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Metabolomic profiling distinction of human nonalcoholic fatty liver disease progression from a common rat model.

JianHua HanAnika L DzierlengaZhengqiang LuDean D BillheimerElmira TorabzadehApril D LakeHui LiPetr NovakPetia ShipkovaNelly AranibarDonald RobertsonMichael D ReilyLois D Lehman-McKeemanNathan J Cherrington
Published in: Obesity (Silver Spring, Md.) (2017)
Overall, these results indicate that metabolites of specific pathways may be useful biomarkers for NASH progression, although these markers may not correspond to rodent NASH models. The MCD model may be useful when studying certain end points of NASH; however, the metabolomics results indicate important differences between humans and rodents in the biochemical pathogenesis of the disease.
Keyphrases
  • endothelial cells
  • ms ms
  • mass spectrometry
  • induced pluripotent stem cells
  • liver fibrosis