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麻醉性镇痛药对大鼠颅内自我刺激的剂量和时间依赖性影响。

Dose- and time-dependent effects of narcotic analgesics on intracranial self-stimulation in the rat.

作者信息

Schaefer G J, Holtzman S G

出版信息

Psychopharmacology (Berl). 1977 Aug 16;53(3):227-34. doi: 10.1007/BF00492356.

Abstract

Rats were trained to bar-press in order to obtain electrical stimulation of the medial forebrain bundle through chronically implanted electrodes. Dose-response and time-effect curves were determined for morphine (1.0-30 mg/kg), levorphanol (0.1 to 3.0 mg/kg), methadone (0.1-3.0 mg/kg), meperidine (1.0-30 mg/kg), oxymorphone (0.03-1.0 mg/kg), and d-amphetamine (0.1-3.0 mg/kg). Dose-response and time-effect curves were also determined for morphine (1.0-30 mg/kg) in rats that had received multiple injections of morphine over a period of 3 days. All of the narcotic analgesics produced dose-related decreases in responding; the durations of these decreases were also dose-related. The relative potencies of the five narcotic analgesics with respect to the rate-decreasing effects for selt-stimulation responding were: oxymorphone greater than levorphanol greater than methadone greater than morphine greater than meperidine. In morphine-tolerant rats the rate-decreasing effects of morphine on responding for selt-stimulation were attenuated. These findings suggest that narcotic analgesics from diverse chemical families have a similar, predominantly depressant, effect on self-stimulation behavior and that the relative potencies of a series of narcotics for this effect are similar to those demonstrated for other properties of these drugs.

摘要

通过长期植入电极,训练大鼠按压杠杆以获得内侧前脑束的电刺激。测定了吗啡(1.0 - 30毫克/千克)、左啡诺(0.1至3.0毫克/千克)、美沙酮(0.1 - 3.0毫克/千克)、哌替啶(1.0 - 30毫克/千克)、羟吗啡酮(0.03 - 1.0毫克/千克)和右旋苯丙胺(0.1 - 3.0毫克/千克)的剂量反应曲线和时效曲线。还测定了在3天内接受多次吗啡注射的大鼠中吗啡(1.0 - 30毫克/千克)的剂量反应曲线和时效曲线。所有麻醉性镇痛药均产生与剂量相关的反应减少;这些减少的持续时间也与剂量相关。五种麻醉性镇痛药对自身刺激反应的速率降低作用的相对效价为:羟吗啡酮大于左啡诺大于美沙酮大于吗啡大于哌替啶。在吗啡耐受的大鼠中,吗啡对自身刺激反应的速率降低作用减弱。这些发现表明,来自不同化学家族的麻醉性镇痛药对自我刺激行为具有相似的、主要为抑制性的作用,并且一系列麻醉药对此作用的相对效价与这些药物的其他特性所显示的效价相似。

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