Holtzman S G
Psychopharmacologia. 1976 Apr 15;46(3):223-7. doi: 10.1007/BF00421106.
Rats were trained to press a lever in order to stimulate their hypothalamus through a chronically implanted electrode. Dose-response curves were determined for the effects of morphine (0.3-10 mg/kg), pentazocine (1.0-30 mg/kg), cyclazocine (0.03-30 mg/kg) and d-amphetamine (0.1-3.0 mg/kg) on responding for intracranial stimulation, and then were redetermined in the presence of one or two doses of naloxone. The three analgesics produced only dose-related decreases in responding with the following relative potencies: cyclazocine greater than morphine greater than pentazocine. The well-documented rate-increasing effects of d-amphetamine on intracranial self-stimulation were observed at 0.3 and 1.0 mg/kg of the drug; decreases in responding at 3.0 mg/kg were associated with stereotyped behavior. Naloxone, which had no effect of its own on self-stimulation, increased the dose of the analgesics required to depress response rate in a manner consistent with a competitive antagonism. In contrast, response rates at all doses of d-amphetamine tested in the presence of naloxone. Thus, the interaction between naloxone and d-amphetamine is qualitatively different from the one between naloxone and the analgesics. This finding extends to intracranial self-stimulation the generality of a previous report of interactions between d-amphetamine and naloxone on behavior in the rat.
训练大鼠按压杠杆,以便通过长期植入的电极刺激其下丘脑。测定吗啡(0.3 - 10毫克/千克)、喷他佐辛(1.0 - 30毫克/千克)、环唑辛(0.03 - 30毫克/千克)和右旋苯丙胺(0.1 - 3.0毫克/千克)对颅内刺激反应的剂量 - 反应曲线,然后在存在一或两个剂量纳洛酮的情况下重新测定。这三种镇痛药仅产生与剂量相关的反应减少,其相对效力如下:环唑辛大于吗啡大于喷他佐辛。在药物剂量为0.3和1.0毫克/千克时观察到右旋苯丙胺对颅内自我刺激有充分记录的速率增加作用;在3.0毫克/千克时反应减少与刻板行为有关。纳洛酮本身对自我刺激没有影响,它以与竞争性拮抗作用一致的方式增加了抑制反应速率所需的镇痛药剂量。相比之下,在纳洛酮存在下测试的所有剂量的右旋苯丙胺的反应速率……(原文此处似乎不完整)。因此,纳洛酮与右旋苯丙胺之间的相互作用在性质上与纳洛酮与镇痛药之间的相互作用不同。这一发现将右旋苯丙胺与纳洛酮之间对大鼠行为相互作用的先前报道的普遍性扩展到了颅内自我刺激。