinone Analogs.

作者信息

Angoa-Pérez Mariana, Anneken John H, Kuhn Donald M

机构信息

Research & Development Service, John D. Dingell VA Medical Center, Detroit, MI, 48201, USA.

Department of Psychiatry and Behavioral Neurosciences, Wayne State University School of Medicine, Detroit, MI, 48201, USA.

出版信息

Curr Top Behav Neurosci. 2017;32:209-230. doi: 10.1007/7854_2016_21.

Abstract

The present review briefly explores the neurotoxic properties of methcathinone, mephedrone, methylone, and methylenedioxypyrovalerone (MDPV), four synthetic cathinones most commonly found in "bath salts." Cathinones are β-keto analogs of the commonly abused amphetamines and display pharmacological effects resembling cocaine and amphetamines, but despite their commonalities in chemical structures, synthetic cathinones possess distinct neuropharmacological profiles and produce unique effects. Among the similarities of synthetic cathinones with their non-keto analogs are their targeting of monoamine systems, the release of neurotransmitters, and their stimulant properties. Most of the literature on synthetic cathinones has focused on describing their properties as psychostimulants, their behavioral effects on locomotion, memory, and potential for abuse, whereas descriptions of their neurotoxic properties are not abundant. The biochemical gauges of neurotoxicity induced by non-keto analogs are well studied in humans and experimental animals and include their ability to induce neuroinflammation, oxidative stress, excitotoxicity, temperature alterations as well as dysregulation of neurotransmitter systems and induce changes in monoamine transporters and receptors. These neurotoxicity gauges will serve as parameters to discuss the effects of the four previously mentioned synthetic cathinones alone or in combination with either another cathinone or with some of their non-keto analogs. Bath salts are not a defined combination of drugs and may consist of one synthetic cathinone compound or combinations of more cathinones. Furthermore, this review also presents some of the mechanisms that are thought to underlie this toxicity. A better understanding of the cellular and molecular mechanisms involved in the synthetic cathinones-induced neurotoxicity should contribute to generate modern therapeutic approaches to prevent or attenuate the adverse consequences of use of these drugs in humans.

摘要

本综述简要探讨了甲卡西酮、甲氧麻黄酮、亚甲二氧甲基苯丙胺和亚甲基二氧吡咯戊酮(MDPV)这四种在“浴盐”中最常见的合成卡西酮的神经毒性特性。卡西酮是常见滥用苯丙胺类药物的β - 酮类似物,具有类似于可卡因和苯丙胺的药理作用,但尽管它们在化学结构上有共性,合成卡西酮具有独特的神经药理学特征并产生独特的效应。合成卡西酮与其非酮类似物的相似之处包括它们对单胺系统的靶向作用、神经递质的释放以及它们的兴奋特性。关于合成卡西酮的大多数文献都集中在描述它们作为精神兴奋剂的特性、它们对运动、记忆的行为影响以及滥用潜力,而对它们神经毒性特性的描述并不丰富。非酮类似物诱导的神经毒性的生化指标在人类和实验动物中已有充分研究,包括它们诱导神经炎症、氧化应激、兴奋性毒性、体温变化以及神经递质系统失调和诱导单胺转运体和受体变化的能力。这些神经毒性指标将作为参数来讨论上述四种合成卡西酮单独使用或与另一种卡西酮或其一些非酮类似物联合使用的效果。浴盐不是一种明确的药物组合,可能由一种合成卡西酮化合物或多种卡西酮的组合组成。此外,本综述还介绍了一些被认为是这种毒性基础的机制。更好地理解合成卡西酮诱导神经毒性所涉及的细胞和分子机制,应该有助于产生现代治疗方法,以预防或减轻人类使用这些药物的不良后果。

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