Prinssen E P, Kleven M S, Vignon J, Kamenka J M, Koek W
Centre de Reserche Pierre Fabre, Castres, France.
J Pharmacol Exp Ther. 1996 Mar;276(3):904-11.
The present study investigated the effects of repeated administration of the dopamine reuptake inhibitors N-[1-(2-benzo(b)thiophenyl)cyclohexyl]piperidine (BTCP) and cocaine on locomotor activity, as well as their ability to induce or express cross-sensitization. Male mice were injected with a fixed dose of BTCP or cocaine (10,20 or 40 mg/kg i.p.) for 3 consecutive days and challenged on the 4th day with one of several doses of BTCP and/or cocaine. After every daily treatment, locomotor activity was assessed. Repeated administration of cocaine produced sensitization to the locomotor activity produced by different challenge doses of both cocaine (2.5-56.6 mg/kg i.p.) and BTCP (2.5-80 mg/kg, i.p.) on day 4. Repeated administration of low and intermediate doses of BTCP did not significantly affect the locomotor activity produced by different challenge doses of BTCP, whereas tolerance-like effects were observed after the higher dose, 40 mg/kg, particularly during the 3-day regimen. Repeated administration of BTCP dose-dependently produced leftward and downward shifts of the cocaine dose-response curve. The results indicate that, under identical treatment conditions, cocaine and BTCP differ markedly with respect to their ability to cause sensitization, but differ less in terms of their ability to elicit locomotor activity in sensitized animals. The demonstration of cross-sensitization between BTCP and cocaine provides evidence for a shared mechanism of action; however, the present results also suggest that the chronic effects of cocaine and BTCP are not identical.
本研究调查了重复给予多巴胺再摄取抑制剂N-[1-(2-苯并噻吩基)环己基]哌啶(BTCP)和可卡因对运动活性的影响,以及它们诱导或表达交叉致敏的能力。雄性小鼠连续3天注射固定剂量的BTCP或可卡因(10、20或40mg/kg腹腔注射),并在第4天用几种剂量的BTCP和/或可卡因之一进行激发。每天治疗后,评估运动活性。重复给予可卡因使小鼠对第4天不同激发剂量的可卡因(2.5-56.6mg/kg腹腔注射)和BTCP(2.5-80mg/kg腹腔注射)所产生的运动活性产生致敏。重复给予低剂量和中等剂量的BTCP对不同激发剂量的BTCP所产生的运动活性没有显著影响,而在较高剂量40mg/kg时观察到类似耐受的效应,尤其是在3天给药方案期间。重复给予BTCP剂量依赖性地使可卡因剂量-反应曲线向左和向下移动。结果表明,在相同的治疗条件下,可卡因和BTCP在引起致敏的能力方面有显著差异,但在致敏动物中引发运动活性的能力方面差异较小。BTCP和可卡因之间交叉致敏的证明为共同的作用机制提供了证据;然而,目前的结果也表明可卡因和BTCP的慢性效应并不相同。