ABSTRACT
Aim To investigate the protective effect of Banqiao Codonopsis pilosula (BCP) on cognitive function in rats with Alzheimer's disease(AD) induced by Okadaic acid (OA) and its possible mechanism. Methods SD rats were randomly divided into DMSO group, OA group and BCP low, medium, high treatment group. The rats were gavage administered in groups of one week and two weeks. The water maze training was continued for five days before modeling, and modeling was started 24 hours after the training. The bilateral hippocampus of DMSO group was injected with 10% DMSO 1.5 |xL. OA group and BCP treatment group were injected with OA (0. 392 mmol • L"1) 1.5 (iL. The water maze test was used to observe the spatial learning ability of rats. Western blot was used to observe the activity of PP2A, the phosphoryla-tion of Tau protein and the expression of synaptic protein in hippocampus, and the Nissl's staining to observe the changes of Nissl bodies in hippocampus CA1 and CA3. Results Water maze experiments showed that BCP could improve spatial memory impairment in AD rats. Western blot results showed that BCP in-creased PP2A activity, increased synaptic protein expression, and decreased Tau protein phosphorylation. Nissl's staining suggested an increase in the number of Nissl bodies in BCP treatment group. Conclusions BCP can up-regulate PP2A activity, decrease the phosphorylation level of Tau protein, increase the expression of synaptic proteins, and repair damaged neurons.
ABSTRACT
Aim To investigate the effect of astragalo- side Ⅳ on focal cerebral ischemia-reperfusion injury in rats.Methods The focal cerebral ischemia/reper-fusion of rat left middle cerebral artery occlusion ( MCAO) was induced by suture method .Male SD rats were randomly divided into sham operation group , cer-ebral ischemia/reperfusion group , astragaloside IV group and solvent control group .Except for the sham operation group , the others were subjected to ischemia 2h and reperfusion 24h.Then, rats with successful model were chosen for the detection of various indexes . Astragaloside IV group was injected intraperitoneally with astragaloside IV(20 mg· kg -1 ) at the same time as reperfusion , while solvent control group was injected with the same amount of solvent .TTC staining was used to detect the volume of cerebral infarction , and Nissl staining to observe the changes of histomorpholo-gy, and transmission electron microscope (TEM) to ob-serve the ultrastructure of the cells .Results There was no neurological deficit in the sham operation group, and the volume of cerebral infarction was zero . Compared with the sham operation group , there were some increased neurological deficits , nerve cell damage and cerebral infarction volume in other groups ( P <0.05) .Compared with the cerebral ischemia/reperfu-sion group , the nerve function damage could be signifi-cantly improved , the damage of neurons reduced , and the volume of cerebral infarction decreased ( P<0.05 ) in astragaloside IV group , and there was no obvious change in the solvent control group ( P>0.05 ) .Con-clusion Astragaloside IV can reduce the focal ische-mia/reperfusion injury in rats and protect nerve cells from damage.