Carlson J N, Visker K E, Keller R W, Glick S D
Department of Pharmacology and Neuroscience, Albany Medical College, NY 12208, USA.
Brain Res. 1996 Mar 4;711(1-2):1-9. doi: 10.1016/0006-8993(95)01290-7.
The effects of left and right prefrontal cortical dopamine (DA) depletion on circling behavior, stress-escape behavior and subcortical DA function were examined in rats exhibiting left or right turning biases. 6-Hydroxydopamine lesions of the medial prefrontal cortex (PFC) caused significant DA depletions when assessed in separate studies at 3 days and 3-4 weeks. However, depletions were smaller at 3-4 weeks and there was a significant increase in DA concentration on the left side following right lesions. Significant increases in striatal DA content were observed following lesions of either side at 3-4 weeks, but not at 3 days. No changes in DA concentration were observed in the nucleus accumbens septi (NAS). Left circling rats significantly increased their circling behavior following right sided lesions and showed disrupted footshock-escape behavior following left sided lesions. Performance of the footshock-escape task exerted an effect on striatal and NAS DA utilization as indicated by the ratio of 3,4-dihydroxyphenylacetic acid (DOPAC) to DA. The effects of footshock on NAS DA utilization were greater following left PFC lesions as compared to the right lesion and sham conditions. These lesion effects were also greater in left- than in right-turning animals. The data indicate that an intrinsic asymmetry in brain DA systems interacts with left and right PFC lesions to differentially determine subcortical DA function and behaviors that it subserves.
在表现出左旋或右旋偏好的大鼠中,研究了左、右前额叶皮质多巴胺(DA)耗竭对转圈行为、应激逃避行为和皮质下DA功能的影响。在3天和3 - 4周的单独研究中评估时,内侧前额叶皮质(PFC)的6 - 羟基多巴胺损伤导致显著的DA耗竭。然而,在3 - 4周时耗竭较小,右侧损伤后左侧的DA浓度显著增加。在3 - 4周时,两侧损伤后纹状体DA含量均显著增加,但在3天时未观察到。伏隔核(NAS)中的DA浓度未观察到变化。左旋大鼠在右侧损伤后显著增加其转圈行为,在左侧损伤后表现出电击逃避行为受损。如3,4 - 二羟基苯乙酸(DOPAC)与DA的比率所示,电击逃避任务的表现对纹状体和NAS的DA利用产生影响。与右侧损伤和假手术条件相比,左侧PFC损伤后电击对NAS DA利用的影响更大。这些损伤效应在左旋动物中也比右旋动物中更大。数据表明,脑DA系统中的内在不对称性与左、右PFC损伤相互作用,以差异方式决定皮质下DA功能及其所支持的行为。