Segovia J, Tillakaratne N J, Whelan K, Tobin A J, Gale K
Department of Pharmacology, Georgetown University Medical Center, Washington, D.C. 20007.
Brain Res. 1990 Oct 8;529(1-2):345-8. doi: 10.1016/0006-8993(90)90849-7.
Adult male rats were lesioned with 6-hydroxydopamine in order to destroy the nigrostriatal dopaminergic projections. In rats with such a lesion, we found a parallel increase in glutamic acid decarboxylase (GAD) activity and GAD mRNA in the striatum ipsilateral to the lesion at 4 weeks and 4 months after the lesion. These observations support the proposal that nigral dopaminergic neurons exert a tonic inhibitory control over the striatal GABAergic neurons. Our observations also suggest that the dopaminergic neurons can inhibit gene expression in striatal GABAergic neurons and that the enhanced striatal GAD activity following lesions of the dopaminergic projections is due to 'de novo' synthesis of the enzyme.
成年雄性大鼠用6-羟基多巴胺进行损伤,以破坏黑质纹状体多巴胺能投射。在有这种损伤的大鼠中,我们发现在损伤后4周和4个月时,损伤同侧纹状体中的谷氨酸脱羧酶(GAD)活性和GAD mRNA平行增加。这些观察结果支持以下观点,即黑质多巴胺能神经元对纹状体GABA能神经元施加紧张性抑制控制。我们的观察结果还表明,多巴胺能神经元可以抑制纹状体GABA能神经元中的基因表达,并且多巴胺能投射损伤后纹状体GAD活性增强是由于该酶的“从头”合成。