| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2569493 | Toxicology and Applied Pharmacology | 2011 | 9 Pages |
An investigative renal toxicity study using metabolomics was conducted with a potent nicotinic acid receptor (NAR) agonist, SCH 900424. Liquid chromatography-mass spectrometry (LC–MS) and gas chromatography-mass spectrometry (GC–MS) techniques were used to identify small molecule biomarkers of acute kidney injury (AKI) that could aid in a better mechanistic understanding of SCH 900424-induced AKI in mice. The metabolomics study revealed 3-indoxyl sulfate (3IS) as a more sensitive marker of SCH 900424-induced renal toxicity than creatinine or urea. An LC–MS assay for quantitative determination of 3IS in mouse matrices was also developed. Following treatment with SCH 900424, 3IS levels were markedly increased in murine plasma and brain, thereby potentially contributing to renal- and central nervous system (CNS)-related rapid onset of toxicities. Furthermore, significant decrease in urinary excretion of 3IS in those animals due to compromised renal function may be associated with the elevation of 3IS in plasma and brain. These data suggest that 3IS has a potential to be a marker of renal and CNS toxicities during chemically-induced AKI in mice. In addition, based on the metabolomic analysis other statistically significant plasma markers including p-cresol-sulfate and tryptophan catabolites (kynurenate, kynurenine, 3-indole-lactate) might be of toxicological importance but have not been studied in detail. This comprehensive approach that includes untargeted metabolomic and targeted bioanalytical sample analyses could be used to investigate toxicity of other compounds that pose preclinical or clinical development challenges in a pharmaceutical discovery and development.
Research highlights► Nicotinic acid receptor agonist, SCH 900424, caused acute kidney injury in mice. ► MS-based metabolomics was conducted to identify potential small molecule markers of renal toxicity. ► 3-indoxyl-sulfate was found to be as a more sensitive marker of renal toxicity than creatinine or urea. ► 3-IS levels were increased not only in murine plasma but also in the brain. ► 3-IS potentially contributes to renal-and CNS-related rapid onset of toxicities.
