三种色胺:α -甲基色胺、5-甲氧基- α -甲基色胺和5-甲氧基- n, n -二异丙基色胺对小鼠急性毒性、运动活性和致幻行为的影响。

IF 1.6 4区 心理学 Q3 BEHAVIORAL SCIENCES
Kaixi Li, Nan Li, Yuanyuan Chen, Xiangyu Li, Yanling Qiao, Dan Wang, Bin Di, Peng Xu
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引用次数: 0

摘要

α -甲基色胺(AMT)、5-甲氧基- α -甲基色胺(5-MeO-AMT)和5-甲氧基- n, n -二异丙基色胺(5-MeO-DiPT)是具有致幻剂性质的合成色胺,在世界范围内被广泛滥用。然而,关于其药理特性的研究和可用数据一直很缺乏。本研究的目的是探讨AMT和5-MeO-DiPT的安全性,比较相同条件下AMT、5-MeO-AMT和5-MeO-DiPT在运动表现和致幻样行为方面的影响,以及5-羟色胺- 2a受体拮抗剂(M100907)对致幻样行为的作用。结果表明,AMT和5-MeO-DiPT均表现出一定的急性毒性作用。AMT、5-MeO-AMT和5-MeO-DiPT抑制小鼠的运动活动并诱导头抽搐反应(HTR)。预处理M100907 (0.01 mg/kg)可阻断小鼠AMT、5-MeO-AMT和5-MeO-DiPT诱导的HTR。本研究结果表明,这三种色胺是有毒的,抑制运动活动,并有致幻作用。这些结果提供了实验数据,可以为未来的控制策略和对这些物质的深入机理研究提供基础支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of three tryptamines: alpha-methyltryptamine, 5-methoxy-alpha-methyltryptamine, and 5-methoxy-N,N-diisopropyltryptamine on acute toxicity, locomotor activity, and hallucinogenic behavior in mice.

Alpha-methyltryptamine (AMT), 5-methoxy-alpha-methyltryptamine (5-MeO-AMT), and 5-methoxy-N,N-diisopropyltryptamine (5-MeO-DiPT) are synthetic tryptamines with hallucinogenic-like properties that are widely abused worldwide. There, however, has been a paucity of research and a lack of available data on their pharmacological properties. The objective of this study was to investigate the safety of AMT and 5-MeO-DiPT and to compare the effects of AMT, 5-MeO-AMT, and 5-MeO-DiPT under identical conditions in terms of locomotor performance and hallucinogenic-like behavior, and the role of 5-hydroxytryptamine-2A receptor antagonists (M100907) on hallucinogenic-like behavior. The results showed that both AMT and 5-MeO-DiPT exhibited some acute toxic effects. AMT, 5-MeO-AMT, and 5-MeO-DiPT inhibited locomotor activity and induced head-twitch response (HTR) in mice. Pretreatment with M100907 (0.01 mg/kg) blocked AMT, 5-MeO-AMT, and 5-MeO-DiPT induced HTR in mice. The findings of this study demonstrated that the three tryptamines are toxic, inhibit locomotor activity, and have hallucinogenic effects. These results provide experimental data that can provide fundamental support for future control strategies and in-depth mechanistic studies of these substances.

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来源期刊
Behavioural Pharmacology
Behavioural Pharmacology 医学-行为科学
CiteScore
3.40
自引率
0.00%
发文量
84
审稿时长
6-12 weeks
期刊介绍: Behavioural Pharmacology accepts original full and short research reports in diverse areas ranging from ethopharmacology to the pharmacology of schedule-controlled operant behaviour, provided that their primary focus is behavioural. Suitable topics include drug, chemical and hormonal effects on behaviour, the neurochemical mechanisms under-lying behaviour, and behavioural methods for the study of drug action. Both animal and human studies are welcome; however, studies reporting neurochemical data should have a predominantly behavioural focus, and human studies should not consist exclusively of clinical trials or case reports. Preference is given to studies that demonstrate and develop the potential of behavioural methods, and to papers reporting findings of direct relevance to clinical problems. Papers making a significant theoretical contribution are particularly welcome and, where possible and merited, space is made available for authors to explore fully the theoretical implications of their findings. Reviews of an area of the literature or at an appropriate stage in the development of an author’s own work are welcome. Commentaries in areas of current interest are also considered for publication, as are Reviews and Commentaries in areas outside behavioural pharmacology, but of importance and interest to behavioural pharmacologists. Behavioural Pharmacology publishes frequent Special Issues on current hot topics. The editors welcome correspondence about whether a paper in preparation might be suitable for inclusion in a Special Issue.
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