Glick S D, Maisonneuve I M, Dickinson H A
Center for Neuropharmacology and Neuroscience, Albany Medical College, NY 12208, USA.
Neuroreport. 2000 Jun 26;11(9):2013-5. doi: 10.1097/00001756-200006260-00041.
In previous studies, 18-methoxycoronaridine (18-MC), a novel iboga alkaloid congener, has been found to decrease the intravenous self-administration of morphine and cocaine in rats. In the present study, 18-MC (1-40 mg/kg, i.p.) dose-dependently decreased the i.v. self-administration of methamphetamine and nicotine. As in the previous studies, drug self-administration was reduced for > or = 24 h after the highest dose of 18-MC. A comparison of 18-MC's interactions with all four drugs of abuse studied so far indicated that 18-MC is least effective in decreasing methamphetamine self-administration and most potent in decreasing nicotine self-administration. The results suggest that a nicotinic antagonist action of 18-MC contributes to its putative anti-addictive efficacy.
在先前的研究中,已发现一种新型伊博格生物碱同系物18-甲氧基冠狗牙花定碱(18-MC)可减少大鼠静脉注射吗啡和可卡因的自我给药行为。在本研究中,18-MC(1-40毫克/千克,腹腔注射)剂量依赖性地减少了甲基苯丙胺和尼古丁的静脉自我给药。与先前的研究一样,在给予最高剂量的18-MC后,药物自我给药行为减少了≥24小时。对18-MC与目前研究的所有四种滥用药物相互作用的比较表明,18-MC在减少甲基苯丙胺自我给药方面效果最差,而在减少尼古丁自我给药方面效果最强。结果表明,18-MC的烟碱拮抗剂作用有助于其假定的抗成瘾功效。