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甲氧麻黄酮和萘黄酮对小鼠的可卡因样辨别刺激效应

Cocaine-Like Discriminative Stimulus Effects of Mephedrone and Naphyrone in Mice.

作者信息

Gannon Brenda M, Fantegrossi William E

机构信息

Department of Pharmacology and Toxicology, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.

出版信息

J Drug Alcohol Res. 2016;5. doi: 10.4303/jdar/236009. Epub 2016 Dec 31.

Abstract

BACKGROUND

In recent years, commercial products containing synthetic cathinone analogues have emerged as illicit drugs of abuse. These cathinones are structurally similar to the psychostimulants 3,4-methylenedioxymethamphetamine (MDMA) and methamphetamine (METH), and produce their effects via interactions with monoamine transporters, where smaller compounds (e.g., mephedrone) are amphetamine-like monoamine releasers, while the structurally larger compounds (e.g., naphyrone) are cocaine-like monoamine reuptake inhibitors. Individual cathinones also differ from one another with respect to selectivity among the three monoamine transporters.

STATEMENT OF PURPOSE OF STUDY

This study was designed to assess the cocaine-like interoceptive effects of synthetic cathinone analogues functioning as passive monoamine reuptake inhibitors (naphyrone) or as releasers (mephedrone) in mice in order to compare effectiveness (degree of substitution) and potency with positive control psychostimulants cocaine, METH, and MDMA.

PROCEDURES

In the present study, mice were trained to discriminate 10 mg/kg cocaine from saline, and substitutions with METH, MDMA, mephedrone, naphyrone, and morphine were performed.

MAIN FINDINGS

Mice reliably discriminated the cocaine training dose from saline, and METH, MDMA, mephedrone, and naphyrone all elicited full cocaine-like responding, while morphine did not. Potency differences were observed such that METH was most potent, while mephedrone, cocaine, MDMA, and naphyrone exhibited roughly equivalent potency.

PRINCIPAL CONCLUSIONS

These data confirm that interaction with DAT is an important component of cocaine-like discriminative stimulus effects, and suggest that synthetic cathinones likely elicit psychostimulant-like abuse-related effects.

摘要

背景

近年来,含有合成卡西酮类似物的商业产品已成为滥用的非法药物。这些卡西酮在结构上与精神兴奋剂3,4-亚甲基二氧甲基苯丙胺(摇头丸)和甲基苯丙胺(冰毒)相似,并通过与单胺转运体相互作用产生效果,其中较小的化合物(如甲氧麻黄酮)是苯丙胺样单胺释放剂,而结构较大的化合物(如萘黄酮)是可卡因样单胺再摄取抑制剂。各个卡西酮在三种单胺转运体之间的选择性方面也彼此不同。

研究目的声明

本研究旨在评估在小鼠中作为被动单胺再摄取抑制剂(萘黄酮)或释放剂(甲氧麻黄酮)发挥作用的合成卡西酮类似物的可卡因样内感受效应,以便与阳性对照精神兴奋剂可卡因、冰毒和摇头丸比较有效性(替代程度)和效力。

实验步骤

在本研究中,训练小鼠区分10毫克/千克可卡因和生理盐水,并进行用冰毒、摇头丸、甲氧麻黄酮、萘黄酮和吗啡的替代实验。

主要发现

小鼠能够可靠地区分可卡因训练剂量和生理盐水,冰毒、摇头丸、甲氧麻黄酮和萘黄酮均引发完全的可卡因样反应,而吗啡则没有。观察到效力差异,使得冰毒效力最强,而甲氧麻黄酮、可卡因、摇头丸和萘黄酮表现出大致相当的效力。

主要结论

这些数据证实与多巴胺转运体(DAT)的相互作用是可卡因样辨别刺激效应的重要组成部分,并表明合成卡西酮可能引发类似精神兴奋剂的与滥用相关的效应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/182e/5393345/2d202efa723d/nihms850763f1.jpg

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