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新精神活性物质致命毒性指数。

An index of fatal toxicity for new psychoactive substances.

机构信息

1 (Retired), Basingstoke, UK.

2 Psychopharmacology, Drug Misuse & Novel Psychoactive Substances Research Unit, Department of Pharmacy, Pharmacology & Post-graduate Medicine, University of Hertfordshire, Hatfield, UK.

出版信息

J Psychopharmacol. 2018 Jul;32(7):793-801. doi: 10.1177/0269881118754709. Epub 2018 Feb 27.

Abstract

An index of fatal toxicity for new psychoactive substances has been developed based solely on information provided on death certificates. An updated index of fatal toxicity (T), as first described in 2010, was calculated based on the ratio of deaths to prevalence and seizures for the original five substances (amphetamine, cannabis, cocaine/crack, heroin and 3,4-methylenedioxymethylamphetamine). These correlated well with the 2010 index. Deaths were then examined for cases both where the substance was and was not found in association with other substances. This ratio (sole to all mentions; S/A) was then calculated for deaths in the period 1993 to 2016. This new measure of fatal toxicity, expressed by S/A, was well-correlated with the index L (T) of the original reference compounds. The calculation of S/A was then extended to a group of new psychoactive substances where insufficient prevalence or seizure data were available to directly determine a value of T by interpolation of a graph of T versus S/A. Benzodiazepine analogues had particularly low values of S/A and hence T. By contrast, γ-hydroxybutyrate/γ-butyrolactone, α-methyltryptamine, synthetic cannabinoid receptor agonists and benzofurans had a higher fatal toxicity.

摘要

已根据死亡证明中提供的信息,开发出一种新精神活性物质致命毒性指数。根据最初的五种物质(苯丙胺、大麻、可卡因/快克、海洛因和 3,4-亚甲二氧基甲基苯丙胺)的死亡人数与流行率和缉获率之比,计算出了更新的致命毒性指数(T)。这些与 2010 年的指数相关性良好。然后,对有和没有与其他物质一起发现的物质相关的案例进行了死亡检查。然后,针对 1993 年至 2016 年期间的死亡案例计算了这一比例(与所有提及的物质相比;S/A)。通过 S/A 表示的这种新的致命毒性衡量标准与原始参考化合物的指数 L(T)很好地相关。然后,将 S/A 的计算扩展到一组新的精神活性物质,对于这些物质,由于缺乏足够的流行率或缉获数据,无法通过 T 与 S/A 图的内插来直接确定 T 的值。苯并二氮杂䓬类似物的 S/A 值特别低,因此 T 值也很低。相比之下,γ-羟基丁酸/γ-丁内酯、α-甲基色胺、合成大麻素受体激动剂和苯并呋喃具有更高的致命毒性。

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