Nencini P, Woolverton W L
Department of Psychiatry, Pritzker School of Medicine, University of Chicago, IL 60637.
Psychopharmacology (Berl). 1988;96(1):40-4. doi: 10.1007/BF02431531.
The discriminative stimulus (DS) properties of d-amphetamine (AMP) are thought to be mediated by enhanced release of catecholamines, which may involve neuronal calcium influx through voltage sensitive channels. The present study examined the influence of nimodipine, a calcium channel blocker, on the DS properties of AMP. Rats (N = 8) were trained to discriminate AMP (0.5 mg/kg, IP) from saline in a two-lever, food-reinforced, drug discrimination paradigm. Nimodipine alone (2.0-5.6 mg/kg, IP) did not substitute for AMP. When given in combination with AMP, 2.0 mg/kg nimodipine increased by less than 2-fold the AMP dose necessary to induce AMP-appropriate responses. Higher doses of nimodipine combined with AMP did not increase the magnitude of this effect. Nimodipine enhanced the effects of AMP on response rate. Haloperidol (0.125 mg/kg) increased by approximately 4-fold, whereas diazepam (0.5 or 1.0 mg/kg) and morphine (5.0 mg/kg) increased by approximately 2-fold the AMP dose necessary to induce AMP-appropriate responses. The interaction with AMP was associated with enhanced reduction of response rate in the tests with diazepam and morphine but not haloperidol. These results suggest that nimodipine attenuates the DS properties of AMP, probably in a non-specific way, due to the ability of nimodipine itself to induce a discriminable internal state.
右旋苯丙胺(AMP)的辨别刺激(DS)特性被认为是由儿茶酚胺释放增强介导的,这可能涉及通过电压敏感通道的神经元钙内流。本研究考察了钙通道阻滞剂尼莫地平对AMP的DS特性的影响。在双杠杆、食物强化的药物辨别范式中,对大鼠(N = 8)进行训练,使其能够区分AMP(0.5 mg/kg,腹腔注射)和生理盐水。单独给予尼莫地平(2.0 - 5.6 mg/kg,腹腔注射)不能替代AMP。当与AMP联合给药时,2.0 mg/kg的尼莫地平使诱导AMP适当反应所需的AMP剂量增加不到2倍。更高剂量的尼莫地平与AMP联合使用并未增加这种效应的强度。尼莫地平增强了AMP对反应率的影响。氟哌啶醇(0.125 mg/kg)使诱导AMP适当反应所需的AMP剂量增加约4倍,而地西泮(0.5或1.0 mg/kg)和吗啡(5.0 mg/kg)使该剂量增加约2倍。与AMP的相互作用在使用地西泮和吗啡的试验中与反应率的增强降低相关,但在使用氟哌啶醇的试验中并非如此。这些结果表明,尼莫地平可能以非特异性方式减弱了AMP的DS特性,这是由于尼莫地平本身能够诱导一种可辨别的内部状态。