Forni C, Brundin P, Strecker R E, el Ganouni S, Björklund A, Nieoullon A
Laboratoire de Neurosciences Fonctionnelles, CNRS, Marseille, France.
Exp Brain Res. 1989;76(1):75-87. doi: 10.1007/BF00253625.
In vivo voltammetry was used to monitor dopamine (DA) neuron activity during the course of reinnervation of the initially denervated caudate-putamen by grafted mesencephalic neurons. Fetal DA neurons were implanted as a cell suspension into the depth of the caudate-putamen in adult 6-hydroxy-dopamine-lesioned recipient rats. Recordings were performed over a period of 2.5-4 months, starting within a week after transplantation, using chronically implanted surface-treated multifiber carbon electrodes. The voltammetric method used in this study has generated considerable discussion centred on the ability of the multifiber electrodes to measure DA alone in vivo, but the results of previous studies have led to the conclusion that changes in the voltammetric signal most probably reflect dopaminergic terminal activity. It seems therefore possible to follow the time-course of changes in the voltammetric signal amplitude during the process of dopaminergic reinnervation of the host striatum from the grafts. A 6-hydroxydopamine lesion of the mesostriatal dopamine pathway caused a substantial (greater than 80%) reduction of the voltammetric signal within 8-10 days, and the low residual signal remained essentially unchanged for time periods up to at least 5 months in the non-grafted control rats. In 7 of 11 rats with DA-rich grafts there was a recovery of the signal amplitude to levels within, or close to, the range recorded from the striatum of normal intact rats. The increase was observed 6-8 weeks after grafting in the rats which had received the largest transplants, and at about 13-14 weeks after grafting in the rats which had received the smallest ones. The recovery of the signal amplitude, from baseline to maximal response, was quite rapid and typically developed between two or three recording sessions, i.e. over a period of one to two weeks. In contrast to the intact striatum, the recovered signal in the graft-reinnervated striata showed a progressive decline within one hour of sampling time at high sampling frequencies (1 per min to 1 per 3 min). Grafted striata also showed a larger response to systemically administered amphetamine than did intact striata. Since the changes in the voltammetric signal recorded with the multifiber electrode mainly reflect dopaminergic terminal activity, the results provide evidence that the intrastriatal DA-rich grafts are spontaneously active, and that the grafted DA neurons can restore DA neuro-transmission in the reinnervated part of the host caudate-putamen to levels which are within the normal range.(ABSTRACT TRUNCATED AT 400 WORDS)
在移植的中脑神经元对最初去神经支配的尾状核-壳核进行再支配的过程中,采用体内伏安法监测多巴胺(DA)能神经元的活性。将胎鼠DA能神经元作为细胞悬液植入成年6-羟基多巴胺损伤受体大鼠的尾状核-壳核深部。记录从移植后一周内开始,持续2.5 - 4个月,使用长期植入的经表面处理的多纤维碳电极。本研究中使用的伏安法引发了大量讨论,焦点在于多纤维电极在体内单独测量DA的能力,但先前研究结果得出结论,伏安信号的变化很可能反映了多巴胺能终末的活性。因此,似乎有可能追踪移植后宿主纹状体多巴胺能再支配过程中伏安信号幅度变化的时间进程。中脑-纹状体多巴胺通路的6-羟基多巴胺损伤在8 - 10天内导致伏安信号大幅降低(超过80%),在未移植的对照大鼠中,低残留信号在长达至少5个月的时间内基本保持不变。在11只植入富含DA移植物的大鼠中,有7只的信号幅度恢复到正常完整大鼠纹状体记录的范围内或接近该范围。在接受最大移植量的大鼠中,移植后6 - 8周观察到信号增加;在接受最小移植量的大鼠中,移植后约13 - 14周观察到信号增加。信号幅度从基线恢复到最大反应相当迅速,通常在两到三次记录期间即一到两周内出现。与完整纹状体不同,在高采样频率(每分钟1次至每3分钟1次)下,移植再支配纹状体中恢复的信号在采样时间的一小时内显示出逐渐下降。移植的纹状体对全身给予的苯丙胺的反应也比完整纹状体更大。由于用多纤维电极记录的伏安信号变化主要反映多巴胺能终末的活性,这些结果提供了证据,表明纹状体内富含DA的移植物具有自发活性,并且移植的DA能神经元可以将宿主尾状核-壳核再支配部分的DA神经传递恢复到正常范围内的水平。(摘要截选至400字)