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

被引:3
作者
Asano, Tomomi [1 ,2 ]
Taki, Kentaro [2 ]
Kitamori, Kazuya [1 ]
Naito, Hisao [1 ]
Nakajima, Tamie [3 ]
Tsuchihashi, Hitoshi [2 ]
Ishii, Akira [2 ]
Zaitsu, Kei [2 ,4 ]
机构
[1] Kinjo Gakuin Univ, Dept Human Life & Environm, Nagoya, Aichi 4638521, Japan
[2] Nagoya Univ, Dept Legal Med & Bioeth, Grad Sch Med, Nagoya, Aichi 4668550, Japan
[3] Chubu Univ, Coll Life & Hlth Sci, Kasugai, Aichi 4878501, Japan
[4] Nagoya Univ, Inst Adv Res, In Vivo Real Time Omics Lab, Nagoya, Aichi 4648601, Japan
来源
ACS OMEGA | 2021年 / 6卷 / 12期
关键词
FIBROTIC STEATOHEPATITIS; METABOLOME ANALYSIS; MOUSE-LIVER; PLASMA; URINE; SERUM; MS; IONIZATION; BIOMARKER; DIET;
D O I
10.1021/acsomega.1c00403
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We developed a highly sensitive method for quantifying 21 bile acids (BAs) in the rat liver by capillary liquid chromatography tandem mass spectrometry (cLC/MS/MS) with one-pot extraction. High recovery rates were obtained for the one-pot methods with either methanol (MeOH) extraction or MeOH/acetonitrile (ACN) (1:1, v/v) mixture extraction; the results obtained for the MeOH/ACN mixture solution were better than the results obtained for MeOH. Thus, we determined that the one-pot method with MeOH/ACN was the most suitable method for the efficient extraction of BAs in the liver. Targeted BAs were well separated by cLC with gradient elution using ammonium acetate (NH4OAc)-MeOH mobile phases. Method validation proved that the intra-day and inter-day accuracies and precisions were primarily less than +/- 20 and 20% relative standard deviation, respectively. Also, the limit of detection (LOD) and the limit of quantitation (LOQ) were 0.9-10 and 2.3-27 ng/g liver, which proves the high sensitivity of the method. Finally, we quantitated 21 BA concentrations in the liver samples of normal and nonalcoholic steatohepatitis (NASH) rats, both of which were derived from stroke-prone spontaneously hypertensive five (SHRSP5) /Dmcr rat. The hepatic BA profiles were found to be substantially different between the normal and NASH groups; the two groups were clearly separated along the first component axis in the score plots of the principal component analysis. In particular, 10 BAs (beta-muricholic acid (MCA), glyco (G-) cholic acid (CA), G-chenodeoxycholic acid (CDCA), tauro (T-) CA, T-CDCA, T-ursodeoxycholic acid (UDCA), T-lithocholic acid (LCA), T-hiodeoxycholic acid (HDCA), T-alpha-MCA, and T-beta-MCA) were significantly different between the two groups using Welch's t-test with the false discovery rate correction method, demonstrating BA disruption in the NASH model rat. In conclusion, this method was able to quantify 21 BAs in the rat liver and will evaluate the hepatic BA pathophysiology of rat disease models.
引用
收藏
页码:8588 / 8597
页数:10
相关论文
共 43 条
  • [1] Quantitative-profiling of bile acids and their conjugates in mouse liver, bile, plasma, and urine using LC-MS/MS
    Alnouti, Yazen
    Csanaky, Ivan L.
    Klaassen, Curtis D.
    [J]. JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2008, 873 (02): : 209 - 217
  • [2] Bile acid preparation and comprehensive analysis by high performance liquid chromatography-high-resolution mass spectrometry
    Amplatz, Benno
    Zohrer, Evelyn
    Haas, Christina
    Schaffer, Maria
    Stojakovic, Tatjana
    Jahnel, Jorg
    Fauler, Guenter
    [J]. CLINICA CHIMICA ACTA, 2017, 464 : 85 - 92
  • [3] High sensitive analysis of rat serum bile acids by liquid chromatography/electrospray ionization tandem mass spectrometry
    Ando, M
    Kaneko, T
    Watanabe, R
    Kikuchi, S
    Goto, T
    Iida, T
    Hishinuma, T
    Mano, N
    Goto, J
    [J]. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2006, 40 (05) : 1179 - 1186
  • [4] CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING
    BENJAMINI, Y
    HOCHBERG, Y
    [J]. JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) : 289 - 300
  • [5] Analysis of the solubilization of steroids by bile salt micelles
    Cai, XH
    Grant, DJW
    Wiedmann, TS
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 1997, 86 (03) : 372 - 377
  • [6] Instrumental requirements for nanoscale liquid chromatography
    Chervet, JP
    Ursem, M
    Salzmann, JB
    [J]. ANALYTICAL CHEMISTRY, 1996, 68 (09) : 1507 - 1512
  • [8] Capillary LC coupled with high-mass measurement accuracy mass spectrometry for metabolic profiling
    Ding, Jie
    Sorensen, Christina M.
    Zhang, Qibin
    Jiang, Hongliang
    Jaitly, Navdeep
    Livesay, Eric A.
    Shen, Yufeng
    Smith, Richard D.
    Metz, Thomas O.
    [J]. ANALYTICAL CHEMISTRY, 2007, 79 (16) : 6081 - 6093
  • [9] Targeted profiling of circulating and hepatic bile acids in human, mouse, and rat using a UPLC-MRM-MS-validated method
    Garcia-Canaveras, Juan C.
    Teresa Donato, M.
    Castell, Jose V.
    Lahoz, Agustin
    [J]. JOURNAL OF LIPID RESEARCH, 2012, 53 (10) : 2231 - 2241
  • [10] Bile acids: analysis in biological fluids and tissues
    Griffiths, William J.
    Sjovall, Jan
    [J]. JOURNAL OF LIPID RESEARCH, 2010, 51 (01) : 23 - 41