Santiago M, Machado A, Cano J
Departamento de Bioquímica, Facultad de Farmacia, Universidad de Sevilla, 41012 Sevilla, Spain.
J Neurosci Methods. 2001 Jul 30;108(2):181-7. doi: 10.1016/s0165-0270(01)00390-9.
The development of a technique that allows the direct quantitative study of the damage produced by a toxin on a specific neurotransmitter system is very important. For that, we have used the microdialysis technique to validate a method to study the specific drug's toxicity on dopaminergic (DAergic) striatal terminals. We perfused different MPP(+) and 6-hydroxydopamine (6-OHDA) concentrations, with different toxicity for DAergic terminals, 24 h after the implantation of the microdialysis probe (day 1). One day later (day 2), MPP(+) was perfused through the microdialysis probe and DA extracellular output measured. We hypothesize that the amount of extracellular dopamine (DA) obtained on day 2 is directly proportional to the neurotoxic damage produced on day 1. To corroborate this hypothesis tyrosine hydroxylase (TH) immunohistochemistry was also carried out on day 2. There was a clear correlation index between the amount of DA measured after MPP(+) perfusion and the lack of TH immunoreactivity measured as the radius of the area showing decrease in TH immunoreactivity around the cannula. These results show the possibility to measure DAergic remaining terminals after a toxic drug exposure by in vivo MPP(+) perfusion. The possibility to extend this neurotoxic study to another neurotransmitter systems is suggested.
开发一种能够直接定量研究毒素对特定神经递质系统造成损伤的技术非常重要。为此,我们使用微透析技术来验证一种研究特定药物对多巴胺能(DA能)纹状体终末毒性的方法。在植入微透析探针后24小时(第1天),我们灌注了不同浓度的1-甲基-4-苯基吡啶离子(MPP(+))和6-羟基多巴胺(6-OHDA),它们对DA能终末具有不同的毒性。一天后(第2天),通过微透析探针灌注MPP(+)并测量细胞外多巴胺(DA)的输出。我们假设第2天获得的细胞外多巴胺(DA)量与第1天产生的神经毒性损伤直接相关。为了证实这一假设,在第2天还进行了酪氨酸羟化酶(TH)免疫组织化学检测。MPP(+)灌注后测得的DA量与以插管周围TH免疫反应性降低区域的半径衡量的TH免疫反应性缺失之间存在明显的相关指数。这些结果表明,通过体内MPP(+)灌注可以测量有毒药物暴露后DA能剩余终末。有人提出将这种神经毒性研究扩展到其他神经递质系统的可能性。