Liver-specific metabolomics characterizes the hepatotoxicity of Dioscorea bulbifera rhizome in rats by integration of GC-MS and 1H-NMR

• Published in: Journal of ethnopharmacology Vol. 226; pp. 111 - 119
• Main Authors: Zhao, Dong-Sheng, Wu, Zi-Tian, Li, Zhuo-Qing, Wang, Ling-Li, Jiang, Li-Long, Shi, Wei, Li, Ping, Li, Hui-Jun
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 15.11.2018
• Subjects: 1H-NMR; Dioscorea bulbifera rhizome; GC-MS; Hepatotoxicity; Integrated analysis; Live-specific metabolomics; AST; Live-specific metabolomics; ALP; OPLS-DA; ALT; Dioscorea bulbifera rhizome; Integrated analysis; PCA; GC-MS; TBA; QC; 1H-NMR; DBR; GGT; TBIL; VIP; Hepatotoxicity; TCM
• ISSN: 0378-8741; 1872-7573
• DOI: 10.1016/j.jep.2018.08.014

Dioscorea bulbifera rhizome (DBR), one type of herbal medicine, is extensively used in both Indian and Chinese system of traditional medicine. It has been effective in treating various diseases, such as sore throat, struma, and tumors. However, more and more clinical investigations have suggested that DBR can cause liver injury. In the present study, we aimed to characterize the corresponding molecular changes of liver dysfunction and reveal overall metabolic and physiological mechanisms of the subchronic toxic effect of DBR. A liver-specific metabolomics approach integrating GC-MS and 1H-NMR was developed to assess the hepatotoxicity in rats after DBR exposure for 12 weeks. Multivariate statistical analysis and pattern recognition were employed to examine different metabolic profiles of liver in DBR-challenged rats. A total of 61 metabolites were screened as significantly altered metabolites, which were distributed in 43 metabolic pathways. The correlation network analysis indicated that the hub metabolites of hepatotoxicity could be mainly linked to amino acid, lipid, purine, pyrimidine, bile acid, gut microflora, and energy metabolisms. Notably, purine, pyrimidine, and gut microflora metabolisms might be novel pathways participating in metabolic abnormalities in rats with DBR-triggered hepatic damage. Our results primarily showed that the liver-specific metabolic information provided by the different analytical platforms was essential for identifying more biomarkers and metabolic pathways, and our findings provided novel insights into understand the mechanistic complexity of herb-induced liver injury. [Display omitted] •Liver tissue-specific metabolomics characterized the hepatotoxicity of DBR in rats.•GC-MS integrated 1H-NMR to investigate the metabolic profile of rat liver.•Metabolic network was disturbed in liver due to the aberrant regulation of multiple systems.•Integrated two analytical platforms for metabolomics provided greater insights.