Dihuang Yinzi improves scopolamine-induced learning and memory impairment by regulating plasma exosome-derived BDNF

被引:0
|
作者
Su, Wenna [1 ,2 ,3 ]
Du, Yuzhong [2 ,3 ,4 ]
Wang, Wenting [1 ,2 ,3 ]
Li, Qinqing [1 ,2 ,3 ]
Zhang, Junlong [1 ,2 ,3 ]
He, Wenbin [1 ,2 ,3 ]
机构
[1] Shanxi Univ Chinese Med, Sch Basic Med Sci, Jinzhong 030619, Shanxi, Peoples R China
[2] Shanxi Prov Key Lab Chinese Med Encephalopathy, Jinzhong, Peoples R China
[3] Natl Int Joint Res Ctr Mol Chinese Med, Jinzhong, Peoples R China
[4] Shanxi Med Univ, Jinzhong 030619, Shanxi, Peoples R China
关键词
Dihuang yinzi; Alzheimer's disease; Exosomes; Synaptic plasticity; Cholinergic system; EXTRACELLULAR VESICLES; NEUROTROPHIC FACTOR; COGNITIVE DEFICITS; BRAIN; MAINTENANCE; HYPOTHESIS;
D O I
10.1016/j.jep.2025.119322
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Dihuang Drink (DHD), formulated by Liu Hejian during the Yuan Dynasty, is listed as one of the first ancient classical prescriptions by the National Medical Products Administration of China. It is commonly used for the prevention and treatment of Alzheimer's disease (AD). This study further investigates the therapeutic effects and potential mechanisms of DHD in AD. Aim of the study: This study aimed to evaluate the cognitive improvement effects of DHD on scopolamine (SCOP)induced memory impairment in mice and to explore its anti-AD mechanisms mediated by exosomes. Materials and methods: A cognitive impairment model was established in C57BL/6J mice via intraperitoneal injection of SCOP (1 mg/kg) for 21 consecutive days, followed by DHD intervention to assess its effects on learning, memory, hippocampal synaptic density, and the cholinergic system. SD rats were gavaged with DHD (22.00 g/kg) for 7 days, and plasma exosomes were extracted. These exosomes were injected into SCOP-treated mice (2 mg/kg, every other day for 14 days, 7 injections) to verify the role of exosomes in improving cognitive function. Behavioral performance and brain ChAT and BDNF levels were measured. Results: DHD improved learning and memory in SCOP model mice, attenuated neuronal loss and decreases in dendritic spines induced by scopolamine, and modulated the expression of BDNF, SYN-1, PSD95, and M1 mAChR. DHD-derived plasma exosomes further enhanced learning and memory function and significantly increased brain ChAT activity and BDNF levels. Conclusions: DHD may alleviate cognitive impairment in SCOP model mice, potentially through exosomemediated neuroprotection.
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页数:16
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