The effect of Scutellaria baicalensis stem-leaf flavonoids on spatial learning and memory in chronic cerebral ischemia-induced vascular dementia of rats

被引:22
作者
Cao, Yanjing [1 ,2 ]
Liang, Lizhen [2 ]
Xu, Jian [3 ]
Wu, Jiali [2 ]
Yan, Yongxing [2 ]
Lin, Ping [2 ]
Chen, Qiang [2 ]
Zheng, Fengming [2 ]
Wang, Qin [2 ]
Ren, Qian [2 ]
Gou, Zengmei [4 ]
Du, Yifeng [1 ]
机构
[1] Shandong Univ, Shandong Prov Hosp, Dept Neurol, Jinan 250013, Peoples R China
[2] Third Hosp Hangzhou, Dept Neurol, Hangzhou 310009, Zhejiang, Peoples R China
[3] Zhejiang Chinese Med Univ, Dept Histol & Embryol, Hangzhou 310053, Zhejiang, Peoples R China
[4] Second Peoples Hosp Weifang, Dept Neurol, Weifang 261041, Peoples R China
关键词
flavonoid; vascular dementia; deficits of spatial learning and memory; hyperphosphorylated tau; CYCLIN-DEPENDENT KINASE-5; TRANSGENIC MOUSE MODEL; ALZHEIMERS-DISEASE; COGNITIVE IMPAIRMENT; ISCHEMIA/REPERFUSION INJURY; PHOSPHATASE-ACTIVITY; NEURONAL DAMAGE; BRAIN; TAU; NEURODEGENERATION;
D O I
10.1093/abbs/gmw024
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Flavonoids have been shown to improve cognitive function and delay the dementia progression. However, the underlying mechanisms remain elusive. In the present study, we examined the effect of Scutellaria baicalensis stem-leaf total flavonoids (SSTFs) extracted from S. baicalensis Georgi on spatial learning and memory in a vascular dementia (VaD) rat model and explored its molecular mechanisms. The VaD rats were developed by permanent bilateral occlusion of the common carotid artery. Seven days after recovery, the VaD rats were treated with either 50 or 100 mg/kg of SSTF for 60 days. The spatial learning and memory was evaluated in the Morris water maze (MWM) test. The tau hyperphosphorylation and the levels of the related protein kinases or phosphatases were examined by western blot analysis. In VaD rats, SSTF treatment at 100 mg/kg significantly reduced the escape latency in training trial in MWM test. In the probe trial, SSTF treatment increased the searching time and travel distance in the target quadrant. SSTF treatment inhibited the tau phosphorylation in both cortex and hippocampus in VaD rats. Meanwhile, SSTF reduced the activity of glycogen synthase kinase 3 beta and cyclin-dependent kinase 5 in VaD rats. In contrast, SSTF treatment increased the level of the protein phosphatase 2A subunit B in VaD rats. SSTF treatment significantly improved the spatial cognition in VaD rats. Our results suggest that SSTF may alleviate tauhyperphosphorylation-induced neurotoxicity through coordinating the activity of kinases and phosphatase after a stroke. SSTF may be developed into promising novel therapeutics for VaD.
引用
收藏
页码:437 / 446
页数:10
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