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Metformin modulates insulin post-receptor signaling transduction in chronically insulin-treated Hep G2 cells.

  
@article{APS9023,
	author = {Li Yuan and Reinhard Ziegler and Andreas Hamann},
	title = {Metformin modulates insulin post-receptor signaling transduction in chronically insulin-treated Hep G2 cells.},
	journal = {Acta Pharmacologica Sinica},
	volume = {24},
	number = {1},
	year = {2016},
	keywords = {},
	abstract = {AIM: To study the effect of chronic insulin treatment on insulin post-receptor signaling transduction and whether the effects of metformin are transmitted throughout the cascade of insulin signaling intermediates in a human hepatoma cell line (Hep G2). METHODS: Hep G2 cells were incubated in serum free media containing either insulin 100 nmol/L or insulin 100 nmol/L plus different concentrations (0.01-10 mmol/L) of metformin for 16 h and then were stimulated with insulin 100 nmol/L for 1 min. RESULTS: Chronic treatment of insulin 100 nmol/L induced a significant reduction in the phosphorylation and protein expression of IR?, IRS1 and IRS2, which therefore resulted in a downregulation of association of PI3K with IRS. Therapeutic concentrations (0.01-0.1 mmol/L) of metformin prevented the changes induced by chronic insulin treatment in these post-receptor components of insulin signaling pathway. Tyrosine phosphorylation of IR?, IRS1, and IRS2 was increased by 2.7 fold (P < 0.01), 6.8 fold (P < 0.01), and 2.3 fold (P },
	issn = {1745-7254},	url = {http://www.chinaphar.com/article/view/9023}
}