18-MC reduces methamphetamine and nicotine self-administration in rats

18-MC reduces methamphetamine and nicotine self-administration in rats
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DOI:
10.1097/00001756-200006260-00041
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发表时间:
2000-06-26
期刊:
影响因子:
1.7
通讯作者:
Dickinson, HA
Dickinson, HA
中科院分区:
医学4区
文献类型:
--
作者:
Glick, SD;Maisonneuve, IM;Dickinson, HA

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在以前的研究中,发现18-甲氧基冠孢定(18-MC),一种新的iboga生物碱同系物,减少吗啡和可卡因在大鼠静脉自给药。在本研究中,18-MC(1-40 mg/kg,i. p.)剂量依赖性地减少了甲基苯丙胺和尼古丁的静脉内自我给药。与之前的研究一样,在18-MC最高剂量给药后24 h以上,药物自我给药减少。18-MC与迄今为止研究的所有四种滥用药物的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,在减少尼古丁自我给药方面效果最强。结果表明,烟碱拮抗作用的18-MC有助于其推定的抗成瘾疗效。NeuroReport 11:2013-2015(C)2000 Lippincott威廉姆斯& Wilkins.
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 greater than or equal to 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. NeuroReport 11:2013-2015 (C) 2000 Lippincott Williams & Wilkins.