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作 者:周倩 刘奎 马静 谭光国 ZHOU Qian;LIU Kui;MA Jing;TAN Guangguo(Department of Traditional Chinese Medicine,Xijing Hospital,Air Force Medical University;Cadets Brigade,Basic Medicine College,Air Force Medical Universit;Department of Pharmaceutical Analysis,School of Pharmacy,Air Force Medical University,Xi'an 710032,China)
机构地区:[1]空军军医大学第一附属西京医院中医科,陕西西安710032 [2]空军军医大学基础医学院学员一旅,陕西西安710032 [3]空军军医大学药学系药物分析学教研室,陕西西安710032
出 处:《药学实践杂志》2018年第4期313-317,共5页Journal of Pharmaceutical Practice
基 金:国家自然科学基金项目(81773677;81402888)
摘 要:目的采用基于气相色谱-质谱(GC-MS)血清代谢组学技术研究芪附汤抗阿霉素心脏毒性的作用,并初步探讨其作用机制。方法将24只大鼠分为正常组、阿霉素组和芪附汤治疗组,给予4周相应的干预治疗后,采集大鼠血清进行GC-MS分析,结合多变量和单变量统计分析,研究阿霉素诱导的心脏毒性损伤大鼠血清中内源性代谢物的变化,以及芪附汤对其的干预作用,寻找其抗阿霉素心脏毒性潜在的生物标志物,采用代谢通路分析鉴定芪附汤靶向代谢通路。结果 GC-MS血清代谢组学分析鉴定了17种阿霉素心脏毒性潜在生物标志物,芪附汤对其中10种代谢物具有显著的逆转作用,代谢通路分析表明,三羧酸循环、乙醛酸和二羧酸代谢(简称二羧酸代谢)、花生四烯酸代谢是芪附汤主要的靶向代谢通路。结论芪附汤能够通过调节失衡的三羧酸循环、二羧酸代谢和花生四烯酸代谢而发挥抗阿霉素心脏毒性的作用。Objective To evaluate the protective effect of Qifu decoction(QFD)on adriamycin-induced cardiac injury based on GC-MS serum metabolomics and explore its mechanism.Methods Twenty-four rats were randomly divided into three groups:control group,Adriamycin-induced model group and QFD-treated group.The QFD-treated group received QFD for 4 weeks.After 4 weeks,the serum samples of each rat were collected and analyzed by GC-MS.Combination GC-MS with multivariate and univariate statistical analysis was applied to identify potential biomarkers related with adriamycin-induced cardiac injury and QFD-reversed biomarkers.Metabolic pathway analysis was employed to identify QFD-targeted metabolic pathways.Results 17 metabolites were identified as potential biomarkers related with adriamycin-induced cardiac injury based on GC-MS serum metabolomics analysis and 10 metabolites were significantly reversed by QFD.QFD-targeted metabolic pathways were identified by metabolic pathway analysis with MetaboAnalyst,which were citrate cycle,glyoxylate and dicarboxylate metabolism and arachidonic acid metabolism.Conclusion QFD administration provided protective effects on adriamycin-induced cardiac injury through partially regulating the perturbed citrate cycle,glyoxylate and dicarboxylate metabolism and arachidonic acid metabolism.
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