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

机译:脑多巴胺神经营养因子对帕金森病大鼠内源神经祖细胞迁移的影响

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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:本研究研究了子宫内区(SVZ)脑多巴胺神经营养因子(CDNF)对神经祖细胞(NPC)施用的能力从SVZ朝向6-羟基多氨基胺(6-OHDA)的纹状体和电动机的改进帕金森大鼠的功能障碍。将雄性Wistar大鼠分配到四组假模型(假),6- OHDA-损失(OH),6-OHDA-损失加入CDNF载体(OH +载体),6-OHDA-LESIONED加入CDNF(OH + CDNF)。帕金森病(PD)的动物模型由6-OHDA的单侧脊髓内输注诱导。治疗组中的大鼠在PD模型诱导后两周内接受了SVZ的CDNF或CDNF的载体,然后在CDNF注射后的第7,14和21天进行梁和杆测试。溴过氧亚氨基(Brdu)腹膜内注射以标记新产生的细胞。通过在CDNF输注后的第7,14和21天,通过BRDU / DOPCRETIN(DCX)双免疫荧光法评估NPC的迁移和增殖。与假手术组相比,OH组在OH组诱导的Catalepsy和梁测试中的经过时间增加。然而,与OH和OH +载体基团相比,CDNF的给药改善了电动机性能并增加了SVZ中表达神经细胞的DCx的数量。 CDNF还增强了细胞增殖,并使迁移的BRDU和DCX阳性细胞朝向OH + CDNF组的损伤纹状体增加。这些结果表明CDNF通过改善PD诱导的电动机功能障碍的改善,CDNF增强神经干细胞(NSCs)的增殖和迁移。

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