Dentresangle C, Le Cavorsin M, Savasta M, Leviel V
Laboratoire de Neuropharmacologie Moléculaire, CNRS UMR 5542, Rue Guillaume Paradin, 69372 Cedex 8, Lyon, France
Brain Res. 2001 Mar 2;893(1-2):178-85. doi: 10.1016/s0006-8993(00)03311-4.
After injection of 6-hydroxydopamine into the lateral part of the rat substantia nigra, tissue dopamine (DA), dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) were reduced in the corresponding lateral part of the ipsilateral caudate/putamen (CP) complex (13, 40 and 56% of controls, respectively). In this region, tyrosine hydroxylase (TH, the rate limiting enzyme of the DA synthesis) immunoautoradiography decreased by more than 80% as was the case for the binding of tritiated GBR12935 (a specific marker of the DA-carrier protein). In the medial region of the CP, only very moderate reductions of DA, DOPAC and HVA (77, 76 and 84% of controls, respectively) were observed. In this region, TH immunoautoradiography and GBR12935 binding were only reduced by about 20% reflecting weak DA denervation. However, using in vivo voltammetry, extracellular basal DA levels were found to be particularly high in the medial region of CP complex when compared to unoperated animals (up to 235%). In the medial region, TH activity was also significantly increased (161%) but the electrical stimulation of DA fibers produced the same DA overflow in control and lesioned animals. From these results, it may be concluded that elevated basal DA levels in this region cannot be attributed to the reduced DA uptake and/or to an increased ability of DA neurons to release DA in response to impulse flow.
将6-羟基多巴胺注射到大鼠黑质外侧部后,同侧尾状核/壳核(CP)复合体相应外侧部的组织多巴胺(DA)、二羟基苯乙酸(DOPAC)和高香草酸(HVA)减少(分别为对照组的13%、40%和56%)。在该区域,酪氨酸羟化酶(TH,DA合成的限速酶)免疫放射自显影减少超过80%,氚标记的GBR12935(DA载体蛋白的特异性标记物)结合情况也是如此。在CP的内侧区域,仅观察到DA、DOPAC和HVA非常适度的减少(分别为对照组的77%、76%和84%)。在该区域,TH免疫放射自显影和GBR12935结合仅减少约20%,反映出DA去神经支配较弱。然而,使用体内伏安法发现,与未手术动物相比,CP复合体内侧区域的细胞外基础DA水平特别高(高达235%)。在内侧区域,TH活性也显著增加(161%),但DA纤维的电刺激在对照动物和损伤动物中产生的DA溢出相同。从这些结果可以得出结论,该区域基础DA水平升高不能归因于DA摄取减少和/或DA神经元响应冲动流释放DA的能力增加。