Carey R J, Damianopoulos E N
Department of Psychiatry, SUNY Health Science Center, Syracuse.
Behav Brain Res. 1992 Nov 15;51(2):139-47. doi: 10.1016/s0166-4328(05)80207-4.
Opponent-process theory occupies an important place in drug conditioning because it accounts for conditioned drug effects which are opposite to those induced by the drug itself. It has not been established, however, whether there is an opponent-process component to stimulant drug induced conditioned effects. In the present study the unilateral 6-hydroxydopamine (6-OHDA) rat model was used to examine this issue. Two groups of Sprague-Dawley rats with equivalent 6-OHDA lesions were administered five apomorphine treatments (0.05 mg/kg s.c.) either paired or unpaired to a 10-min test chamber placement. Apomorphine induced vigorous contralateral rotation and suppressed all ipsilateral rotation. While the apomorphine-induced contralateral rotation response can be conditioned to the test environment cues, the critical test of opponent-process theory in the present study was whether the opposite response of ipsilateral rotation would also become conditioned as a latent opponent-process response to the exteroceptive test environment cues associated with the apomorphine drug state. The postacquisition saline test for conditioning showed that the paired group exhibited higher rates of contralateral and ipsilateral rotation compared to the unpaired group. In addition, when the animals were subsequently tested with the dopaminergic receptor antagonist, haloperidol (0.5 mg/kg), unexpectedly, contralateral rotation was enhanced in the paired group, whereas, ipsilateral rotation was suppressed in both groups. While these findings are, in part, compatible with an opponent-process mechanism, the data supported a simpler explanation; namely, the mechanism of differential habituation in the two groups due to a blocking effect of apomorphine on habituation selectively in the paired group.(ABSTRACT TRUNCATED AT 250 WORDS)
对抗过程理论在药物条件作用中占据重要地位,因为它解释了与药物本身所诱导的效应相反的条件性药物效应。然而,尚未确定兴奋剂药物诱导的条件性效应中是否存在对抗过程成分。在本研究中,使用单侧6-羟基多巴胺(6-OHDA)大鼠模型来检验这个问题。两组具有等效6-OHDA损伤的Sprague-Dawley大鼠接受了五次阿扑吗啡治疗(0.05毫克/千克皮下注射),治疗与放置在10分钟测试箱中配对或不配对。阿扑吗啡诱导强烈的对侧旋转并抑制所有同侧旋转。虽然阿扑吗啡诱导的对侧旋转反应可以被条件化为测试环境线索,但本研究中对抗过程理论的关键测试是同侧旋转的相反反应是否也会作为对与阿扑吗啡药物状态相关的外感受性测试环境线索的潜在对抗过程反应而被条件化。条件作用后的生理盐水测试表明,配对组与未配对组相比,对侧和同侧旋转的发生率更高。此外,当动物随后用多巴胺能受体拮抗剂氟哌啶醇(0.5毫克/千克)进行测试时,出乎意料的是,配对组的对侧旋转增强,而两组的同侧旋转均受到抑制。虽然这些发现部分与对抗过程机制相符,但数据支持了一个更简单的解释;即,由于阿扑吗啡对配对组中习惯化的选择性阻断作用,两组中存在差异习惯化机制。(摘要截短至250字)