Anti-diabetic effect of loganin by inhibiting FOXO1 nuclear translocation via PI3K/Akt signaling pathway in INS-1 cell

نویسندگان

  • Dan-Dan Zhao Beijing University of Chinese Medicine, Beijing, 100029, China
  • Fang-Fang Mo Beijing University of Chinese Medicine, Beijing, 100029, China
  • Hai-Xia Liu Beijing University of Chinese Medicine, Beijing, 100029, China
  • Jing Hua Beijing University of Chinese Medicine, Third Affiliated Hospital, Beijing, 100029, China
  • Sihua Gao Beijing University of Chinese Medicine, Beijing, 100029, China
  • Tian An Beijing University of Chinese Medicine, Beijing, 100029, China
  • Tian Tian Beijing University of Chinese Medicine, Beijing, 100029, China
  • Yi Zhang Beijing Open University, Beijing, 100081, China
چکیده مقاله:

Objective(s): JiangTangXiaoKe (JTXK) granule, a Chinese traditional herbal formula, has been clinically used and demonstrated to be beneficial in controlling high glucose and to relieve the symptoms of  Type 2 diabetes mellitus patients for decades. In this study, we explored how loganin, one of the components in JTXK granule, mediated the anti-diabetic effect.Materials and Methods: We generate a cell model with the dysfunction of insulin secretion by over-expression FOXO1 in INS-1 cells. MTT method was used to detect cytotoxicity after treated with Loganin. ELISA analysis was used to examine insulin secretion. The expression levels of FOXO1 and Akt were evaluated by Western blot.Results: Treatment with Loganin did not change the expression level of FOXO1 in INS-1 cells, but increased phosphorylation of FOXO1 and inhibited the nuclear translocation and accumulation of FOXO1, which improved the insulin secretion of the cells. Mechanistically, we found PI3K/Akt signaling pathway involved in these effects, which were blocked by an Akt inhibitor, LY294002.Conclusion: Loganin mediated the subcellular distribution of FOXO1 via PI3K/Akt signaling pathway, which protected the function of insulin secretion in islet INS-1 cells.

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عنوان ژورنال

دوره 22  شماره 3

صفحات  262- 266

تاریخ انتشار 2019-03-01

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