Weissenborn R, Winn P
Department of Psychology, University of St. Andrews, Fife, UK.
Behav Brain Res. 1992 Nov 15;51(2):127-37. doi: 10.1016/s0166-4328(05)80206-2.
The effects of bilateral, N-methyl-D-aspartate (NMDA)-induced lesions of the nucleus accumbens (N.Acc.) on regulatory and behavioural responding were studied in rats and compared with the effects of bilateral 6-hydroxydopamine (6-OHDA) lesions. After postoperative body weight, food and water intake had been monitored for a period of 4 weeks, rats were tested in an exploration-choice box. Spontaneous locomotion and the locomotor and stereotypy responses to different doses of dopaminergic agonists were measured subsequently. Detailed assessment of NMDA-induced lesion volumes showed that on average 81.53% of total N.Acc. area was damaged, depending on excitotoxin dose. Tyrosine hydroxylase immunohistochemistry was used to confirm loss of mesolimbic dopamine neurones following 6-OHDA. Analysis of the behavioural data showed that NMDA N.Acc. lesions significantly enhanced exploratory behaviour, spontaneous locomotor activity and the locomotor response to a low dose of D-amphetamine. By comparison, 6-OHDA lesions did not affect exploration and spontaneous locomotion but significantly attenuated the locomotor response to a low dose of D-amphetamine. Regulatory responses were unaffected 28 days after surgery, although NMDA-lesioned rats took longer to recover from postoperative hypodipsia. The results suggest that NMDA N.Acc. lesions induce a deficit in the control of general locomotor output and are consistent with the hypothesis that the N.Acc. functions as an interface between sensory input and locomotor output and that it is needed to channel activity levels appropriately.
在大鼠中研究了伏隔核(N.Acc.)双侧 N-甲基-D-天冬氨酸(NMDA)诱导损伤对调节性和行为反应的影响,并与双侧 6-羟基多巴胺(6-OHDA)损伤的影响进行了比较。在术后对体重、食物和水摄入量进行 4 周的监测后,将大鼠置于探索选择箱中进行测试。随后测量自发运动以及对不同剂量多巴胺能激动剂的运动和刻板反应。对 NMDA 诱导损伤体积的详细评估表明,根据兴奋性毒素剂量的不同,平均有 81.53%的伏隔核总面积受到损伤。使用酪氨酸羟化酶免疫组织化学来确认 6-OHDA 后中脑边缘多巴胺神经元的损失。行为数据分析表明,NMDA 诱导的伏隔核损伤显著增强了探索行为、自发运动活动以及对低剂量 D-苯丙胺的运动反应。相比之下,6-OHDA 损伤不影响探索和自发运动,但显著减弱了对低剂量 D-苯丙胺的运动反应。尽管 NMDA 损伤的大鼠从术后低饮症中恢复所需的时间更长,但术后 28 天调节反应未受影响。结果表明,NMDA 诱导的伏隔核损伤导致一般运动输出控制方面的缺陷,这与伏隔核作为感觉输入和运动输出之间的接口发挥作用且需要适当调节活动水平的假设一致。