Corrigall W A, Linseman M A, D'Onofrio R M, Lei H
Psychopharmacology (Berl). 1986;89(3):327-33. doi: 10.1007/BF00174369.
A previously reported paradigm in which rats run down a runway for food reward followed by morphine injection was analyzed to assess the utility of the paradigm in studies of opiate reinforcement. One experiment replicated the original report that post-trial morphine caused both an increase in runway speed and a decrease in food consumption (taste aversion) over successive trials, and showed in addition that the increase in runway speed did not occur as a result of food deprivation alone, but required the animals to have consumed food in the goal box. A second study using the quaternary opiate antagonist methyl naltrexone to block the peripheral effects of morphine suggested that the increase in runway speed has a peripheral locus while the taste aversion has a central one. A third experiment in which morphine was microinjected into either the lateral ventricle or the ventral tegmental area supported these observations, in that intracranial morphine failed to result in an increased runway speed, but did produce taste aversion after microinjection into either site. These findings also suggest that the increase in runway speed caused by post-trial morphine in this experiment has a peripheral locus of effect, which is probably distinct from the central effect that supports morphine self-administration and conditioned place preference.
对先前报道的一种实验范式进行了分析,该范式中大鼠跑下跑道获取食物奖励,随后注射吗啡,以评估该范式在阿片类强化研究中的效用。一项实验重复了最初的报告,即试验后注射吗啡会导致连续试验中跑道速度增加和食物消耗减少(味觉厌恶),此外还表明,跑道速度的增加并非仅由食物剥夺导致,而是要求动物在目标箱中进食。第二项研究使用四价阿片拮抗剂甲基纳曲酮来阻断吗啡的外周效应,结果表明跑道速度的增加具有外周作用位点,而味觉厌恶具有中枢作用位点。第三项实验将吗啡微量注射到侧脑室或腹侧被盖区,支持了这些观察结果,因为颅内注射吗啡未能导致跑道速度增加,但在注射到任何一个部位后都产生了味觉厌恶。这些发现还表明,本实验中试验后注射吗啡导致的跑道速度增加具有外周作用位点,这可能与支持吗啡自我给药和条件性位置偏好的中枢作用不同。