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A Gas Chromatography-Mass Spectrometry Based Study on Urine Metabolomics in Rats Chronically Poisoned with Hydrogen Sulfide

Gas chromatography-mass spectrometry (GS-MS) in combination with multivariate statistical analysis was applied to explore the metabolic variability in urine of chronically hydrogen sulfide- (H(2)S-) poisoned rats relative to control ones. The changes in endogenous metabolites were studied by partial...

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Detalles Bibliográficos
Autores principales: Deng, Mingjie, Zhang, Meiling, Sun, Fa, Ma, Jianshe, Hu, Lufeng, Yang, Xuezhi, Lin, Guanyang, Wang, Xianqin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4411453/
https://www.ncbi.nlm.nih.gov/pubmed/25954748
http://dx.doi.org/10.1155/2015/295241
Descripción
Sumario:Gas chromatography-mass spectrometry (GS-MS) in combination with multivariate statistical analysis was applied to explore the metabolic variability in urine of chronically hydrogen sulfide- (H(2)S-) poisoned rats relative to control ones. The changes in endogenous metabolites were studied by partial least squares-discriminate analysis (PLS-DA) and independent-samples t-test. The metabolic patterns of H(2)S-poisoned group are separated from the control, suggesting that the metabolic profiles of H(2)S-poisoned rats were markedly different from the controls. Moreover, compared to the control group, the level of alanine, d-ribose, tetradecanoic acid, L-aspartic acid, pentanedioic acid, cholesterol, acetate, and oleic acid in rat urine of the poisoning group decreased, while the level of glycine, d-mannose, arabinofuranose, and propanoic acid increased. These metabolites are related to amino acid metabolism as well as energy and lipid metabolism in vivo. Studying metabolomics using GC-MS allows for a comprehensive overview of the metabolism of the living body. This technique can be employed to decipher the mechanism of chronic H(2)S poisoning, thus promoting the use of metabolomics in clinical toxicology.