Felszeghy Klara, Espinosa José Manuel, Scarna Hélène, Bérod Anne, Rostène William, Pélaprat Didier
INSERM, U 339, Hôpital Saint-Antoine, Paris Cedex, France.
Neuropsychopharmacology. 2007 Dec;32(12):2601-10. doi: 10.1038/sj.npp.1301382. Epub 2007 Mar 14.
Chronic use of psychostimulants induces enduringly increased responsiveness to a subsequent psychostimulant injection and sensitivity to drug-associated cues, contributing to drug craving and relapse. Neurotensin (NT), a neuropeptide functionally linked to dopaminergic neurons, was suggested to participate in these phenomena. We and others have reported that SR 48692, an NT receptor antagonist, given in pre- or co-treatments with cocaine or amphetamine, alters some behavioral effects of these drugs in rats. However, its efficacy when applied following repeated cocaine administration remains unknown. We, therefore, evaluated the ability of SR 48692, administered after a cocaine regimen, to interfere with the expression of locomotor sensitization and conditioned place preference (CPP) in rats. We demonstrated that the expression of locomotor sensitization, induced by four cocaine injections (15 mg/kg, i.p.) every other day and a cocaine challenge 1 week later, was attenuated by a subsequent 2-week daily administration of SR 48692 (1 mg/kg, i.p.). Furthermore, the expression of cocaine-induced CPP was suppressed by a 10-day SR 48692 treatment started after the conditioning period (four 15 mg/kg cocaine injections every other day). Taken together, our data show that a chronic SR 48692 treatment given after a cocaine regimen partly reverses the expression of locomotor sensitization and CPP in the rat, suggesting that NT participates in the maintenance of these behaviors. Our results support the hypothesis that targeting neuromodulatory systems, such as the NT systems may offer new strategies in the treatment of drug addiction.
长期使用精神兴奋剂会导致对随后注射的精神兴奋剂的反应性持续增加以及对与药物相关线索的敏感性增加,从而导致药物渴望和复发。神经降压素(NT)是一种与多巴胺能神经元功能相关的神经肽,被认为参与了这些现象。我们和其他人曾报道,NT受体拮抗剂SR 48692在与可卡因或苯丙胺进行预处理或联合治疗时,会改变这些药物在大鼠中的一些行为效应。然而,在反复给予可卡因后应用时其疗效仍不清楚。因此,我们评估了在可卡因给药方案后给予SR 48692以干扰大鼠运动敏化和条件性位置偏爱(CPP)表达的能力。我们证明,每隔一天注射四次可卡因(15毫克/千克,腹腔注射)并在1周后进行可卡因激发所诱导的运动敏化表达,在随后每天给予SR 48692(1毫克/千克,腹腔注射)2周后减弱。此外,在条件化期(每隔一天注射四次15毫克/千克可卡因)后开始的为期10天的SR 48692治疗抑制了可卡因诱导的CPP的表达。综上所述,我们的数据表明,在可卡因给药方案后给予慢性SR 48692治疗可部分逆转大鼠运动敏化和CPP的表达,提示NT参与了这些行为的维持。我们的结果支持这样的假说,即靶向神经调节系统,如NT系统,可能为药物成瘾的治疗提供新策略。