Therapeutic potential of Shilong Qingxue Granule and its extract against glutamate induced neural injury: Insights from in vivo and in vitro models

被引:0
|
作者
Hu, Nan [1 ,2 ]
Zeng, Cheng [1 ]
Cao, Yi [1 ]
Li, Xuehao [1 ]
Bai, Fei [2 ,3 ]
Wang, Jinhui [3 ]
Yang, Baofeng [1 ,3 ]
Li, Chunli [1 ,2 ]
机构
[1] Shenyang Pharmaceut Univ, Dept Pharmacol, Shenyang, Liaoning, Peoples R China
[2] Shenzhen Technol Univ, Coll Pharm, Shenzhen, Guangdong, Peoples R China
[3] Harbin Med Univ, Dept Pharm, Harbin 150081, Heilongjiang, Peoples R China
关键词
Shilong Qingxue Granule; Glutamate; Apoptosis; MAPKs; INDUCED APOPTOSIS; BRAIN; CELLS; NEUROTRANSMITTER; EXCITOTOXICITY; RELEASE;
D O I
10.1016/j.jep.2025.119396
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Shilong Qingxue Granule (SQG), a traditional Chinese medicine, effectively treats the secondary neurological damage and functional deficits caused by cerebral hemorrhage, though its exact mechanism remains unclear. Aim of the study: This study aimed to investigate the effects of SQG and its mechanisms. Materials and methods: we evaluated the effects of SQG and its extracts on glutamate induced nerve damage using in vivo and in vitro models. Brain water content was measured and brain tissue was stained with hematoxylin and eosin (HE) to evaluate the brain protective effect of SQG in rats. HPLC and UPLC-Q-TOF-MS were used to identify the chemical components in SQG. The model of PC12 cells induced by glutamate was established to detect intracellular Ca2+ and mitochondrial membrane potential (MMP), the content of intracellular reactive oxygen species (ROS), acridine orange/ethidium bromide (AO/EB), and the possible mechanism of action in vivo was explored by Western blot and RNA sequencing. Results: SQG alleviates brain edema and neuronal damage in glutamate induced rats by modulating mitochondrial apoptotic and MAPK signaling pathways. The SQG extract was separated by silica gel chromatographic column to obtain 20 components, and the S-18 improves PC12 survival under glutamate induced conditions by MMP, reducing ROS and Ca2+ levels, and protecting against cell body and nucleus damage to against apoptosis. Conclusion: SQG and its extract demonstrate protective effects against glutamate induced nerve injury in vivo and in vitro, suggesting potential therapeutic benefits for neurological disorders involving glutamate excitotoxicity.
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页数:11
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