Investigation of metabolite alteration in dimethylnitrosamine-induced liver fibrosis by GC-MS

Hyun Kyoung Ju, Ha Wook Chung, Hee Seung Lee, Johan Lim, Jeong Hill Park, Sung Cil Lim, Joon Mee Kim, Soon Sun Hong, Sung Won Kwon

Research output: Contribution to journalArticle

5 Scopus citations

Abstract

Background: A metabolomic study of biomarkers associated with dimethylnitrosamine (DMN)-induced hepatic fibrosis in Sprague-Dawley rats was performed using GC-MS. The clinical chemistry of the collected blood and the histopathology of excised liver samples were examined, and urine samples were prepared by solvent extraction. Results: Through pattern analysis, the DMN-treated group was divided into two subgroups based on the aspartate aminotransferase (AST) levels compared with the control, a moderately higher group (DMN subgroup A) and a significantly higher group (DMN subgroup B). Uric acid, orotic acid, N-phenylacetylglycine and glutaric acid were biomarkers for DMN subgroup A, aminomalonic acid was a biomarker for DMN subgroup B, and arabitol level distinguished control versus DMN treatment regardless of AST level. Conclusion: This study suggests that the identification and profiling of AST level-related metabolites may be useful as a diagnostic tool and for the study of the mechanism of liver fibrosis induced by DMN.

Original languageEnglish (US)
Pages (from-to)41-51
Number of pages11
JournalBioanalysis
Volume5
Issue number1
DOIs
StatePublished - Jan 1 2013

ASJC Scopus subject areas

  • Analytical Chemistry
  • Pharmacology, Toxicology and Pharmaceutics(all)
  • Clinical Biochemistry
  • Medical Laboratory Technology

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    Ju, H. K., Chung, H. W., Lee, H. S., Lim, J., Park, J. H., Lim, S. C., Kim, J. M., Hong, S. S., & Kwon, S. W. (2013). Investigation of metabolite alteration in dimethylnitrosamine-induced liver fibrosis by GC-MS. Bioanalysis, 5(1), 41-51. https://doi.org/10.4155/bio.12.296