Szumlinski K K, Balogun M Y, Maisonneuve I M, Glick S D
Center for Neuropharmacology and Neuroscience, Albany Medical College, NY 12208, USA.
Psychopharmacology (Berl). 2000 Aug;151(2-3):234-41. doi: 10.1007/s002130000478.
The phenomenon of sensitization has been theoretically implicated in mediating various aspects of drug addiction. Recent dose-response studies demonstrated that pretreatment with the putative antiaddictive agent, ibogaine (IBO), and a synthetic iboga alkaloid congener, 18-methoxycoronaridine (18-MC), increase the potency of cocaine to elicit behavioral sensitization, an effect proposed to contribute, in part, to their ability to attenuate drug self-administration.
As abuse of the methylated amphetamine derivative, methamphetamine (METH), is a growing public health concern, the present study determined the interactions between IBO and 18-MC and the expression of METH-induced behavioral sensitization.
The effects of pretreatment with 18-MC (40 mg/kg, IP, 19 h earlier) on the expression of METH-induced locomotion (0, 0.25, 0.5, 1 and 2 mg/kg, IP) and the effects of pretreatment with either IBO or 18-MC on the expression of METH-induced stereotypy (2 and 4 mg/kg, IP) were assessed in rats treated chronically with either METH (4 mg/kg daily for 7 days) or saline.
Compared to vehicle-pretreated controls, 18-MC produced an overall enhancement in METH-induced locomotion in rats treated chronically, but not acutely, with METH. In addition, both iboga agents increased the stereotypic response to METH.
Iboga agents augment both the locomotor and stereotypic effects of METH in a manner consistent with previous reports for cocaine. Thus, it appears that iboga agents interact in a similar manner with the neural mechanisms mediating motor hyperactivity induced by the chronic administration of stimulant drugs.
致敏现象在理论上与药物成瘾的各个方面有关。最近的剂量反应研究表明,用假定的抗成瘾剂伊波加因(IBO)和一种合成的伊波加生物碱同系物18-甲氧基柯诺里定(18-MC)进行预处理,会增加可卡因引发行为致敏的效力,这一效应被认为部分有助于它们减弱药物自我给药的能力。
由于甲基苯丙胺衍生物甲基苯丙胺(METH)的滥用日益引起公众健康关注,本研究确定了IBO和18-MC之间的相互作用以及METH诱导的行为致敏的表达。
在长期用METH(4mg/kg,每日一次,共7天)或生理盐水处理的大鼠中,评估用18-MC(40mg/kg,腹腔注射,提前19小时)预处理对METH诱导的运动(0、0.25、0.5、1和2mg/kg,腹腔注射)表达的影响,以及用IBO或18-MC预处理对METH诱导的刻板行为(2和4mg/kg,腹腔注射)表达的影响。
与用赋形剂预处理的对照组相比,18-MC在长期而非急性用METH处理的大鼠中总体上增强了METH诱导的运动。此外,两种伊波加制剂都增加了对METH的刻板反应。
伊波加制剂增强了METH的运动和刻板效应,其方式与先前关于可卡因的报道一致。因此,看来伊波加制剂与介导慢性给予兴奋剂药物所诱导的运动亢进的神经机制以相似的方式相互作用。