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Saponins In Polygala Enhance Synaptic Plasticity In Alzheimer’s Disease Rats Model

Posted on:2013-11-15Degree:MasterType:Thesis
Country:ChinaCandidate:S S ChenFull Text:PDF
GTID:2234330371478837Subject:Neurology
Abstract/Summary:PDF Full Text Request
0bjective①To observe the effects of Saponins in Polygala on the vivo hippocampallong-term potentiation of Alzheimer’s disease(AD) model rats, and to prove whether the effectswere dose-dependent.②To observe the effects of Saponins in Polygala on the hippocampalexpression level of NR2A in AD model rats.Methods 32 healthy male Wistar rats were randomly divided into four groups: control group,AD model group, low dose Saponins of Polygala group(12.5 mg/mL),high dose Saponins ofPolygala group(37.5 mg/mL). AD model rats were made by injecting ibotenic acid(IBO) intothe basal forebrain Meynert nuoleus of aged rats induced by D-gal. Using Electrophysiologicaltechnique LTP was determined by comparing the average field exciatatory postsynapticpotentia(fEPSP) amplitude after high frequency stimulation(HFS) with that of baseline period.The expression level of NR2A in the hippocampal CA1region was measured byImmunohistochemical technique.Results:1. The effects of Saponins in Polygala on the vivo hippocampal long-term potentiation ofAlzheimer’s disease(AD) model rats:After the HFS 1 minute, 30 minutes, and 60 minutes,thefEPSP amplitude of the control group respectively reached 203.17±7.47%, 178.15±8.11% and164.17±7.03%, while the model group fEPSP amplitude was significantly lower than the controlgroup( p<0.05), only respectively reached 173.63±10.81%, 127.12±7.38% and 102.88±2.36%.The fEPSP amplitude of high dose Saponins in polygalae group respectively reached192.00±2.45%, 168.00±2.45% and 141.75±9.25%, which were higher (p<0.05) than the lowdose group’s 177.67±14.04%, 131.83±4.96% and 121.17±4.79%. Compared with the modelgroup both of high and low dose group’s fEPSP amplitude were obviously improved (p<0.05).2. The effects of Saponins in Polygala on the hippocampal expression level of NR2A in ADmodel rats: The integral optical density values of control group, AD model group, low dosegroup and high dose group were respectly 30.12±3.45、11.74±1.69、20.78±2.66、25.86±2.98 .Compared with control group,the pyramidal cell layers in CA1of AD models becameindiscriminate, sparse and the expression of NR2A in the AD modle group was obivously less(p<0.05). Compared with model group, the expression of NR2A was significantly more in bothhigh dose group and low dose group(p<0.05, p<0.05). Furthermore, the expression of NR2A wassignificantly more in high dose group than low dose group (p<0.05).Conclusion: Saponins in polygala can significantly reduce the restraint to LTP induced byibotenic acid, and increase the expression of NR2A in the CA1region of AD model rats, and improve the synaptic plasticity dose-dependently.
Keywords/Search Tags:Saponins in polygala, Alzheimer’s disease, Synaptic plasticity, long-termpotentiation, N-methyl-D-aspartate receptor 2A subunit
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