Skip to main navigation Skip to search Skip to main content

An extract from wax apple (Syzygium samarangense (Blume) Merrill and Perry) effects glycogenesis and glycolysis pathways in tumor necrosis factor-α-treated FL83B mouse hepatocytes

  • Szu Chuan Shen*
  • , Wen Chang Chang
  • , Chiao Li Chang
  • *Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    Abstract

    FL83B mouse hepatocytes were treated with tumor necrosis factor-α (TNF-α) to induce insulin resistance to investigate the effect of a wax apple aqueous extract (WAE) in insulin-resistant mouse hepatocytes. The uptake of 2-[N-(7-nitrobenz-2-oxa-1, 3-diazol-4-yl)amino]-2-deoxyglucose (2 NBDG), a fluorescent D-glucose derivative, was performed, and the metabolism of carbohydrates was evaluated by examining the expression of glycogenesis or glycolysis-related proteins in insulin-resistant hepatocytes. The results show that WAE significantly improves the uptake of glucose and enhances glycogen content in insulin-resistant FL83B mouse hepatocytes. The results from Western blot analysis also reveal that WAE increases the expression of glycogen synthase (GS), hexokinase (HXK), glucose-6-phosphate dehydrogenase (G6PD), phosphofructokinase (PFK) and aldolase in TNF-α treated cells, indicating that WAE may ameliorate glucose metabolism by promoting glycogen synthesis and the glycolysis pathways in insulin-resistant FL83B mouse hepatocytes.

    Original languageEnglish
    Pages (from-to)455-467
    Number of pages13
    JournalNutrients
    Volume5
    Issue number2
    DOIs
    Publication statusPublished - 2013 Feb 6

    Keywords

    • FL83B mouse hepatocytes
    • Glucose metabolism
    • Glycogenesis
    • Glycolysis
    • Insulin resistance
    • Wax apple

    ASJC Scopus subject areas

    • Food Science
    • Nutrition and Dietetics

    Fingerprint

    Dive into the research topics of 'An extract from wax apple (Syzygium samarangense (Blume) Merrill and Perry) effects glycogenesis and glycolysis pathways in tumor necrosis factor-α-treated FL83B mouse hepatocytes'. Together they form a unique fingerprint.

    Cite this