Literature DB >> 27450898

Quantitative profiling of bile acids in rat bile using ultrahigh-performance liquid chromatography-orbitrap mass spectrometry: Alteration of the bile acid composition with aging.

Gakyung Lee1, Hyunbeom Lee2, Jongki Hong3, Soo Hyun Lee4, Byung Hwa Jung5.   

Abstract

Bile acids (BAs) play important roles in physiological functions, including the homeostasis of cholesterol and lipids and as ligands for G protein-coupled receptors (GPCRs). With the increasing importance of BAs, analytical methods for their quantification and screening have been developed. However, due to the diverse range and variety of BAs with different activation potency, a simple, effective, and sensitive method is required to screen BAs for accurate quantification and identification. This paper presents an application of ultrahigh-performance liquid chromatography-orbitrap mass spectrometry (UHPLC-LTQ-Orbitrap MS) for profiling BAs in bile. Using this method, along with the accurate quantification of 19 targeted BAs, 22 unknown BAs were detected and characterized by their fragmentation patterns. The method is beneficial for screening most of the BAs (quantitatively and qualitatively) in rat bile with simple preparation in a single run. The sample dilution ranges of each BA were optimized depending on the concentration of BAs in the bile to obtain good peak separation and accurate data. The method validation was performed successfully using charcoal-treated bile and the intra and inter-day coefficients of variation were less than 20% for all BAs while the recovery were above 88.5% except for the lithocholic acid. The method was applied to profile the age-dependent changes in the contents of rat BAs. Through statistical analysis, we found that as the rats aged, unconjugated BAs and glycine-conjugated BAs decreased or were unaffected, while taurine-conjugated BAs were increased in general. Among the unknown BAs, 5 of the taurine-conjugated BAs increased, while a glycine-conjugated BA decreased, in agreement with the trends of the targeted BAs.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Aging; Bile; Bile acids (BAs); UPLC–Orbitrap-MS

Mesh:

Substances:

Year:  2016        PMID: 27450898     DOI: 10.1016/j.jchromb.2016.07.017

Source DB:  PubMed          Journal:  J Chromatogr B Analyt Technol Biomed Life Sci        ISSN: 1570-0232            Impact factor:   3.205


  5 in total

1.  One-Pot Extraction and Quantification Method for Bile Acids in the Rat Liver by Capillary Liquid Chromatography Tandem Mass Spectrometry.

Authors:  Tomomi Asano; Kentaro Taki; Kazuya Kitamori; Hisao Naito; Tamie Nakajima; Hitoshi Tsuchihashi; Akira Ishii; Kei Zaitsu
Journal:  ACS Omega       Date:  2021-03-16

2.  Decline in Liver Mitochondria Metabolic Function Is Restored by Hochuekkito Through Sirtuin 1 in Aged Mice With Malnutrition.

Authors:  Miwa Nahata; Naoki Fujitsuka; Hitomi Sekine; Chika Shimobori; Katsuya Ohbuchi; Seiichi Iizuka; Sachiko Mogami; Shunsuke Ohnishi; Hiroshi Takeda
Journal:  Front Physiol       Date:  2022-03-01       Impact factor: 4.566

3.  Metabolomics study of the therapeutic mechanism of a Chinese herbal formula on collagen-induced arthritis mice.

Authors:  Zhen Jin; Ji-da Zhang; Xin Wu; Gang Cao
Journal:  RSC Adv       Date:  2019-01-28       Impact factor: 4.036

4.  Quantitative Profiling of Bile Acids in Feces of Humans and Rodents by Ultra-High-Performance Liquid Chromatography-Quadrupole Time-of-Flight Mass Spectrometry.

Authors:  Xiaoxu Zhang; Xiaoxue Liu; Jiufang Yang; Fazheng Ren; Yixuan Li
Journal:  Metabolites       Date:  2022-07-11

5.  Untargeted Profiling of Bile Acids and Lysophospholipids Identifies the Lipid Signature Associated with Glycemic Outcome in an Obese Non-Diabetic Clinical Cohort.

Authors:  Nicolas Christinat; Armand Valsesia; Mojgan Masoodi
Journal:  Biomolecules       Date:  2020-07-15
  5 in total

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