Gatch Michael B, Dolan Sean B, Forster Michael J
Department of Pharmacology & Neuroscience, University of North Texas Health Science Center, Fort Worth, Texas, USA.
Behav Pharmacol. 2016 Sep;27(6):497-505. doi: 10.1097/FBP.0000000000000237.
5,6-Methylenedioxy-2-aminoindane (MDAI) has become a common substitute for (±)-3,4-methylenedioxymethamphetamine (MDMA) in Ecstasy. MDAI is known to produce MDMA-like discriminative stimulus effects, but it is not known whether MDAI has psychostimulant or hallucinogen-like effects. MDAI was tested for locomotor stimulant effects in mice and subsequently for discriminative stimulus effects in rats trained to discriminate cocaine (10 mg/kg, intraperitoneally), methamphetamine (1 mg/kg, intraperitoneally), ±MDMA (1.5 mg/kg, intraperitoneally), or (-)-2,5-dimethoxy-4-methylamphetamine hydrochloride (0.5 mg/kg, intraperitoneally) from saline. The ability of MDAI to produce conditioned place preference was also tested in mice. MDAI (3 to 30 mg/kg) depressed locomotor activity from 10 to 60 min. A rebound stimulant effect was observed at 1 to 3.5 h following 30 mg/kg. Lethality occurred in 8/8 mice following 100 mg/kg MDAI. Similarly, MDMA depressed locomotor activity immediately following the administration of 0.25 mg/kg and stimulant effects were observed 50-70 min following the administration of 0.5 and 1 mg/kg. MDAI fully substituted for the discriminative stimulus effects of MDMA (2.5 mg/kg), (-)-2,5-dimethoxy-4-methylamphetamine hydrochloride (5 mg/kg), and cocaine (7.5 mg/kg), but produced only 73% methamphetamine-appropriate responding at a dose that suppressed responding (7.5 mg/kg). MDAI produced tremors at 10 mg/kg in one methamphetamine-trained rat. MDAI produced conditioned place preference from 0.3 to 10 mg/kg. The effects of MDAI on locomotor activity and drug discrimination were similar to those produced by MDMA, having both psychostimulant-like and hallucinogen-like effects; thus, MDAI may have similar abuse potential as MDMA.
5,6-亚甲基二氧基-2-氨基茚满(MDAI)已成为摇头丸中(±)-3,4-亚甲基二氧基甲基苯丙胺(MDMA)的常见替代品。已知MDAI会产生类似MDMA的辨别性刺激效应,但尚不清楚MDAI是否具有精神兴奋剂或致幻剂样效应。对MDAI进行了小鼠运动刺激效应测试,随后对训练用于区分可卡因(10毫克/千克,腹腔注射)、甲基苯丙胺(1毫克/千克,腹腔注射)、±MDMA(1.5毫克/千克,腹腔注射)或盐酸(-)-2,5-二甲氧基-4-甲基苯丙胺(0.5毫克/千克,腹腔注射)与生理盐水的大鼠进行了辨别性刺激效应测试。还在小鼠中测试了MDAI产生条件性位置偏好的能力。MDAI(3至30毫克/千克)在10至60分钟内降低了运动活性。在30毫克/千克后1至3.5小时观察到反弹刺激效应。100毫克/千克MDAI后8只小鼠中有8只死亡。同样,MDMA在给予0.25毫克/千克后立即降低运动活性,在给予0.5和1毫克/千克后50至70分钟观察到刺激效应。MDAI完全替代了MDMA(2.5毫克/千克)、盐酸(-)-2,5-二甲氧基-4-甲基苯丙胺(5毫克/千克)和可卡因(7.5毫克/千克)的辨别性刺激效应,但在抑制反应的剂量(7.5毫克/千克)下仅产生73%的甲基苯丙胺适当反应。MDAI在一只经甲基苯丙胺训练的大鼠中以10毫克/千克产生震颤。MDAI在0.3至10毫克/千克产生条件性位置偏好。MDAI对运动活性和药物辨别的影响与MDMA产生的影响相似,具有精神兴奋剂样和致幻剂样效应;因此,MDAI可能具有与MDMA相似的滥用潜力。