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基于代谢组学研究对乙酰氨基酚片对中国健康成人胆汁酸谱的影响

Metabolomics-based analysis of serum BAs in healthy Chinese adults taking acetaminophen

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【作者】 杨倩俞蕴莉张全英

【Author】 YANG Qian;YU Yunli;ZHANG Quanying;Soochow University;Department of Oncology,the Second Affiliated Hospital of Soochow University;

【通讯作者】 张全英;

【机构】 苏州大学苏州大学附属第二医院临床药理实验室

【摘要】 目的:研究健康成人多次口服对乙酰氨基酚片后胆汁酸代谢的变化。方法:招募10名健康受试者,收集受试者口服对乙酰氨基酚前后的血清标本,分为给药前组(PD),第5次给药后组(FD)及第8次给药后组(ED),采用高效液相串联质谱(LC-MS/MS)的方法,定量检测血清胆汁酸谱,并结合代谢组学的主成分分析(PCA),正交偏最小二乘法判别分析(OPLS-DA),研究多次口服对乙酰氨基酚后健康成人胆汁酸代谢谱的变化,检测各组肝功能生化指标,观察在给药前后肝功能生化指标的变化。结果:在给药前和给药后人血清的胆汁酸谱发生了变化,牛磺鹅去氧胆酸(TCDCA),甘氨胆酸(GCA),甘氨鹅脱氧胆酸(GCDCA),牛磺熊去氧胆酸(TUDCA)的浓度与给药前的基线相比显著升高(P<0.05),肝功能生化指标无明显的变化。采用代谢组学的方法筛选出的差异代谢物GCA,GCDCA为口服对乙酰氨基酚后胆汁酸改变最敏感的指标。结论:GCA和GCDCA或可作为对乙酰氨基酚致早期肝损伤的潜在生物标志物。

【Abstract】 AIM: To investigate the changes of bile acid metabolism in healthy adults after taking acetaminophen. METHODS: Ten healthy subjects were enrolled and the serum samples of subjects before and after multiple administration of acetaminophen were collected. They were divided into pre-dose group (PD),fifth-dose gro-up (FD) and eighth-dose group (ED). A high performance liquid chromatographytandem mass spectrometric method (HPLC-MS/MS)was used to quantify 15 target-edbile acid metabolites in human plasma,combined with principal component analysis (PCA),orthogonal partial least squares discriminant analysis (OPLS-DA) to investigate the changes of bile acid metabolism profile in healthy adults after taking acetaminophen. And the biochemical indicators of each group were detected. RESULTS: There was a change in the bile acid spectrum of human serum after taking acetaminophen. Compared with group PD,the taurochenodeoxycholicacid (TCDCA),glycocholicacid (GCA),glycochenodeoxycholic acid (GCDCA) and tauroursodeoxycholic acid (TUDCA) levels were significantly increased (P<0. 05). There was no obvious changes in biochemical indicators. GCA and GCDCA were the most sensitive indicators of bile acid. CONCLUSION: GCA and GCDCA can be used as potential biomarkers of early liver injury caused by acetaminophen.

【基金】 国家自然科学基金(81603181)
  • 【文献出处】 中国临床药理学与治疗学 ,Chinese Journal of Clinical Pharmacology and Therapeutics , 编辑部邮箱 ,2021年03期
  • 【分类号】R969
  • 【被引频次】1
  • 【下载频次】298
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