秋水仙碱
代谢组学
化学
药理学
代谢途径
精氨酸
轨道轨道
生物化学
新陈代谢
内科学
氨基酸
色谱法
医学
质谱法
作者
Wei Wen,Zhongxiao Zhang,Bing Jiang,Ying Hao
摘要
Abstract Myocardial infarction (MI) is one of the most common causes of death worldwide. A metabolomic approach based on an ultra‐high performance liquid chromatography–Orbitrap analytical method was established to analyze the metabolites and to investigate the therapeutic mechanism of colchicine. Forty‐six biomarkers were significantly changed between the sham group and the MI group. Thirty‐five metabolites were increased and 11 were decreased in MI rats, and colchicine reversed all of them. Pathway analysis showed that the TCA cycle, alanine, aspartate and glutamate metabolism, glycerophospholipid metabolism, aminoacyl‐tRNA biosynthesis, glyoxylate and dicarboxylate metabolism and arginine biosynthesis were altered in the MI group. Ingenuity pathway function and network analysis showed that colchicine improved MI through regulation of cardiac β ‐adrenergic signaling and cardiac hypertrophy signaling. The present study provided a useful approach for exploring the mechanism of MI and evaluating the efficacy of colchicine.
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