Chun-lin MA, Hong-yan WU, Yong-qiang DUAN, et al. Effect of Hei Xiaoyaosan on Expression of CaMKⅡα Protein and Its Phosphorylation in Hippocampus and Cerebral Cortex of APP/PS1 Double Transgenic Mice[J]. Chinese journal of experimental traditional medical formulae, 2020, 26(6): 25-31.
DOI:
Chun-lin MA, Hong-yan WU, Yong-qiang DUAN, et al. Effect of Hei Xiaoyaosan on Expression of CaMKⅡα Protein and Its Phosphorylation in Hippocampus and Cerebral Cortex of APP/PS1 Double Transgenic Mice[J]. Chinese journal of experimental traditional medical formulae, 2020, 26(6): 25-31. DOI: 10.13422/j.cnki.syfjx.20200640.
Effect of Hei Xiaoyaosan on Expression of CaMKⅡα Protein and Its Phosphorylation in Hippocampus and Cerebral Cortex of APP/PS1 Double Transgenic Mice
To study the effect of Hei Xiaoyaosan on the expression of calcium calmodulin-dependent protein kinase Ⅱ alpha(CaMKⅡ
α
) and its phosphorylation in hippocampus and cortex of mice with Alzheimer's disease.
Method:
2
After weighing
30 APP/PSI transgenic male mice were divided into model group
donepezil hydrochloride group and Hei Xiaoyaosan group according to random principle and 10 in each group.At the same age
wild-type C57BL/6 10 mice of the same species were treated as blank group. Donepezil hydrochloride group (6 g·kg
-1
) and Hei Xiaoyaosan group (3.25 mg·kg
-1
) were administered for 90 days
then the behavior of all the mice were detected by Morris water maze
the expression of CaMKⅡ
α
p-CaMKⅡ
α
proteins in hippocampus and cortex by immunohistochemical technique and Western blot.
Result:
2
After intervention 3 months
compared with blank group
the average escaping latency periods prolonged significantly and the number of cross-platform and effective areas were decreased distinctly in model group mice(
P
<
0.01)
CaMKⅡ
α
protein relative expression decreased significantly(
P
<
0.01)
p-CaMKⅡ
α
protein relative expression increased significantly(
P
<
0.01). Compared with the model group
the escape latency of donepezil hydrochloride and Hei Xiaoyaosan group were significantly shortened
and the number of crossing platforms and effective areas was significantly increased (
P
<
0.05
P
<
0.01)
the expression of CaMKⅡ
α
protein in the hippocampus and cortex of drug groups was significantly increased (
P
<
0.01)
p-CaMKⅡ
α
protein in the hippocampus and cortex of drug groups was significantly decreased (
P
<
0.05
P
<
0.01).
Conclusion:
2
Hei Xiaoyaosan can improve the learning and memory ability of AD mice by regulating the expression of CaMKⅡ
α
and its phosphorylation
which are key proteins involved in the mechanism of cell memory formation in different brain regions of AD mice.
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