Meririnne E, Kankaanpää A, Seppälä T
National Public Health Institute, Department of Mental Health and Alcohol Research, Drug Research Unit, Helsinki, Finland.
J Pharmacol Exp Ther. 2001 Aug;298(2):539-50.
In drug addiction, a sensitization phenomenon has been postulated to play a critical role. The aim of our study was to evaluate whether sensitization occurs to the rewarding properties of methylphenidate, a psychostimulant drug known to possess abuse potential, as assessed with the biased conditioned place preference method in rats. In addition, since the brain dopaminergic system is considered to be important in drug-reward, the involvement of dopamine D1- and D2-receptors both in the rewarding properties of methylphenidate and in sensitization to these properties was assessed. Conditioning with methylphenidate at doses of 1.25 to 20 mg/kg increased preference for the paired environment, whereas a dose of 0.31 mg/kg was ineffective. However, following the 7-day sensitization treatment with methylphenidate (0.62-20 mg/kg), conditioning with a dose of 0.31 mg/kg resulted in an increased preference for the paired environment, i.e., the rewarding properties of methylphenidate appeared to be sensitized. Control experiments indicated that the enhancement of preference was not due to attenuation of sensitization treatment-induced withdrawal nor to tolerance to aversive properties of methylphenidate. When conditioned with methylphenidate, D1-antagonist SCH 23390 but not D2-antagonist raclopride prevented place preference. However, when coadministered with methylphenidate during the sensitization treatment, both SCH 23390 and raclopride prevented the development of sensitization. These data indicate that the rewarding properties of methylphenidate are sensitized by prior exposure to the drug and that both D1- and D2-receptors, the latter of which possibly more specifically, appear to be involved in the development of this sensitization.
在药物成瘾中,一种敏感化现象被认为起着关键作用。我们研究的目的是评估是否会对哌甲酯的奖赏特性产生敏感化,哌甲酯是一种已知具有滥用潜力的精神刺激药物,通过大鼠偏倚条件性位置偏爱方法进行评估。此外,由于脑多巴胺能系统被认为在药物奖赏中很重要,因此评估了多巴胺D1和D2受体在哌甲酯奖赏特性及其对这些特性的敏感化中的作用。用1.25至20mg/kg剂量的哌甲酯进行条件化增加了对配对环境的偏爱,而0.31mg/kg的剂量则无效。然而,在用哌甲酯(0.62 - 20mg/kg)进行7天的敏感化处理后,用0.31mg/kg剂量进行条件化导致对配对环境的偏爱增加,即哌甲酯的奖赏特性似乎被敏感化了。对照实验表明,偏爱增强并非由于敏感化处理诱导的戒断减弱,也不是由于对哌甲酯厌恶特性的耐受性。当用哌甲酯进行条件化时,D1拮抗剂SCH 23390可阻止位置偏爱,但D2拮抗剂雷氯必利则不能。然而,在敏感化处理期间与哌甲酯共同给药时,SCH 23390和雷氯必利都可阻止敏感化的发展。这些数据表明,哌甲酯的奖赏特性通过先前接触该药物而被敏感化,并且D1和D2受体似乎都参与了这种敏感化的发展,其中后者可能更具特异性。