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首页> 外文期刊>Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia >High-frequency stimulation of the globus pallidus interna nucleus modulates GFRα1 gene expression in the basal ganglia.
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High-frequency stimulation of the globus pallidus interna nucleus modulates GFRα1 gene expression in the basal ganglia.

机译:高频刺激苍白球内核调节基底神经节中GFRα1基因表达。

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Deep brain stimulation (DBS) is an established therapy for movement disorders such as Parkinson's disease (PD). Although the efficacy of DBS is clear, its precise molecular mechanism remains unknown. The glial cell line derived factor (GDNF) family of ligands has been shown to confer neuroprotective effects on dopaminergic neurons, and putaminal infusion of GDNF have been investigated in PD patients with promising results. Despite the potential therapeutic role of GDNF in alleviating motor symptoms, there is no data on the effects of electrical stimulation on GDNF-family receptor (GFR) expression in the basal ganglia structures. Here, we report the effects of electrical stimulation on GFRα1 isoforms, particularly GFRα1a and GFRα1b. Wistar rats underwent 2 hours of high frequency stimulation (HFS) at the globus pallidus interna nucleus. A control group was subjected to a similar procedure but without stimulation. The HFS group, sacrificed 24 hours after treatment, had a threefold decrease in mRNA expression level of GFRα1b (p=0.037), but the expression level reverted to normal 72 hours after stimulation. Our preliminary data reveal the acute effects of HFS on splice isoforms of GFRα1, and suggest that HFS may modulate the splice isoforms of GFRα1a and GFRα1b to varying degrees. Going forward, elucidating the interactions between HFS and GFR may shed new insights into the complexity of GDNF signaling in the nervous system and lead to better design of clinical trials using these signaling pathways to halt disease progression in PD and other neurodegenerative diseases.
机译:深部脑刺激(DBS)是一种针对运动障碍(如帕金森氏病(PD))的公认疗法。尽管DBS的功效很明显,但其精确的分子机制仍然未知。已显示神经胶质细胞系衍生因子(GDNF)配体家族对多巴胺能神经元具有神经保护作用,并且已经在PD患者中研究了GDNF的鼠尾草输注,取得了可喜的结果。尽管GDNF在缓解运动症状方面具有潜在的治疗作用,但尚无电刺激对基底神经节结构中GDNF家族受体(GFR)表达的影响的数据。在这里,我们报告电刺激对GFRα1亚型,特别是GFRα1a和GFRα1b的影响。 Wistar大鼠在苍白球内部核上进行了2小时的高频刺激(HFS)。对照组接受类似的程序但没有刺激。在治疗后24小时处死的HFS组的GFRα1b的mRNA表达水平降低了三倍(p = 0.037),但是在刺激后72小时该表达水平恢复到正常。我们的初步数据揭示了HFS对GFRα1的剪接异构体的急性作用,并暗示HFS可能在不同程度上调节GFRα1a和GFRα1b的剪接异构体。展望未来,阐明HFS和GFR之间的相互作用可能会为神经系统中GDNF信号的复杂性提供新的见解,并导致使用这些信号通路阻止PD和其他神经退行性疾病的疾病进展的临床试验更好的设计。

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