脑梗死脂质代谢基因鉴定及活血荣络方的干预作用OACSTPCD
Identification of Lipid Metabolism Genes in Cerebral Infarction and Intervention Effect of Huoxue Rongluo Prescription
目的 鉴定脑梗死脂质代谢基因,并探讨活血荣络方的干预作用.方法 采用多芯片联合差异分析(GSE61616、GSE30655),结合Reactome数据库,鉴定出脑梗死脂质代谢基因,并在GSE97537芯片中鉴定并验证脑梗死脂质代谢基因的表达差异;采用Pearson相关性分析GSE61616、GSE30655、GSE97537、GSE137595、GSE22255、GSE163614、GSE78731 数据集中 51 个脑梗死样本mRNA表达相关性;通过STRING数据库、R语言clusterProfiler包对脑梗死脂质代谢基因进行蛋白相互作用及GO、KEGG富集分析.制备脑梗死模型大鼠,并予活血荣络方浸膏11.7 g/kg灌胃给药,连续7 d,观察大鼠神经功能缺损症状、Nissl小体变化及脑梗死脂质代谢关键基因PLA2G4A、SPHK1、PTGS1 mRNA表达.结果 TSPO、CYP1B1、PLIN2、CH25H、PLA2G4A、ANGPTL4、PTGS1、SPHK1、PTGES被鉴定为脑梗死脂质代谢基因,在脑梗死中显著高表达且显著正相关,其中PTGS1、PLA2G4A、SPHK1相互作用关系最强,是脑梗死脂质代谢关键基因;脑梗死脂质代谢基因主要发挥氧化还原酶活性、铁离子结合、血红素结合等分子功能,介导花生四烯酸代谢、磷脂酶D信号通路、VEGF信号通路,参与脂质代谢调控进程、脂肪酸代谢进程、脂肪酸衍生物代谢过程.脑梗死模型大鼠神经功能缺损症状严重(P<0.001),活血荣络方能有效改善模型大鼠神经功能缺损(P<0.001);Nissl染色结果提示,脑梗死后神经元结构异常,数目明显减少(P<0.001),活血荣络方能增加神经元数目(P<0.001),修复神经元结构;RT-qPCR结果提示,脑梗死脂质代谢关键基因在脑梗死中显著高表达(P<0.001),与生物信息学结果一致,活血荣络方能降低脂质代谢关键基因PTGS1、PLA2G4A、SPHK1表达(P<0.001,P<0.01,P<0.05).结论 活血荣络方能下调PTGS1、PLA2G4A、SPHK1表达,发挥氧化还原酶活性、铁离子结合、血红素结合等分子功能,介导花生四烯酸代谢、磷脂酶D信号通路、VEGF信号通路,参与脂质代谢调控进程、脂肪酸代谢进程、脂肪酸衍生物代谢过程,增加Nissl小体数目,改善神经功能缺损症状,发挥神经保护作用.
Objective To identify lipid metabolism genes in cerebral infarction;To explore the intervention effect of Huoxue Rongluo Prescription.Methods Multi-chip combined differential analysis(GSE61616,GSE30655)was used to identify lipid metabolism genes in cerebral infarction in combination with Reactome database,and the expression differences of lipid metabolism genes in cerebral infarction were identified and verified in GSE97537 chip;Pearson correlation analysis was used to analyze the correlation of 51 cerebral infarction samples in GSE61616,GSE30655,GSE97537,GSE137595,GSE22255,GSE163614,and GSE78731 datasets;PPI,GO and KEGG analysis of lipid metabolism genes in cerebral infarction were performed through STRING database and R clusterProfiler package.SD rats were made to the model of cerebral infarction,and was administered with Huoxue Rongluo Prescription extract 11.7 g/kg by intragastric administration for 7 days.The symptoms of neurological deficit,the changes of Nissl bodies and the mRNA expressions of PLA2G4A,SPHK1,and PTGES key genes in lipid metabolism in cerebral infarction were observed.Results TSPO,CYP1B1,PLIN2,CH25H,PLA2G4A,ANGPTL4,PTGS1,SPHK1,and PTGES were identified as lipid metabolism genes in cerebral infarction,and were significantly highly expressed and positively correlated in cerebral infarction.Among them,PTGS1,PLA2G4A,and SPHK1 interacted with each other,which were the key genes of lipid metabolism in cerebral infarction;the lipid metabolism gene in cerebral infarction mainly exerted molecular functions such as oxidoreductase activity,iron ion binding,heme binding,etc.,mediating arachidonic acid metabolism,phospholipase D signaling pathway,VEGF signaling pathway,involved in regulation of lipid metabolism process,fatty acid metabolism process,fatty acid derivative metabolism process.The symptoms of neurological deficit in the model rats with cerebral infarction were severe(P<0.001),and Huoxue Rongluo Prescription could effectively improve the neurological deficit of model rats(P<0.001).The Nissl staining indicated that the neuronal structure was abnormal and the number was significantly reduced after cerebral infarction(P<0.001).Huoxue Rongluo Prescription could increase the number of neurons(P<0.001)and repair the neuronal structure.RT-qPCR showed that the key genes of lipid metabolism in cerebral infarction were significantly higher in cerebral infarction(P<0.001),corroborated with the bioinformatics results,and Huoxue Rongluo Prescription could reduce the expression of key lipid metabolism genes of PTGS1,PLA2G4A,and SPHK1(P<0.001,P<0.01,P<0.05).Conclusion Huoxue Rongluo Prescription can down-regulate the expressions of PTGS1,PLA2G4A,SPHK1,exert molecular functions such as oxidoreductase activity,iron ion binding,heme binding,and mediate arachidonic acid metabolism,phospholipase D signaling pathway,and VEGF signaling pathway.It participates in the process of lipid metabolism regulation,fatty acid metabolism,and fatty acid derivative metabolism,increases the number of Nissl bodies,improves the symptoms of neurological deficits,and exerts neuroprotective effects.
颜思阳;杨仁义;李飞亚;何孟豪;刘利娟;周德生;高晓峰
湖南中医药大学第一附属医院,湖南 长沙 410007湖南中医药大学,湖南 长沙 410007
中医学
脑梗死脂质代谢生物标志物实验验证大鼠
cerebral infarctionlipid metabolismbiomarkersexperimental validationrats
《中国中医药信息杂志》 2024 (002)
从星形胶质细胞足突离子网络调控机制探讨安脑平冲方对脑出血脑水肿的作用机理
33-40 / 8
国家自然科学基金(81874463、82104766);湖南省自然科学基金(2021JJ30521、2021JJ40424);湖南省教育厅科学研究项目(20C1405);湖南省卫生健康委科研计划项目(202103071190);中国卒中学会脑血管病全程管理项目-启航基金(CSA-SF-2021-03);湖南中医药大学校级科研基金(2021XJJJ052、2022XYLH016)
评论