银杏黄酮苷元减轻多柔比星心脏毒性的作用机制 点击下载
| 论文标题： | 银杏黄酮苷元减轻多柔比星心脏毒性的作用机制 |
| 英文标题： | |
| 中文摘要： | 目的 探究银杏黄酮苷元（GA）减轻多柔比星（DOX）心脏毒性的潜在作用机制。方法将雄性ICR小鼠随机分为对照组（CON组）、模型组（DOX组）和GA+DOX组（GDOX组），每组12只。DOX组小鼠隔天尾静脉注射DOX药液3mg/kg，GDOX组小鼠每天灌胃GA混悬液100mg/kg+隔天尾静脉注射DOX药液3mg/kg，连续15d。给药结束后，检测各组小鼠血清中天冬氨酸转氨酶（AST）、肌酸激酶（CK）、肌酸激酶同工酶（CK-MB）、乳酸脱氢酶（LDH）水平。基于代谢组学方法，采用超高效液相色谱-四极杆静电场轨道阱串联质谱技术，在主成分分析（PCA）、正交偏最小二乘-判别分析（OPLS-DA）的基础上，以变量重要性投影值≥1、峰面积差异倍数＞1且P＜0.05为标准筛选差异代谢物（DEMs），并基于HMDB、PubChem等数据库进行生物学分析。结果与CON组比较，DOX组小鼠血清中AST、CK、CK-MB、LDH水平均显著升高（P＜0.05）；与DOX组比较，GDOX组小鼠血清中上述指标（CK-MB除外）水平均显著降低（P＜0.05）。PCA、OPLS-DA结果均显示，CON组、DOX组、GDOX组小鼠心脏组织样品均能完全分离。经数据库匹配后，鉴定出37个共有DEMs，其中DOX组显著上调而GDOX组显著下调的DEMs有17个，DOX组显著下调而GDOX组显著上调的DEMs有8个；涉及通路包括不饱和脂肪酸的生物合成、花生四烯酸代谢、亚油酸代谢、牛磺酸和次牛磺酸代谢，关键代谢物包括二十二碳六烯酸、花生四烯酸、磷脂酰胆碱（16∶0/18∶3）和牛磺酸。结论GA可能通过作用于二十二碳六烯酸、花生四烯酸等关键代谢物来调节不饱和脂肪酸的生物合成、花生四烯酸代谢等代谢途径，进而减轻DOX的心脏毒性。 |
| 英文摘要： | OBJECTIVE To investigate the potential mechanism of the effect of ginkgo flavone aglycone （GA） against doxorubicin （DOX）-induced cardiotoxicity. METHODS The male ICR mice were randomized into control group （CON group）， model group （DOX group） and GA+DOX group （GDOX group）， with 12 mice in each group. The DOX group was injected with DOX solution at a dose of 3 mg/kg via tail vein every other day， and the GDOX group was given GA suspension intragastrically at a dose of 100 mg/kg every day+DOX solution at a dose of 3 mg/kg via tail vein every other day， for 15 consecutive days. After the end of administration， the serum levels of aspartate aminotransferase（AST）， creatine kinase（CK）， creatine kinase isoenzyme（CK- MB） and lactate dehydrogenase（LDH） in mice were detected in each group. Based on the metabolomics method， UHPLC-Q- Exactive Orbitrap HRMS method was used； based on principal component analysis （PCA） and orthogonal partial least squares- discriminant analysis （OPLS-DA）， the differentially expressed metabolites （DEMs） were screened using the criteria of variable importance in the projection≥1， fold change of peak area＞1 and P＜0.05； biological analysis was conducted based on databases such as HMDB and PubChem. RESULTS Compared with CON group， serum levels of AST， CK， CK-MB and LDH were increased significantly in DOX group （P＜0.05）； compared with DOX group， the serum levels of the above indicators （except for CK-MB） were decreased significantly in GDOX group （P＜0.05）. PCA and OPLS-DA showed that myocardial tissue samples of CON group， DOX group and GDOX group were isolated completely. After database matching， 37 common DEMs were identified， among which 17 DEMs were significantly up-regulated in the DOX group and significantly down- regulated in the GDOX group， and 8 DEMs were significantly down-regulated in the DOX group and significantly up-regulated in the GDOX group； pathway enrichment involved the biosynthesis of unsaturated fatty acids， arachidonic acid metabolism， linoleic acid metabolism， taurine and hypotaurine metabolism； the key metabolites in the above pathways included docosahexaenoic acid， arachidonic acid， phosphatidylcholine （16∶0/18∶3） and taurine. CONCLUSIONS GA may regulate the biosynthesis of unsaturated fatty acids， arachidonic acid metabolism and other metabolic pathways by acting on the core metabolites such as docosahexaenoic acid and arachidonic acid， thus alleviating the cardiotoxic effects of DOX. |
| 期刊： | 2024年第35卷第06期 |
| 作者： | 蔡英；钱丽；王开靓；李琴；刘春花；孙佳；潘洁；李勇军；陆苑 |
| 英文作者： | CAI Ying，QIAN Li，WANG Kailiang，LI Qin，LIU Chunhua，SUN Jia，PAN Jie，LI Yongjun，LU Yuan |
| 关键字： | 银杏黄酮苷元；多柔比星；心脏毒性；代谢组学 |
| KEYWORDS： | ginkgo flavonoid aglycone； doxorubicin； cardiotoxicity； metabolomics |
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