Comparison of the effects of morphine, pentazocine, cyclazocine and amphetamine on intracranial self-stimulation in the rat.

S G Holtzman
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引用次数: 23

Abstract

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.

吗啡、戊唑嗪、环唑嗪和安非他明对大鼠颅内自我刺激作用的比较。
老鼠被训练按下杠杆,通过长期植入的电极刺激它们的下丘脑。测定吗啡(0.3 ~ 10mg /kg)、戊唑嗪(1.0 ~ 30mg /kg)、环唑嗪(0.03 ~ 30mg /kg)、d-安非他明(0.1 ~ 3.0 mg/kg)对颅内刺激反应的剂量-反应曲线,并在纳洛酮1 ~ 2剂量下重新测定。这三种镇痛药仅产生剂量相关的降低,其相对效力如下:环唑辛大于吗啡,戊唑辛大于戊唑辛。d-安非他明在0.3和1.0 mg/kg剂量下对颅内自我刺激有明显的加速作用;3.0 mg/kg时反应降低与刻板行为有关。纳洛酮本身对自我刺激没有影响,但增加了抑制反应率所需的镇痛药剂量,这与竞争性拮抗作用一致。相比之下,在纳洛酮存在的情况下,所有剂量的d-安非他明的反应率测试。因此,纳洛酮与d-安非他明的相互作用与纳洛酮与镇痛药的相互作用有质的不同。这一发现延伸到颅内自我刺激,这是之前关于d-安非他明和纳洛酮对大鼠行为相互作用的报道的普遍性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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