Pharmacology and Neuroscience, University of North Texas Health Science Center, Fort Worth, Texas, USA.
Addict Biol. 2021 Jul;26(4):e12987. doi: 10.1111/adb.12987. Epub 2020 Nov 5.
A new generation of novel cathinone compounds has been developed as stimulant substitutes to avoid drug control laws and detection of use by blood tests. Dipentylone, N-ethylhexedrone, 4-chloroethcathinone (4-CEC), and 4'-methyl-α-pyrrolidinohexiophenone (MPHP) were tested for in vivo psychostimulant-like effects to assess their abuse liability. Locomotor activity was assessed in an open-field assay using Swiss-Webster mice to screen for locomotor stimulant effects and to identify behaviorally-active dose ranges, times of peak effect, and durations of action. Discriminative stimulus effects were assessed in separate groups of Sprague-Dawley rats trained to discriminate cocaine or methamphetamine from vehicle. Dipentylone, N-ethylhexedrone, 4-CEC, and MPHP dose-dependently increased locomotor activity. Dipentylone, N-ethylhexedrone, and MPHP produced maximal stimulant effects similar to cocaine and methamphetamine. 4-CEC was less efficacious, producing peak stimulant effects of about 74% of that of methamphetamine. The compounds were less potent than methamphetamine and approximately equipotent with cocaine. The doses of cocaine, methamphetamine, dipentylone, and 4-CEC that produced peak effects lasted 2 to 3 h, the peak dose of N-ethylhexedrone lasted 4 h, and the peak dose of MPHP lasted 6 h. All four compounds fully substituted for the discriminative stimulus effects of methamphetamine and cocaine, although full substitution by 4-CEC occurred at doses that substantially decreased response rate. Only 4-CEC fully substituted for MDMA. These data provide evidence that the novel cathinone compounds dipentylone, N-ethylhexedrone, 4-CEC, and MPHP demonstrate potential for abuse as psychostimulants, given their ability to stimulate locomotor activity and their substitution for the discriminative stimulus effects of methamphetamine and cocaine.
新一代的新型苯丙胺化合物已被开发为兴奋剂替代品,以避免药物管制法和通过血液检测发现使用情况。二戊基酮、N-乙基己基酮、4-氯乙基卡西酮(4-CEC)和 4'-甲基-α-吡咯烷己基苯丙酮(MPHP)被测试了体内拟交感神经样作用,以评估其滥用倾向。使用瑞士-韦伯斯特小鼠在开放场试验中评估运动活动,以筛选运动兴奋剂作用,并确定行为活性剂量范围、峰值效应时间和作用持续时间。在分别接受训练以区分可卡因或甲基苯丙胺与载体的斯普拉格-道利大鼠组中评估了鉴别性刺激作用。二戊基酮、N-乙基己基酮、4-CEC 和 MPHP 剂量依赖性地增加运动活动。二戊基酮、N-乙基己基酮和 MPHP 产生与可卡因和甲基苯丙胺相似的最大兴奋剂作用。4-CEC 的效果较弱,产生的兴奋剂峰值作用约为甲基苯丙胺的 74%。这些化合物的效力低于甲基苯丙胺,与可卡因的效力大致相当。产生峰值效应的可卡因、甲基苯丙胺、二戊基酮和 4-CEC 的剂量持续 2 至 3 小时,N-乙基己基酮的峰值剂量持续 4 小时,MPHP 的峰值剂量持续 6 小时。所有四种化合物都完全替代了甲基苯丙胺和可卡因的鉴别性刺激作用,尽管 4-CEC 完全替代的剂量显著降低了反应率。只有 4-CEC 完全替代了 MDMA。这些数据提供了证据,表明新型苯丙胺化合物二戊基酮、N-乙基己基酮、4-CEC 和 MPHP 具有作为拟交感神经兴奋剂滥用的潜力,因为它们能够刺激运动活动,并替代甲基苯丙胺和可卡因的鉴别性刺激作用。