运动干预对PD小鼠皮质纹状体突触传递效率的影响

G-A Zhao, Danyu Zhang, D. Qiao, Xiaoli Liu
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This experiment will use the patch clamp to explore the effect of exercise intervention on the synaptic transmission efficiency of cortical-striatum in PD mice. \nMethods The experimental animals (C57 mice male, 4 weeks) were randomly divided into normal group(N), PD group(PD)and PD exercise group(PD+EX).PD mice models were established by injection of 6-OHDA in the striatum (4μg/position, AP + 0.5mm ML - 1.8mm DV - 3.0mm and- 2.0mm). Apomorphine(APO) rotation experiments were performed one week later to identify the model. The formal exercise intervention program was 16m/min, 40min/d, 5d/week,4 weeks(after the adaptive training, total of five weeks of treadmill exercise). At the end of the intervention, brain slices (350μm) were prepared from each group of mice. 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摘要

目的帕金森病(PD)是一种由黑质致密部多巴胺能神经元变性和纹状体多巴胺水平下降引起的神经退行性疾病。既往研究证实纹状体功能障碍是PD小鼠行为功能障碍的重要原因,皮层-纹状体突触传递的改变可能在PD病理中起重要作用。本实验将利用膜片钳探讨运动干预对PD小鼠皮质纹状体突触传递效率的影响。方法实验动物(雄性C57小鼠,4周龄)随机分为正常组(N)、PD组(PD)和PD运动组(PD+EX)。通过纹状体注射6-OHDA (4μg/位,AP + 0.5mm ML - 1.8mm DV - 3.0mm和- 2.0mm)建立PD小鼠模型。1周后进行阿波啡(Apomorphine, APO)旋转实验以鉴定模型。正式运动干预方案为16m/min、40min/d、5d/周、4周(适应性训练结束后,共进行5周的跑步机运动)。在干预结束时,从每组小鼠制备350μm的脑切片。记录纹状体最大场兴奋性突触后电位(fEPSP)和刺激强度增加时纹状体的fEPSP。结果1。APO旋转实验结果:PD模型小鼠16/21(比标准高205.25±36.46 r)。2.N只小鼠fEPSP最大振幅为1.9199±0.213mv(N =8), PD为1.0129±0.140 mv(N =8);PD +例:1.3221±.0865mv (n = 8)。组间差异有统计学意义(P<0.05)。3.PD组小鼠的I-O曲线斜率较N组小鼠明显减小。与PD小鼠相比,PD+EX小鼠的I-O曲线斜率增大(P<0.05)。结论1。成功建立6-OHDA诱导PD模型。PD病理状态下纹状体功能异常,运动干预可增强纹状体活性。2. PD状态下皮层-纹状体突触传递效率降低,运动干预提高了皮层-纹状体突触传递效率。
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PO-160 Effect of exercise intervention on the synaptic transmission efficiency of cortical-striatum in PD mice
Objective Parkinson's disease (PD) is a neurodegenerative disease caused by degeneration of dopaminergic neurons in the substantia nigra pars compacta and decreased levels of striatal dopamine. Previous studies have confirmed that striatum dysfunction is an important cause of behavioral dysfunction in PD mice, and changes in cortical-striatum synaptic transmission may play an important role in PD pathology. This experiment will use the patch clamp to explore the effect of exercise intervention on the synaptic transmission efficiency of cortical-striatum in PD mice. Methods The experimental animals (C57 mice male, 4 weeks) were randomly divided into normal group(N), PD group(PD)and PD exercise group(PD+EX).PD mice models were established by injection of 6-OHDA in the striatum (4μg/position, AP + 0.5mm ML - 1.8mm DV - 3.0mm and- 2.0mm). Apomorphine(APO) rotation experiments were performed one week later to identify the model. The formal exercise intervention program was 16m/min, 40min/d, 5d/week,4 weeks(after the adaptive training, total of five weeks of treadmill exercise). At the end of the intervention, brain slices (350μm) were prepared from each group of mice. The maximum striatum fEPSP (field excitatory postsynaptic potential, fEPSP) and striatum fEPSP under increasing stimulation intensity were recorded. Results 1.The results of APO rotation experiment: PD mice modeled 16/21(205.25±36.46 r higher than the standard). 2.N mice the maximum fEPSP amplitude is 1.9199±0.213mv(n=8);PD: 1.0129±0.140 mv(n=8); PD+EX: 1.3221±.0865mv(n=8).There are significant differences between groups(P<0.05). 3. There is a significant decrease in the slope of I-O curve in the PD mice compared with the N mice. And compared with the PD mice, the slope of I-O curve in PD+EX mice was increase(P<0.05). Conclusions 1. 6-OHDA induced PD model was successfully established. The striatum function was abnormal in the pathological state of PD, and the exercise intervention enhanced the activity of the striatum. 2. The cortical-striatum synaptic transmission efficiency is reduced in the PD state, and the exercise intervention improved the cortical-striatum synaptic transmission efficiency.
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