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Mesencephalic Astrocyte-Derived Neurotrophic Factor Is Neurorestorative in Rat Model of Parkinsons Disease

机译:中脑星形胶质细胞衍生的神经营养因子在帕金森病大鼠模型中具有神经修复作用

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摘要

Neurotrophic factors are promising candidates for the treatment of Parkinson's disease (PD). Mesencephalic astrocyte-derived neurotrophic factor (MANF) belongs to a novel evolutionarily conserved family of neurotrophic factors. We examined whether MANF has neuroprotective and neurorestorative effect in an experimental model of PD in rats. We also studied the distribution and transportation of intrastriatally injected MANF in the brain and compared it with glial cell line-derived neurotrophic factor (GDNF). Unilateral lesion of nigrostriatal dopaminergic system was induced by intrastriatal injection of 6-hydroxydopamine (6-OHDA). Amphetamine-induced turning behavior was monitored up to 12 weeks after the unilateral lesion. The local diffusion at the injection site and transportation profiles of intrastriatally injected MANF and GDNF were studied by immunohistochemical detection of the unlabeled growth factors as well as by autoradiographic and gamma counting detection of 125I-labeled trophic factors. Intrastriatally injected MANF protected nigrostriatal dopaminergic nerves from 6-OHDA-induced degeneration as evaluated by counting tyrosine hydroxylase (TH)-positive cell bodies in the substantia nigra (SN) and TH-positive fibers in the striatum. More importantly, MANF also restored the function of the nigrostriatal dopaminergic system when administered either 6 h before or 4 weeks after 6-OHDA administration in the striatum. MANF was distributed throughout the striatum more readily than GDNF. The mechanism of MANF action differs from that of GDNF because intrastriatally injected 125I-MANF was transported to the frontal cortex, whereas 125I-GDNF was transported to the SN. Our results suggest that MANF is readily distributed throughout the striatum and has significant therapeutic potential for the treatment of PD.
机译:神经营养因子有望用于治疗帕金森氏病(PD)。中脑星形胶质细胞源性神经营养因子(MANF)属于新型的神经营养因子进化保守家族。我们检查了MANF是否在大鼠PD实验模型中具有神经保护和神经修复作用。我们还研究了纹状体内注射MANF在脑中的分布和运输,并将其与胶质细胞系衍生的神经营养因子(GDNF)进行了比较。纹状体内注射6-羟基多巴胺(6-OHDA)可诱发黑质纹状体多巴胺能系统的单侧病变。在单侧病变发生后的12周内,监测苯丙胺诱导的转弯行为。通过免疫组化检测未标记的生长因子以及放射自显影和γ计数法检测 125 I标记的营养因子,研究了纹状体内注射的MANF和GDNF在注射部位的局部扩散和运输分布。通过计数黑质(SN)中的酪氨酸羟化酶(TH)阳性细胞体和纹状体中的TH阳性纤维来评估,经皮内注射的MANF保护了6-OHDA诱导的黑质纹状体多巴胺能神经。更重要的是,MANF还可以在纹状体中使用6-OHDA之前6小时或之后4周给药,恢复黑质纹状体多巴胺能系统的功能。 MANF比GDNF更容易分布在整个纹状体中。 MANF的作用机制不同于GDNF,因为纹状体内注射的 125 I-MANF被转运到额叶皮层,而 125 I-GDNF被转运到SN。我们的结果表明MANF很容易分布在整个纹状体中,并具有治疗PD的显着治疗潜力。

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