首页> 美国卫生研究院文献>Frontiers in Aging Neuroscience >Gami–Chunggan Formula Prevents Motor Dysfunction in MPTP/p-Induced and A53T α-Synuclein Overexpressed Parkinson’s Disease Mouse Model Though DJ-1 and BDNF Expression
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Gami–Chunggan Formula Prevents Motor Dysfunction in MPTP/p-Induced and A53T α-Synuclein Overexpressed Parkinson’s Disease Mouse Model Though DJ-1 and BDNF Expression

机译:Gami-Chunggan公式通过DJ-1和BDNF的表达阻止MPTP / p诱导的A53Tα-突触核蛋白过表达的帕金森病小鼠模型的运动功能障碍

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摘要

The Gami–Chunggan formula (GCF) is a modification of the Chunggan (CG) decoction, which has been used to treat movement disorders such as Parkinson’s disease (PD) in Traditional East Asian Medicine. To evaluate the neuroprotective effects of GCF in chronic PD animal models, we used either a 5-week treatment of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine with probenecid (MPTP/p) or the α-synuclein A53T overexpressed PD mouse model. C57BL/6 mice were treated with MPTP, in combination with probenecid, for 5 weeks. GCF was administered simultaneously with MPTP injection for 38 days. The A53T α-synuclein overexpressed mice were also fed with GCF for 60 days. Using behavioral readouts and western blot analyses, it was observed that GCF prevents motor dysfunction in the MPTP/p-induced and A53T α-synuclein overexpressed mice. Moreover, GCF inhibited the reduction of dopaminergic neurons in the substantia nigra (SN) and fibers in the striatum (ST) against MPTP/p challenge. The expression of DJ-1 was increased but that of α-synuclein was decreased in the SN of PD-like brains by GCF administration. In vitro experiments also showed that GCF inhibited 6-OHDA-induced neurotoxicity in SH-SY5Y neuroblastoma cell lines and that it did so to a greater degree than CG. Furthermore, GCF induced BDNF expression through phosphorylation of Akt, ERK, CREB, and AMPK in the SN of PD-like brains. Therefore, use of the herbal medicine GCF offers a potential remedy for neurodegenerative disorders, including Parkinson’s disease.
机译:Gami-Chunggan公式(GCF)是对Chunggan(CG)汤的改进,该汤克已用于治疗传统东亚医学中的运动障碍,例如帕金森氏病(PD)。为了评估GCF在慢性PD动物模型中的神经保护作用,我们使用了丙磺舒(MPTP / p)或1-甲基-4-苯基-1,2,3,6-四氢吡啶的5周治疗或α-突触核蛋白A53T过表达的PD小鼠模型。将C57BL / 6小鼠用MPTP结合丙磺舒治疗5周。 GCF与MPTP注射同时给药38天。 A53Tα-突触核蛋白过表达的小鼠也用GCF喂养60天。使用行为读数和蛋白质印迹分析,观察到GCF可以防止MPTP / p诱导的小鼠和A53Tα-突触核蛋白过表达的小鼠的运动功能障碍。此外,GCF抑制了黑质(SN)和纹状体(ST)中的多巴胺能神经元对MPTP / p攻击的减少。通过GCF给药,PD样脑的SN中DJ-1的表达增加,而α-突触核蛋白的表达减少。体外实验还显示,GCF在SH-SY5Y神经母细胞瘤细胞系中抑制了6-OHDA诱导的神经毒性,并且其抑制作用大于CG。此外,GCF通过PD样大脑SN中Akt,ERK,CREB和AMPK的磷酸化诱导BDNF表达。因此,使用草药GCF可为包括帕金森氏症在内的神经退行性疾病提供潜在的治疗方法。

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