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设计师药物2.0

Designer Drugs 2.0.

作者信息

Huestis M A, Tyndale R F

机构信息

Chemistry and Drug Metabolism, IRP, National Institute on Drug Abuse, National Institutes of Health, Baltimore, Maryland, USA.

University of Maryland School of Medicine, Baltimore, Maryland, USA.

出版信息

Clin Pharmacol Ther. 2017 Feb;101(2):152-157. doi: 10.1002/cpt.575.

Abstract

This "Designer Drugs 2.0" issue of Clinical Pharmacology & Therapeutics focuses on novel psychoactive substances, primarily cannabinoids and cathinones, and the repurposing of established psychoactive compounds (e.g., modafinil, psilocybin, lysergic acid diethylamide, and 3,4-methylenedioxymethamphetamine) that simultaneously offer new pharmacotherapies and pose serious health problems. Novel psychoactive substances were initially used as potent tools to investigate endogenous neurotransmitter systems; for example, synthetic cannabinoids have much higher potency than Δ9-tetrahydrocannabinol at the cannabinoid receptors. However, they are now being used illicitly as well as being tested for their efficacy in numerous clinical indications. Likewise, previously established psychoactive drugs are being repurposed as treatments for a wide variety of indications where currently approved medications are ineffective. This set of papers examines the arising problems associated with designer drugs (e.g., adverse events, psychosis, rapid new synthesis, abuse liability testing, internet sales, scheduling) as well as the potential therapeutic promises in areas as diverse as cognition enhancement, exercise-mimetics, epilepsy, multiple sclerosis, and posttraumatic stress disorder.

摘要

本期《临床药理学与治疗学》的“设计药物2.0”专刊聚焦于新型精神活性物质,主要是大麻素和卡西酮,以及现有精神活性化合物(如莫达非尼、裸盖菇素、麦角酸二乙胺和3,4-亚甲基二氧甲基苯丙胺)的重新利用,这些物质在提供新的药物治疗方法的同时,也带来了严重的健康问题。新型精神活性物质最初被用作研究内源性神经递质系统的有力工具;例如,合成大麻素在大麻素受体上的效力比Δ9-四氢大麻酚高得多。然而,它们现在正被非法使用,并且正在针对多种临床适应症测试其疗效。同样,以前已有的精神活性药物正在被重新用作治疗目前批准药物无效的多种适应症的药物。这组论文探讨了与设计药物相关的新出现问题(如不良事件、精神病、快速新合成、滥用可能性测试、网络销售、管制安排),以及在认知增强、运动模拟、癫痫、多发性硬化症和创伤后应激障碍等不同领域的潜在治疗前景。

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