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Effect of cerebral dopamine neurotrophic factor on endogenous neural progenitor cell migration in a rat model of Parkinsons disease

机译:脑多巴胺神经营养因子对帕金森病大鼠模型内源性神经祖细胞迁移的影响

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摘要

This study investigated the ability of intra-subventricular zone (SVZ) administration of cerebral dopamine neurotrophic factor (CDNF) on neural progenitor cells (NPCs) attraction from the SVZ toward the 6-hydroxydopamine (6-OHDA)-lesioned striatum and improvement of motor dysfunctions in Parkinsonian rats. Male Wistar rats were assigned to four groups of the sham model (Sham), 6-OHDA-lesioned (OH), 6-OHDA-lesioned plus CDNF vehicle (OH+Vehicle), and 6-OHDA-lesioned plus CDNF (OH+CDNF). The animal model of Parkinson's disease (PD) was induced by unilateral intra-striatal infusion of 6-OHDA. Rats in the treatment groups received an intra-SVZ injection of CDNF or the vehicle of CDNF two weeks after PD model induction and were then subjected to the beam and bar tests on days 7, 14, and 21 after CDNF injection. Bromodeoxyuridine (BrdU) was intraperitoneally injected to label newly generated cells. Migration and proliferation of NPCs were assessed by BrdU/doublecortin (DCX) double immunofluorescence method on days 7, 14, and 21 after CDNF infusion. 6-OHDA in the OH group induced catalepsy and increased elapsed time in the beam test compared to the Sham group. However, administration of CDNF improved the motor performance and increased the number of DCX expressing neuroblasts in the SVZ as compared to the OH and OH+Vehicle groups. CDNF also enhanced cell proliferation and increased the number of migrated BrdU- and DCX-positive cells toward the lesioned striatum in the OH+CDNF group. These results suggest that CDNF enhances the proliferation and migration of neural stem cells (NSCs) toward the lesioned striatum accompanied by improvement of PD-induced motor dysfunctions.
机译:这项研究调查了大脑多巴胺神经营养因子(CDNF)的脑室内下区域(SVZ)施用对从SVZ向6-羟基多巴胺(6-OHDA)损伤的纹状体吸引的神经祖细胞(NPC)的能力以及运动能力的改善帕金森病大鼠的功能障碍。将雄性Wistar大鼠分为假手术模型(Sham),6-OHDA损伤(OH),6-OHDA损伤+ CDNF媒介物(OH + Vehicle)和6-OHDA损伤+ CDNF(OH + CDNF)。帕金森氏病(PD)的动物模型是通过单侧纹状体内注射6-OHDA诱导的。在PD模型诱导后两周,治疗组中的大鼠接受了SVZ内注射的CDNF或CDNF载体,然后在注射CDNF后的第7、14和21天进行束和棒测试。腹膜内注射溴脱氧尿苷(BrdU)以标记新产生的细胞。在CDNF注入后第7、14和21天,通过BrdU / doublecortin(DCX)双重免疫荧光方法评估NPC的迁移和增殖。与假手术组相比,OH组中的6-OHDA引起了僵直症,并且在射线束测试中增加了经过时间。但是,与OH和OH + Vehicle组相比,CDNF的使用改善了运动功能,并增加了SVZ中表达DCX的成神经细胞的数量。 CDNF还增强了细胞增殖,并增加了OH + CDNF组中向病变纹状体迁移的BrdU和DCX阳性细胞的数量。这些结果表明CDNF增强神经干细胞(NSCs)向病变纹状体的增殖和迁移,同时改善PD引起的运动功能障碍。

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