Metabolomics Analysis of Electroacupuncture Pretreatment Induced Neuroprotection on Mice with Ischemic Stroke

神经保护 糖酵解 缺血 药理学 医学 脑缺血 冲程(发动机) 电针 代谢组学 新陈代谢 麻醉 内科学 针灸科 生物 生物信息学 病理 机械工程 工程类 替代医学
作者
Su-Hao Yang,Xin‐Xiao Zhang,Zhanqiong Zhong,Xia-Xia Luo,Yufei Wang,Xing-Ping Xiao,Ze-Qin Huang,Siyi Yu,Jiayi Sun,Meijun Liu,Xiao‐Yi Xiong
出处
期刊:The American Journal of Chinese Medicine [World Scientific]
卷期号:51 (05): 1127-1151 被引量:11
标识
DOI:10.1142/s0192415x23500520
摘要

The brain metabolic changes caused by the interruption of blood supply are the initial factors of brain injury in ischemic stroke. Electroacupuncture (EA) pretreatment has been shown to protect against ischemic stroke, but whether its neuroprotective mechanism involves metabolic regulation remains unclear. Based on our finding that EA pretreatment significantly alleviated ischemic brain injury in mice by reducing neuronal injury and death, we performed a gas chromatography-time of flight mass spectrometry (GC-TOF/MS) to investigate the metabolic changes in the ischemic brain and whether EA pretreatment influenced these changes. First, we found that some glycolytic metabolites in the normal brain tissues were reduced by EA pretreatment, which may lay the foundation of neuroprotection for EA pretreatment against ischemic stroke. Then, 6[Formula: see text]h of cerebral ischemia-induced brain metabolic changes, especially the enhanced glycolysis, were partially reversed by EA pretreatment, which was manifested by the brain levels of 11 of 35 up-regulated metabolites and 18 of 27 down-regulated metabolites caused by cerebral ischemia significantly decreasing and increasing, respectively, due to EA pretreatment. A further pathway analysis showed that these 11 and 18 markedly changed metabolites were mainly involved in starch and sucrose metabolism, purine metabolism, aspartate metabolism, and the citric acid cycle. Additionally, we found that EA pretreatment raised the levels of neuroprotective metabolites in both normal and ischemic brain tissues. In conclusion, our study revealed that EA pretreatment may attenuate the ischemic brain injury by inhibiting glycolysis and increasing the levels of some neuroprotective metabolites.
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