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通过实验动物模型了解致幻性兴奋药物对中枢神经系统的影响。

Understanding Central Nervous System Effects of Deliriant Hallucinogenic Drugs through Experimental Animal Models.

机构信息

Institute of Translational Biomedicine, St. Petersburg State University , St. Petersburg 199034 , Russia.

Almazov National Medical Research Centre , St. Petersburg 197341 , Russia.

出版信息

ACS Chem Neurosci. 2019 Jan 16;10(1):143-154. doi: 10.1021/acschemneuro.8b00433. Epub 2018 Oct 16.

Abstract

Hallucinogenic drugs potently alter human behavior and have a millennia-long history of use for medicinal and religious purposes. Interest is rapidly growing in their potential as CNS modulators and therapeutic agents for brain conditions. Antimuscarinic cholinergic drugs, such as atropine and scopolamine, induce characteristic hyperactivity and dream-like hallucinations and form a separate group of hallucinogens known as "deliriants". Although atropine and scopolamine are relatively well-studied drugs in cholinergic physiology, deliriants represent the least-studied class of hallucinogens in terms of their behavioral and neurological phenotypes. As such, novel approaches and new model organisms are needed to investigate the CNS effects of these compounds. Here, we comprehensively evaluate the preclinical effects of deliriant hallucinogens in various animal models, their mechanisms of action, and potential interplay with other signaling pathways. We also parallel experimental and clinical findings on deliriant agents and outline future directions of translational research in this field.

摘要

致幻药物能显著改变人类的行为,它们在医学和宗教领域被使用已有数千年的历史。人们对它们作为中枢神经系统调节剂和治疗大脑疾病的治疗药物的潜力越来越感兴趣。拟副交感神经胆碱能药物,如阿托品和东莨菪碱,会引起特征性的多动和梦境般的幻觉,并形成一个被称为“致幻剂”的单独致幻剂类别。尽管阿托品和东莨菪碱在胆碱能生理学方面是研究得比较透彻的药物,但就其行为和神经表型而言,致幻剂是研究最少的致幻剂类别。因此,需要新的方法和新的模式生物来研究这些化合物对中枢神经系统的影响。在这里,我们全面评估了致幻剂在各种动物模型中的临床前作用、它们的作用机制以及它们与其他信号通路的潜在相互作用。我们还将致幻剂的实验和临床发现进行了对比,并概述了该领域转化研究的未来方向。

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