Oliveras J L, Maixner W, Dubner R, Bushnell M C, Kenshalo D R, Duncan G H, Thomas D A, Bates R
J Neurosci. 1986 Oct;6(10):3086-93. doi: 10.1523/JNEUROSCI.06-10-03086.1986.
We examined the effects of morphine microinjected into the medullary dorsal horn (MDH) on the ability of monkeys to detect temperature increases in the noxious heat range. Behavioral detection latency and the percentage of correct detections were used as measures of the perceived intensity of noxious heat stimuli. Three monkeys were trained to detect a change (T2) of 0.4, 0.6, or 1.0 degrees C from a previous noxious heat level of 46 degrees C (T1). Effects on attentional, motivational, and motoric aspects of the monkeys' behavior were assessed by having them detect innocuous cooling and visual stimuli in tasks of similar difficulty. Morphine (1, 3, and 10 micrograms) microinjected into the MDH produced a dose-dependent and stimulus-intensity-dependent increase in the latency to detection of the T2 stimuli. These effects were opiate receptor-mediated since they were antagonized by systemically administered naloxone (0.5 mg/kg, i.m.) given 40 min after the microinjection of morphine. There were no effects of morphine on the behavioral detection latencies to the innocuous cooling and visual stimuli, indicating that the effects of morphine were modality-specific and independent of changes in motivation, attention, or motoric ability. These data demonstrate a pharmacologically specific effect of opiates on the perceived intensity of noxious heat stimuli at the earliest central relay pathway transmitting noxious information.
我们研究了向延髓背角(MDH)微量注射吗啡对猴子检测有害热范围内温度升高能力的影响。行为检测潜伏期和正确检测的百分比被用作有害热刺激感知强度的指标。三只猴子经过训练,以检测相对于先前46摄氏度(T1)的有害热水平0.4、0.6或1.0摄氏度的变化(T2)。通过让它们在难度相似的任务中检测无害冷却和视觉刺激,评估对猴子行为的注意力、动机和运动方面的影响。向MDH微量注射吗啡(1、3和10微克)会导致检测T2刺激的潜伏期出现剂量依赖性和刺激强度依赖性增加。这些效应是由阿片受体介导的,因为在微量注射吗啡40分钟后全身给予纳洛酮(0.5毫克/千克,肌肉注射)可拮抗这些效应。吗啡对无害冷却和视觉刺激的行为检测潜伏期没有影响,表明吗啡的作用具有模式特异性,且与动机、注意力或运动能力的变化无关。这些数据证明了阿片类药物在传递有害信息的最早中枢中继途径上对有害热刺激感知强度具有药理学特异性作用。