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An In Vitro Study of the Neurotoxic Effects of N-Benzylpiperazine: A Designer Drug of Abuse

机译:N-苄基哌嗪的神经毒性作用的体外研究:一种滥用药物

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摘要

Recently, the number of new psychoactive substances has significantly increased. Despite the systematic introduction of prohibition in trade of medicinal products which mimic the effects of illegal drugs, the problem concerning this group of drugs is still important although knowledge about the mechanism of action of those types of substances is scarce. This study aimed to follow the neurotoxic effect of N-benzylpiperazine (BZP), the central nervous system psychostimulant, using the human cancer LN-18 cell model. The statistically significant elevation of LDH levels, increased mitochondrial membrane potential, decreased ATP and increased ROS production, increased levels of DNA damage marker (8-OHdG) and activation of caspases: -3 and -9 confirmed by Real-Time PCR imply the activation of mitochondrial proapoptotic pathways induced by BZP after 24 h incubation. This study is a novel, preliminary attempt to explain the toxicity of one of the most popular designer drug of abuse at the cellular level.
机译:最近,新的精神活性物质的数量已大大增加。尽管系统地在模仿非法药物影响的药品贸易中实行了禁止措施,但是尽管对这类药物的作用机理的了解很少,但与这类药物有关的问题仍然很重要。这项研究旨在使用人类癌症LN-18细胞模型追踪中枢神经系统精神刺激剂N-苄基哌嗪(BZP)的神经毒性作用。统计学上显着的LDH水平升高,线粒体膜电位增加,ATP降低和ROS产生增加,DNA损伤标记物(8-OHdG)水平升高以及胱天蛋白酶的激活:实时PCR证实了-3和-9暗示激活孵育24小时后BZP诱导的线粒体促凋亡途径的变化这项研究是一种新颖的初步尝试,旨在在细胞水平上解释最流行的设计滥用药物之一的毒性。

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