Bałkowiec-Iskra Ewa, Kurkowska-Jastrzebska Iwona, Joniec Ilona, Ciesielska Agnieszka, Członkowska Anna, Członkowski Andrzej
'Department of Experimental and Clinical Pharmacology, Medical University of Warsaw, Medical University of Warsaw, Krakowskie Przedmieście 26/28, 00-927 Warsaw, Poland.
Acta Neurobiol Exp (Wars). 2007;67(4):379-88. doi: 10.55782/ane-2007-1655.
Many data suggest involvement of inflammation in neurodegeneration. However, the exact mechanisms of this cooperation are poorly understood. We have previously shown that induction of inflammatory reaction, both before and after injury of the striatum, affects regeneration of dopaminergic neurons. In the present research we studied the role of inflammatory reaction in non-injured striatum. We used myelin oligodendrocyte glycoprotein (MOG) 35-55 in complete Freund's adjuvant (CFA) to elicit experimental autoimmune encephalomyelitis (EAE) mice model. As determined by HPLC, striatal dopamine (DA) and serotonin levels in mice treated with either MOG 35-55 in CFA or CFA alone were significantly higher compared to vehicle-treated controls on 13th day after induction. The ratio of homovanilic acid/dopamine (HVA/DA) and 3, 4 dihydroxyphenylacetic acid/dopamine (DOPAC/DA) were significantly lower in the MOG and CFA groups on 13th day, indicating decreased DA metabolism. Noradrenaline (NA) concentration did not differ between groups. Moreover, the striatal mRNA IL-1beta and TNF-alpha levels were elevated during induction phase of EAE in both groups, as determined by RT-PCR. Our data indicate regulatory connection between dopaminergic and immune systems.
许多数据表明炎症参与神经退行性变。然而,这种协同作用的确切机制尚不清楚。我们之前已经表明,在纹状体损伤之前和之后诱导炎症反应,都会影响多巴胺能神经元的再生。在本研究中,我们研究了炎症反应在未损伤纹状体中的作用。我们使用完全弗氏佐剂(CFA)中的髓鞘少突胶质细胞糖蛋白(MOG)35-55来引发实验性自身免疫性脑脊髓炎(EAE)小鼠模型。通过高效液相色谱法测定,在诱导后第13天,用CFA中的MOG 35-55或单独使用CFA处理的小鼠纹状体多巴胺(DA)和5-羟色胺水平与载体处理的对照组相比显著更高。在第13天,MOG和CFA组中高香草酸/多巴胺(HVA/DA)和3,4-二羟基苯乙酸/多巴胺(DOPAC/DA)的比率显著更低,表明DA代谢降低。去甲肾上腺素(NA)浓度在各组之间没有差异。此外,通过逆转录聚合酶链反应测定,在EAE诱导期两组纹状体mRNA白细胞介素-1β和肿瘤坏死因子-α水平均升高。我们的数据表明多巴胺能系统和免疫系统之间存在调节联系。