CHEN Song-sheng, LI Chen, YANG Ying, et al. Protective Effects and Mechanism of Bushen Houxue Fang on Parkinson's Disease Rat Dopaminergic Neurons[J]. Chinese journal of experimental traditional medical formulae, 2014, 20(21): 175-179.
DOI:
CHEN Song-sheng, LI Chen, YANG Ying, et al. Protective Effects and Mechanism of Bushen Houxue Fang on Parkinson's Disease Rat Dopaminergic Neurons[J]. Chinese journal of experimental traditional medical formulae, 2014, 20(21): 175-179. DOI: 10.13422/j.cnki.syfjx.2014210175.
Protective Effects and Mechanism of Bushen Houxue Fang on Parkinson's Disease Rat Dopaminergic Neurons
Objective: Observe the protective effects of Bushen Houxue fang(BSHXF) on 6-hydroxydopamine (6-OHDA) type of Parkinson's disease in substantia nigra of injection of 6-OHD rat dopaminergic neurons. Method: Substantia nigra once injection of 4 μL 6-OHDA to model the Parkinson's disease rat
and divide those models into 6 different groups: normal control (0.9% NaCl)model (0.9% NaCl)
madopar comparison (20 mg·kg-1 madopar)
high (15 g·kg-1 BSHXF)
mid (10 g·kg-1) and low (5 g·kg-1) dosage of BSHXF. Each group intragastric administration one time every day for 15 days. Using ethology detection
immunohistochemistry to determine substantia nigra tyrosine hydroxylase
SOD
MDA and GSH-Px
then observe the protective effects of Bushen Houxue fang on DA neurons. Result: ①Group model rotates clockwise (11.27±1.68) lap/min
there is significant difference (P<0.05) among High dosage of BSHXF group (6.35± 1.49 lap/min
madobar group (5.76±1.23)lap/min and model group. ②Madobar and high dosage group compare to model group have increasing activity of substantia nigra (P<0.05)
as well as GSH-Px (P<0.01). Meanwhile
high dosage of BSHXF and madobar have similar increase in SOD
GSH-Px and decrease in MDA. ③TH immunohistochemistry result shows BSHXF high dosage and madobar group rat substantia nigra TH have large number of positive neuron
large soma size
significant outgrowth
the comparison of the two groups shows no statistical difference. PD model group has significant decrease in the number of neuron (P<0.01)
even disappearing
neuron soma atrophy
little outgrowth. Conclusion: There are protective effects of BSHXF on 6-OHDA type of Parkinson's disease in substantia nigra of rat dopaminergic neurons
its effect mechanism could achieved through anti-oxidative stress and increase level of tyrosine hydroxylase in substantia nigra.