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Evaluation of metabolomic profiling against renal toxicity in Sprague-Dawley rats treated with melamine and cyanuric acid

Authors
Kim, TH[Kim, Tae Hyung]Ahn, MY[Ahn, Mee Young]Lim, HJ[Lim, Hyun Jung]Lee, YJ[Lee, Young Ju]Shin, YJ[Shin, Yu Jin]De, U[De, Umasankar]Lee, J[Lee, Jaewon]Lee, BM[Lee, Byung Mu]Kim, S[Kim, Suhkmann]Kim, HS[Kim, Hyung Sik]
Issue Date
Dec-2012
Publisher
SPRINGER HEIDELBERG
Keywords
Melamine; Nephrotoxicity; Metabolomics; [H-1]NMR
Citation
ARCHIVES OF TOXICOLOGY, v.86, no.12, pp.1885 - 1897
Indexed
SCIE
SCOPUS
Journal Title
ARCHIVES OF TOXICOLOGY
Volume
86
Number
12
Start Page
1885
End Page
1897
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/63407
DOI
10.1007/s00204-012-0910-7
ISSN
0340-5761
Abstract
Melamine-induced renal toxicity is associated with crystal formation in the kidney following exposure to melamine and cyanuric acid. However, metabolomic profiling of intact kidney tissue after chronic intake of melamine and cyanuric acid (M + CA) mixtures has rarely been studied. The present study investigated the melamine-induced renal toxicity by determining metabolites in the kidney through [H-1]nuclear magnetic resonance. Melamine (63 mg/kg) and cyanuric acid (6.3 mg/kg) were co-administered to rats via oral gavage for 30 days. The mixture of M + CA (63/6.3 mg/kg) induced nephrotoxicity, as determined by increased blood urea nitrogen (BUN) and creatinine levels. The kidney weights were significantly increased in the animals treated with M + CA (63/6.3 mg/kg). The histological analysis revealed epithelial degeneration and necrotic cell death in the proximal and distal tubules. Furthermore, various metabolites were altered in both renal medullar and cortical tissues. In the medullar tissues, asparagine, choline, creatinine, cysteine, ethanolamine, glucose, isoleucine, glutamine, and myo-inositol levels were elevated, but glucitol, phenylalanine, tyrosine, and sn-glycero-3-levels were reduced. In the cortex, ethanolamine, hypoxanthine, isoleucine and o-phosphoethanolamine levels were increased, whereas formate, glucose, glutathione, threonine, and myo-inositol levels were decreased, suggesting the M + CA-induced renal cell injury. These data suggest that a mixture of M + CA-induced metabolites may be useful biomarkers for the detection of kidney injury.
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