Eckler J R, Doat M M, Rabin R A, Winter J C
Department of Pharmacology and Toxicology, School of Medicine and Biomedical Sciences, University at Buffalo, 102 Farber Hall, Buffalo, NY 14214-3000, USA.
Life Sci. 2002 Aug 2;71(11):1341-7. doi: 10.1016/s0024-3205(02)01861-1.
The present investigation examined the interaction between 2,5-dimethoxy-4-methylamphetamine [DOM] and the selective serotonin reuptake inhibitor [SSRI] citalopram in rats trained with DOM [0.6 mg/kg; 75 min pretreatment time] as a discriminative stimulus. Pretreatment with citalopram at a dose of 1.0 mg/kg shifted the DOM dose response relationship to the left. Unlike previously tested SSRI's, the enhancement of DOM-induced stimulus control occurred in the absence of significant partial substitution by citalopram. DOM brain levels were measured using a GC-MS method both in the presence and absence of citalopram and fluoxetine in order to evaluate the pharmacokinetic contribution to the observed behavioral effect. The data indicated that fluoxetine but not citalopram significantly increased DOM brain levels. It is concluded that the effects of DOM as a discriminative stimulus are potentiated by the acute administration of citalopram and this effect is not mediated by additivity or pharmacokinetic mechanisms.
本研究考察了2,5-二甲氧基-4-甲基苯丙胺[DOM]与选择性5-羟色胺再摄取抑制剂[SSRI]西酞普兰在以DOM[0.6mg/kg;预处理时间75分钟]作为辨别刺激进行训练的大鼠中的相互作用。以1.0mg/kg的剂量预处理西酞普兰可使DOM剂量反应关系向左移动。与之前测试的SSRI不同,西酞普兰在未产生明显部分替代作用的情况下增强了DOM诱导的刺激控制。为了评估药代动力学对观察到的行为效应的影响,在有和没有西酞普兰及氟西汀的情况下,使用气相色谱-质谱法测量DOM的脑内水平。数据表明,氟西汀而非西酞普兰可显著提高DOM的脑内水平。研究得出结论,急性给予西酞普兰可增强DOM作为辨别刺激的效应,且这种效应并非由相加作用或药代动力学机制介导。