Hoffman A F, van Horne C G, Eken S, Hoffer B J, Gerhardt G A
Department of Pharmacology, University of Colorado Health, Sciences Center, Denver 80262, USA.
Exp Neurol. 1997 Sep;147(1):130-41. doi: 10.1006/exnr.1997.6571.
Dopamine (DA) release and metabolism within the substantia nigra (SN) were studied in normal rats, rats with unilateral 6-hydroxydopamine (6-OHDA) lesions, and 6-OHDA-lesioned rats treated with glial cells line-derived neurotrophic factor (GDNF). Animals with > 99% DA depletions, as determined by apomorphine-induced circling behavior, also showed significant deficits in several measures of spontaneous motor activity. In vivo microdialysis recordings in the SN were carried out in normal and unilaterally 6-OHDA-lesioned rats. Basal levels of DNA were detectable only in the dialysates of normal animals, and basal levels of t he primary DA metabolites 3,4-dihydroxyphenylacetic acid and homovanillic acid were found to be significantly reduced in the SN of 6-OHDA-lesioned animals. In the presence of d-amphetamine, either alone or in combination with potassium, significant reductions in DA release were observed in the SN of 6-OHDA-lesioned animals compared to normal animals. Potassium-evoked DA release alone was not significantly different between the groups. A single intranigral administration of GDNF into 6-OHDA-lesioned animals elicited a significant reduction in apomorphine-induced rotation behavior and a significant increase in spontaneous motor activities. These behavioral changes were apparent at 1 week and persisted through 4 weeks following treatment. In vivo microdialysis showed that, although DA metabolism was altered 1 week following GDNF treatment, DA release was not significantly affected until 4 weeks following treatment.
在正常大鼠、单侧6-羟基多巴胺(6-OHDA)损伤大鼠以及用胶质细胞源性神经营养因子(GDNF)治疗的6-OHDA损伤大鼠中,研究了黑质(SN)内多巴胺(DA)的释放和代谢。通过阿扑吗啡诱导的转圈行为确定DA耗竭>99%的动物,在几种自发运动活动指标上也表现出显著缺陷。在正常和单侧6-OHDA损伤大鼠中对SN进行了体内微透析记录。仅在正常动物的透析液中可检测到DA的基础水平,并且发现在6-OHDA损伤动物的SN中,主要DA代谢产物3,4-二羟基苯乙酸和高香草酸的基础水平显著降低。与正常动物相比,在6-OHDA损伤动物的SN中,单独或与钾联合使用d-苯丙胺时,观察到DA释放显著减少。两组之间单独由钾诱发的DA释放没有显著差异。向6-OHDA损伤动物单次脑内注射GDNF可显著减少阿扑吗啡诱导的旋转行为,并显著增加自发运动活动。这些行为变化在治疗后1周明显,并持续到4周。体内微透析显示,尽管GDNF治疗后1周DA代谢发生改变,但直到治疗后4周DA释放才受到显著影响。