Er-Bai-Tang decoction improved the movement disorders and neuronal injury in the Parkinson's disease model rats via decreasing p38 MAPK pathway and improving the composition of intestinal flora.

IF 1.1 4区 医学 Q3 SURGERY
Jinrong Li, Yuehan Ni, Li Huang, Xinyuan Yu, Jianwei Zhu
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引用次数: 0

Abstract

Purpose: Our previous study showed that Er-Bai-Tang decoction (EBT) could effectively improve Parkinson's disease (PD) patients' quality of life, sleep, mood, and cognitive disorders, but the mechanism of EBT to treat PD was unclear. So, our study aimed to explore the mechanism of EBT to treat PD via p38 mitogen-activated protein kinases (MAPK) pathway and intestinal flora.

Methods: In our study, the PD rat model was established by subcutaneously injecting 2 mg/kg/d rotenone solution, and 23.43 g/kgEBT was used to treat PD model rats.

Results: Behavioral test showed that EBT could reverse the motor impairment in the PD model rats. Hematoxylin and eosin result showed that EBT could reduce the cell necrosis in the SNpc area of the PD model rats. Western blotting and real time-polymerase chain reaction showed that EBT could decrease the p38 MAPK expression in the SNpc area of the PD model rats. 16s rRNA sequencing analysis showed that EBT could improve the composition of intestinal flora in the PD model rats. Rikenellaceae at family level and Alistipes and Allobaculum at the genus level were the key species in the PD development and EBT treatment to PD. KEGG showed that EBT might change the iron uptake in PD rats.

Conclusions: EBT could improve the motor symptoms and neuronal injury in the PD model rat, and its mechanism may be related to decreasing p38 MAPK pathway and improving the composition of intestinal flora.

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二百汤通过降低p38 MAPK通路和改善肠道菌群组成改善帕金森病模型大鼠的运动障碍和神经元损伤。
目的:我们前期研究发现,二白汤能有效改善帕金森病患者的生活质量、睡眠、情绪和认知障碍,但其治疗PD的机制尚不清楚。因此,我们的研究旨在探讨EBT通过p38丝裂原活化蛋白激酶(MAPK)途径和肠道菌群治疗PD的机制。方法:采用鱼藤酮溶液2 mg/kg/d皮下注射的方法建立PD大鼠模型,再用23.43 g/kgEBT治疗PD模型大鼠。结果:行为学测试显示,EBT能逆转PD模型大鼠的运动障碍。苏木精和伊红结果显示,EBT能减轻PD模型大鼠SNpc区的细胞坏死。Western blotting和实时聚合酶链反应显示,EBT可降低PD模型大鼠SNpc区p38 MAPK的表达。16s rRNA测序分析显示,EBT可改善PD模型大鼠肠道菌群组成。科水平的Rikenellaceae和属水平的Alistipes和Allobaculum是PD发育和EBT治疗PD的关键物种。KEGG显示,EBT可能改变PD大鼠的铁摄取。结论:EBT可改善PD模型大鼠的运动症状和神经元损伤,其机制可能与降低p38 MAPK通路和改善肠道菌群组成有关。
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来源期刊
CiteScore
1.90
自引率
9.10%
发文量
60
审稿时长
3-8 weeks
期刊介绍: Information not localized
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