Li Long-Fei, Gao Ying, Xu Yuan, Su Dan-Jie, Yang Qi, Liu An, Wang Sai-Ying, Tang Xiu-Ling, Zhao Jun, Luo Li, Yan Tao, Wu Yu-Mei, Liu Shui-Bing, Zhao Ming-Gao, Yang Le
Precision Pharmacy & Drug Development Center, Department of Pharmacy, The Second Affiliated Hospital of Air Force Medical University, Xi'an, China.
Department of Pharmacology, School of Pharmacy, Air Force Medical University, Xi'an, China.
Phytother Res. 2023 Oct;37(10):4838-4850. doi: 10.1002/ptr.7949. Epub 2023 Jul 17.
Diabetic encephalopathy is a common consequence of diabetes mellitus that causes cognitive dysfunction and neuropsychiatric disorders. Praeruptorin C (Pra-C) from the traditional Chinese medicinal herb Peucedanum praeruptorum Dunn. is a potential antioxidant and neuroprotective agent. This study was conducted to investigate the molecular mechanisms underlying the effect of Pra-C on diabetic cognitive impairment. A novel object recognition test and the Morris water maze test were performed to assess the behavioral performance of mice. Electrophysiological recordings were made to monitor synaptic plasticity in the hippocampus. A protein-protein interaction network of putative Pra-C targets was constructed, and molecular docking simulations were performed to predict the potential mechanisms of the action of Pra-C. Protein expression levels were detected by western blotting. Pra-C administration significantly lowered body weight and fasting blood glucose levels and alleviated learning and memory deficits in type 2 diabetic mice. Network pharmacology and molecular docking results suggested that Pra-C affects the PI3K/AKT/GSK3β signaling pathway. Western blot analysis confirmed significant increases in phosphorylated PI3K, AKT, and GSK3β levels in vivo and in vitro upon Pra-C administration. Pra-C alleviated cognitive impairment in type 2 diabetic mice by activating PI3K/AKT/GSK3β pathway.
糖尿病性脑病是糖尿病的常见并发症,可导致认知功能障碍和神经精神疾病。来源于传统中药材白花前胡的白花前胡丙素(Pra-C)是一种潜在的抗氧化剂和神经保护剂。本研究旨在探讨Pra-C对糖尿病认知障碍影响的分子机制。采用新物体识别试验和莫里斯水迷宫试验评估小鼠的行为表现。进行电生理记录以监测海马体中的突触可塑性。构建了假定的Pra-C靶点的蛋白质-蛋白质相互作用网络,并进行分子对接模拟以预测Pra-C的潜在作用机制。通过蛋白质印迹法检测蛋白质表达水平。给予Pra-C可显著降低2型糖尿病小鼠的体重和空腹血糖水平,并减轻其学习和记忆缺陷。网络药理学和分子对接结果表明,Pra-C影响PI3K/AKT/GSK3β信号通路。蛋白质印迹分析证实,给予Pra-C后,体内和体外磷酸化PI3K、AKT和GSK3β水平均显著升高。Pra-C通过激活PI3K/AKT/GSK3β通路减轻2型糖尿病小鼠的认知障碍。