血管性痴呆
PI3K/AKT/mTOR通路
蛋白激酶B
医学
海马体
缺血
海马结构
药理学
痴呆
信号转导
神经科学
内科学
生物
细胞生物学
疾病
作者
Xian Liu,Liwei Yao,Xinyi Ye,Yufeng Qin,Shuyun Chen,Qiyao Jiang,Meng Liu,Xiaotong Chen,Weirong Li,Chaozhan Lin,Chenchen Zhu,Wei Zhao,Qi Wang
标识
DOI:10.1016/j.brainres.2024.149135
摘要
Vascular dementia (VD) is a disease characterized by cognitive impairment and memory loss due to brain cell damage caused by cerebral vascular ischemia. Danggui-Shaoyao-San (DSS) has been used clinically to treat diseases for centuries. The VD model was established by bilateral common carotid artery (BCCA) repeated ischemia-reperfusion (I/R) and caudal bleeding. Target prediction of DSS and miR-124 in PI3K/Akt signaling pathway by network pharmacology. The effect of DSS on cognitive dysfunction were evaluated through methods such as behavioral experiments, cerebral blood flow monitoring, HE and Nissl staining, western blot, and q-PCR. Prediction result showed that both DSS and miR-124 could target Akt1. DSS treatment significantly reduced hippocampal cell damage, improved learning and memory ability. Mechanically, DSS treatment up-regulated the expression levels of PI3K and Akt protein, and its gene. Bcl-2/Bax index is up-regulated and cell apoptosis reduced. LC3II/LC3I index decreased and autophagy of brain cells increased. Moreover, DSS down-regulated the expression level of miR-124. And inhibition of miR-124 up-regulate the expression of PI3K, Akt. These results suggested that DSS can reduce the content of miR-124 in the hippocampus of VD mice, thus regulating the PI3K/Akt signaling pathway and improving the learning and memory ability of VD mice.
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