迷幻药2.0

Russell Crandall
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引用次数: 0

摘要

本章的重点是迷幻药作为2010年代中期毒品战争的另一个新兴前线,大多数迷幻物质,如LSD,美斯卡灵和裸盖菇素,自1970年以来被列为附表一。它解释了日程安排如何通过严格的安全要求,FDA的批准,以及为从事药物研究的机构支付昂贵的DEA许可费,给致幻物质及其效果的科学研究造成了重大障碍。它还叙述了1989年FDA建立的试点药物评估人员,这使得科学界更容易与政府联系。这一章提到了理查德·斯特拉斯曼(Richard Strassman)博士,他成功地制定了一项涉及DMT和裸盖菇素的研究方案。书中详细描述了斯特拉斯曼是如何为自己的研究辩护的,他认为致幻剂会引发多方面的临床综合症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Psychedelics 2.0
This chapter focuses on psychedelics as another emerging front in the war over the war on drugs in the mid 2010s, with most psychedelic substances, such as LSD, mescaline, and psilocybin, being Schedule I listed since 1970. It explains how the scheduling imposed significant barriers to scientific research on hallucinogenic substances and their effects, through stringent security requirements, FDA approval, and expensive DEA licensing fees for institutions working with the drugs. It also recounts the creation of the Pilot Drug Evaluation Staff by the FDA in 1989, which made it easier for the scientific community to liaise with the administration. The chapter refers to Dr. Richard Strassman, who managed to get a research protocol involving DMT and psilocybin off the ground. It details how Strassman defended his work by arguing that hallucinogens elicit a multifaceted clinical syndrome.
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