Gas chromatography-mass spectrometry-based simultaneous quantitative analytical method for urinary oxysterols and bile acids in rats

Authors
Kumar, Bhowmik SalilChung, Bong ChulLee, Young-JooYi, Hong JaeLee, Byung-HoonJung, Byung Hwa
Issue Date
2011-01-15
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Citation
ANALYTICAL BIOCHEMISTRY, v.408, no.2, pp.242 - 252
Abstract
A simultaneous quantitative assay method for urinary oxysterols and bile acids using GC-MS was developed to investigate the mechanism of liver toxicity induced by drugs or chemicals. Sample preparations were optimized by exploring various extraction solvents, derivatization reagents, and hydrolysis methods to achieve reliable and maximum sensitivity for these two different compound classes. As a result, satisfactory accuracy, precision, and sensitivity were obtained in the validation. The method was then applied to quantify urinary oxysterols and bile acids produced from liver toxicity induced by atorvastatin (250 mg/kg/day). From the results, increases in bile acid levels and decreases in the concentration ratio between cholic acid and chenodeoxycholic acid, which are the distinguishing phenomena observed in serum or bile for liver toxicity, were also observed in urine. Additionally, the mechanism of liver toxicity was investigated with the urinary concentration ratio of product to precursor in the metabolic pathway from cholesterol to bile acids. The results indicated that enzyme activities related to the production and degradation of bile acids, not oxysterols, were significantly changed from liver toxicity. Thus, it was concluded that urinary levels of oxysterols and bile acids could be useful tools for checking liver toxicity and investigating its mechanism. (c) 2010 Elsevier Inc. All rights reserved.
Keywords
CHOLESTEROL OXIDATION-PRODUCTS; COA REDUCTASE INHIBITOR; DRUG-INDUCED HEPATOTOXICITY; LIVER-DISEASE; BEAGLE DOGS; NUCLEAR RECEPTORS; MEDICAL PROGRESS; PLASMA; ATORVASTATIN; METABOLISM; CHOLESTEROL OXIDATION-PRODUCTS; COA REDUCTASE INHIBITOR; DRUG-INDUCED HEPATOTOXICITY; LIVER-DISEASE; BEAGLE DOGS; NUCLEAR RECEPTORS; MEDICAL PROGRESS; PLASMA; ATORVASTATIN; METABOLISM; Oxysterols; Bile acids; Hepatotoxicity; GC-MS (gas chromatography-mass spectrometry); Urine
ISSN
0003-2697
URI
https://pubs.kist.re.kr/handle/201004/130726
DOI
10.1016/j.ab.2010.09.031
Appears in Collections:
KIST Article > 2011
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