内毒素潜在毒性的估计-电脑研究

Milena Jadrijević-Mladar Takač, Tin Takač
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引用次数: 0

摘要

摇头丸(MDMA)及其结构类似物能够诱导“致幻综合征”,这是一种可逆的、可控的人类意识改变,其特征是情绪放松、幸福感和同理心。这使得MDMA成为最受欢迎的娱乐性药物,滥用的可能性很大。最近有越来越多的证据表明,MDMA可用于MDMA辅助心理治疗,以治疗创伤后应激障碍(PTSD)、自闭症焦虑、酗酒和情绪障碍。青少年和年轻人普遍认为摇头丸是一种安全的药物。然而,通常以这个名字出售的“街头毒品”在纯度上差别很大,而且经常含有掺假物或未申报的、性质不明的致假原。(1 - 4)研究了Entactogens(图1)和参比分子,抗抑郁药paroxetine (SSRI)和venflaxine (SNRI)的毒性潜力和通过膜转运体对药物-药物相互作用(DDI)的亲和力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Estimating the Toxic Potential of Entactogens – In silico Study
Ecstasy (MDMA) and its structural analogs are capable of inducing an ”entactogenic syndrome”, a reversible controlled alteration of consciousness in humans characterized by emotional relaxation, feelings of happiness, and empathy. This makes MDMA the most popular recreational drug with a high potential for abuse. Recently there has been increasing evidence that MDMA may be used in MDMA-assisted psychotherapy to treat post-traumatic stress disorder (PTSD), autism anxiety, alcoholism, and mood disorders. There is a widespread belief among adolescents and younger adults that ecstasy is a safe drug. However, the “street drugs” that are very commonly sold under this name can vary widely in purity and often contain adulterants or undeclared entactogens with unknown properties. (1‒4) Entactogens (Figure 1) and reference molecules, the antidepressants paroxetine (SSRI) and venflaxine (SNRI), were studied for their toxic potential and affinity for drug-drug interactions (DDI) via membrane transporters.
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