Cenci M A, Björklund A
Department of Medical Cell Research, University of Lund, Sweden.
Eur J Neurosci. 1993 Aug 1;5(8):1062-70. doi: 10.1111/j.1460-9568.1993.tb00959.x.
Corticofugal fibres from the prefrontal, prelimbic and anterior sensorimotor cortices were transected by a wide coronal knife-cut through the forceps minor. The cut was performed on the dopamine-depleted side of unilaterally 6-hydroxydopamine-lesioned rats, or on either the right or the left side of intact rats. Sham-lesioned controls received a superficial cortical cut at the same level. Seven days after surgery, apomorphine (0.25 mg/kg s.c.) was administered to 6-hydroxydopamine-lesioned animals and D-amphetamine (5 mg/kg i.p.) was administered to the non-dopamine-denervated ones. Two hours later, the animals were perfusion-fixed for the immunohistochemical detection of the nuclear protein Fos. A computerized image analysis technique was used to quantify, bilaterally, striatal Fos expression in 11 areas of the striatum. The frontocortical transection reduced both apomorphine- and amphetamine-induced Fos expression by 33-66% within the ipsilateral caudate-putamen. The effect was observed throughout the rostral portion of the striatal complex, where the lesioned cortical fibres terminate most densely. A separate batch of unilaterally 6-hydroxydopamine-lesioned rats were used to test the effect of frontocortical transection on amphetamine- and apomorphine-induced turning behaviour. Two groups of rats, showing similar rates of contralateral turning (7-8 turns/min) in response to apomorphine (0.25 mg/kg s.c.), were subjected to either a complete frontocortical transection or a sham lesion on the dopamine-denervated side. An additional two groups, showing comparable rates of ipsilateral turning (15 turns/min) in response to amphetamine (5 mg/kg i.p.), received similar lesions, but now on the side ipsilateral to the intact dopaminergic innervation.(ABSTRACT TRUNCATED AT 250 WORDS)
来自前额叶、前边缘叶和前感觉运动皮层的皮质离心纤维通过一把宽冠状刀切断,切断部位在胼胝体小钳处。切断操作在单侧6-羟基多巴胺损伤大鼠的多巴胺耗竭侧进行,或者在完整大鼠的右侧或左侧进行。假损伤对照组在相同水平进行浅表皮质切割。手术后7天,给6-羟基多巴胺损伤的动物皮下注射阿扑吗啡(0.25mg/kg),给未去多巴胺神经支配的动物腹腔注射D-苯丙胺(5mg/kg)。两小时后,对动物进行灌注固定,用于免疫组织化学检测核蛋白Fos。使用计算机图像分析技术对纹状体11个区域的双侧纹状体Fos表达进行定量。前额叶皮质横断使同侧尾状核-壳核内阿扑吗啡和苯丙胺诱导的Fos表达降低了33%-66%。在纹状体复合体的整个前部均观察到了这种效应,受损的皮质纤维在该区域终止最为密集。另一批单侧6-羟基多巴胺损伤的大鼠用于测试前额叶皮质横断对苯丙胺和阿扑吗啡诱导的旋转行为的影响。两组对阿扑吗啡(0.25mg/kg皮下注射)有相似对侧旋转速率(7-8转/分钟)的大鼠,在多巴胺去神经支配侧分别进行完全前额叶皮质横断或假损伤。另外两组对苯丙胺(5mg/kg腹腔注射)有相似同侧旋转速率(15转/分钟)的大鼠,接受类似的损伤,但损伤部位在与完整多巴胺能神经支配同侧的一侧。(摘要截断于250字)