Nuclear magnetic resonance-based metabolomics for prediction of gastric damage induced by indomethacin in rats

So Young Um, Jung Hyun Park, Myeon Woo Chung, Kyu Bong Kim, Seon Hwa Kim, Ki Hwan Choi, Hwa Jeong Lee

Research output: Contribution to journalArticlepeer-review

20 Scopus citations


Non-steroidal anti-inflammatory drugs (NSAIDs) have side effects including gastric erosions, ulceration and bleeding. In this study, pattern recognition analysis of the 1H-nuclear magnetic resonance (NMR) spectra of urine was performed to develop surrogate biomarkers related to the gastrointestinal (GI) damage induced by indomethacin in rats. Urine was collected for 5h after oral administration of indomethacin (25mgkg -1) or co-administration with cimetidine (100mgkg -1), which protects against GI damage. The 1H-NMR urine spectra were divided into spectral bins (0.04ppm) for global profiling, and 36 endogenous metabolites were assigned for targeted profiling. The level of gastric damage in each animal was also determined. Indomethacin caused severe gastric damage; however, indomethacin administered with cimetidine did not. Simultaneously, the patterns of changes in their endogenous metabolites were different. Multivariate data analyses were carried out to recognize the spectral pattern of endogenous metabolites related to indomethacin using partial least square-discrimination analysis. In targeted profiling, a few endogenous metabolites, 2-oxoglutarate, acetate, taurine and hippurate, were selected as putative biomarkers for the gastric damage induced by indomethacin. These metabolites changed depending on the degree of GI damage, although the same dose of indomethacin (10mgkg -1) was administered to rats. The results of global and targeted profiling suggest that the gastric damage induced by NSAIDs can be screened in the preclinical stage of drug development using a NMR based metabolomics approach.

Original languageEnglish
Pages (from-to)87-94
Number of pages8
JournalAnalytica Chimica Acta
StatePublished - 13 Apr 2012

Bibliographical note

Funding Information:
This study was supported by a 2008 grant ( 08171KFDA522 ) from the Korea Food & Drug Administration and in part by the Brain Korea 21 program from the Korean Ministry of Education, Science and Technology.


  • Biomarker
  • Cimetidine· Gastric damage
  • Indomethacin
  • Metabolomics
  • NMR


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