Sunder Sharma S, Bhargava H N
Department of Pharmaceutics and Pharmacodynamics (M/C 865), The University of Illinois at Chicago, Health Sciences Center, Chicago, Ill., USA.
Pharmacology. 1998 Nov;57(5):229-32. doi: 10.1159/000028246.
The effects of ibogaine, an alkaloid isolated form the bark of the African shrub, Tabernathe iboga, and noribogaine, a metabolite of ibogaine, on morphine antinociception were determined in male Swiss-Webster mice. Mice were rendered tolerant to morphine by implanting them with a pellet containing 25 mg of morphine base for 3 days. Placebo pellet-implanted mice served as controls. The antinociception of morphine (10 mg/kg, s.c.) was determined alone or in combination with an appropriate dose of ibogaine or noribogaine. Tolerance to morphine developed as a result of morphine pellet implantation as evidenced by decreased antinociceptive response to morphine. Both ibogaine and noribogaine dose-dependently enhanced morphine antinociception in morphine-tolerant but not in morphine-naive mice. It is concluded that ibogaine and noribogaine enhance morphine antinociception in morphine-tolerant mice.
在雄性瑞士韦伯斯特小鼠中,测定了从非洲灌木伊博格(Tabernathe iboga)树皮中分离出的生物碱伊波加因,以及伊波加因的代谢产物去甲伊波加因对吗啡镇痛作用的影响。通过给小鼠植入含25毫克吗啡碱的药丸3天,使其对吗啡产生耐受性。植入安慰剂药丸的小鼠作为对照。单独或与适当剂量的伊波加因或去甲伊波加因联合使用,测定吗啡(10毫克/千克,皮下注射)的镇痛作用。吗啡药丸植入导致对吗啡产生耐受性,表现为对吗啡的镇痛反应降低。伊波加因和去甲伊波加因在吗啡耐受小鼠中均呈剂量依赖性增强吗啡镇痛作用,但在未接触过吗啡的小鼠中则无此作用。结论是,伊波加因和去甲伊波加因可增强吗啡耐受小鼠的吗啡镇痛作用。