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Targeted bile acids metabolomics in cholesterol gallbladder polyps and gallstones: From analytical method development towards application to clinical samples

查看全文 作  者:Jiaojiao [1]Wei;Tao [2]Chen;Yamin [1]Liu;Shuai [1]Sun;Zhiqing [2]Yuan;Yixin [1]Zhang;Aizhen [1]Xiong;Linnan [1]Li;Zhengtao [1]Wang;Li [1]Yang 高影响力作者 机构地区:[1]The MOE Key Laboratory of Standardization of Chinese Medicines,The SATCM Key Laboratory of New Resources and Quality Evaluation of Chinese Medicines,The Shanghai Key Laboratory for Compound Chinese Medicines,Institute of Chinese Materia Medica,Shanghai University of Traditional Chinese Medicine,Shanghai 201203,China;[2]Department of Biliary and Pancreatic Surgery,Renji Hospital,School of Medicine,Shanghai Jiao Tong University,Shanghai,200127,China高影响力机构 出  处:《Journal of Pharmaceutical Analysis》索引2023年第13卷第9期,共8页高影响力期刊 基  金:supported by the National Natural Science Foundation of China(Grant Nos.:81920108033,and 82274223). 摘  要:Bile acids(BAs)are synthesized by the liver from cholesterol through several complementary pathways and aberrant cholesterol metabolism plays pivotal roles in the pathogeneses of cholesterol gallbladder polyps(CGP)and cholesterol gallstones(CGS).To date,there is neither systematic study on BAs profile of CGP or CGS,nor the relationship between them.To explore the metabolomics profile of plasma BAs in healthy volunteers,CGP and CGS patients,an ultra-performance liquid chromatography-tandem mass spectrometry(UPLC-MS/MS)method was developed and validated for simultaneous determination of 42 free and conjugated BAs in human plasma.The developed method was sensitive and reproducible to be applied for the quantification of BAs in the investigation of plasma samples.The results show that,compared to healthy volunteers,CGP and CGS were both characterized by the significant decrease in plasma BAs pool size,furthermore CGP and CGS shared aberrant BAs metabolic characteristics.Chenodeoxycholic acid,glycochenodeoxycholic acid,l-muricholic acid,deoxycholic acid,and 7-ketolithocholic acid were shared potential markers of these two cholesterol gallbladder diseases.Subsequent analysis showed that clinical characteristics including cysteine,ornithine and body mass index might be closely related to metabolisms of certain BA modules.This work provides metabolomic information for the study of gallbladder diseases and analytical methodologies for clinical target analysis and efficacy evaluation related to BAs in medical institutions. 关 键 词:Bile acid metabolism Gallbladder polyps GALLSTONES Metabolomics UPLC-MS/MS
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