浙江中医药大学基础医学院
纸质出版:2014
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[1]鲍晓东,周清善.舒肌汤对帕金森病模型大鼠肌僵直的影响[J].中医杂志,2014,55(23):2034-2038.
BAO Xiaodong, ZHOU Qingshan. Effects of Shuji Decoction on Muscular Stiffness in Parkinson’s Disease Model Rats[J]. Journal of Traditional Chinese Medicine2014, 55(23): 2034-2038.
[1]鲍晓东,周清善.舒肌汤对帕金森病模型大鼠肌僵直的影响[J].中医杂志,2014,55(23):2034-2038. DOI: 10.13288/j.11-2166/r.2014.23.015.
BAO Xiaodong, ZHOU Qingshan. Effects of Shuji Decoction on Muscular Stiffness in Parkinson’s Disease Model Rats[J]. Journal of Traditional Chinese Medicine2014, 55(23): 2034-2038. DOI: 10.13288/j.11-2166/r.2014.23.015.
目的观察舒肌汤对帕金森病(PD)模型大鼠肌僵直的影响
并探讨其作用机制。方法以2μl乳胞素(1μg/μl)注射入大鼠大脑黑质部诱导PD模型大鼠24只
随机分为模型组和中药高、中、低剂量组
每组6只。以6只注射等量生理盐水大鼠作为假手术组进行比较。中药高、中、低剂量组分别给予舒肌汤40、20、10 g/(kg·d)灌胃
假手术组与模型组灌胃生理盐水20 g/(kg·d)。于给药前及给药第10、20、30天分别对各组大鼠进行爬杆测试
记录爬竿时间并进行评分
并用肌电图记录PD大鼠腓总神经电生理改变
第30天采用免疫组化染色分析黑质酪氨酸羟化酶(TH)阳性细胞的表达情况。结果与假手术组比较
模型组给药第10、20、30天的爬杆时间和评分均升高(P<0.05)
与模型组比较
中药各组给药第10、20、30天爬杆时间和评分均降低(P<0.05)
与中药中剂量组比较
中药高、低剂量组给药第10、20、30天爬杆时间和评分均升高(P<0.05)。与假手术组比较
模型组各时间点远端或近端肌肉动作电位波幅、潜伏时和神经动作电位传导速度(MCV)差异均有统计学意义(P<0.05)
与模型组比较
中药各组给药第10、20、30天远端或近端的波幅、潜伏时和MCV差异有统计学意义(P<0.05)
与中药中剂量组比较
给药第10、20、30天中药高剂量和中药低剂量组远端或近端的波幅、潜伏时和MCV差异有统计学意义(P<0.05)。与假手术组比较
模型组大鼠黑质TH阳性细胞平均光密度和阳性面积率均明显下降(P<0.05)
与模型组比较
各中药组平均光密度和阳性面积率均明显上升(P<0.05)
且中药中剂量组显著高于中药高剂量组与中药低剂量组(P<0.05)。结论舒肌汤能有效保护和修复PD模型大鼠多巴胺能神经元并且缓解肌僵直
其中以20 g/(kg·d)剂量的效果最好。
Objective To observe the effect and mechanism of Shuji Decoction on muscular stiffness in Parkinson’s disease( PD) model rats. Methods 24 PD model rats were induced by injection of 2 μl lactacystin( 1 μg /μl) into substantia nigra region
then randomly assigned to model group and high
medium
low dose Chinese medicine group
with 6 rats in each group. Six rats injecting equivalent amount of normal saline were included in sham operation group as comparison. High
medium
low dose Chinese medicine group was given Shuji Decoction 40
20
10 g /( kg·d) respectively by intragastric administration
while sham operation group and model group used saline20 g /( kg·d) by intragastric administration. On Day 0
10
20
30
pole climbing tests were carried on for each group of rats separately and electromyography( EMG) was used to record the electrophysiological change of PD rats’ common peroneal nerve. Immunohistochemical staining was used on day 30 to analyze the expression of tyrosine hydroxylase( TH) positive cells in substantia nigra. Results Compared to sham operation group
model group had increased pole-climbing time and scores( P < 0. 05) on day 10
20
30. Compared to the model group
all Chinese medicine groups had decreased pole-climbing time and scores measured on day 10
20
30( P < 0. 05). Compared with medium dose Chinese medicine group
high and low dose Chinese medicine group had increased pole-climbing time and scores on day 10
20
30( P < 0. 05). The differences of amplitude of distal or proximal muscle’s action potential
latency and motor nerve conduction velocity( MCV) in model group and sham operation group had statistical significance( P < 0. 05). The differences of amplitude of distal or proximal muscle’ s action potential
latency and MCV in model group induced at each time point had statistical significance. On day 10
20
30
the differences of amplitude of distal or proximal muscle’s action potential
latency and MCV showed statistical significance( P < 0. 05)comparing model group with all Chinese medicine groups. There were statistical significance( P < 0. 05) on the differences of medium dose Chinese medicine group and high or low dose Chinese medicine group’s record of amplitude of distal or proximal muscle’s action potential
latency and MCV on day 10
20
30. Comparing with the sham operation group
the average optical density and positive area rate of TH positive cells in nigra region in the model group decreased significantly( P < 0. 05)
while the average optical density and positive area rate in all Chinese medicine groups increased significantly( P < 0. 05) comparing with the model group
in which
middle dosege Chinese medicine group showed the best effect( P < 0. 05). Conclusion Shuji Decoction can protect and repair dopaminergic neurons in PD model rats effectively and can release muscular stiffness
with best effect achieved at the dose of 20 g /( kg·d).
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