Effect of 5-100 mu M epigallocatechin gallate (EGCG) on hepatic glucose 6-phosphatase (G6Pase) system was investigated. EGCG inhibited G6Pase in intact but not in permeabilized rat liver microsomes, suggesting the interference with the transport. However, EGCG did not hinder microsomal glucose 6-phosphate (G6P) uptake. Instead, it increased the accumulation of radioactivity after the addition of [C-14]IG6P, presumably due to a slower release of [C-14]glucose, the product of luminal hydrolysis. Indeed, EGCG was found to inhibit microsomal glucose efflux. Since G6Pase activity is depressed by glucose in a concentration-dependent manner, we concluded that EGCG inhibits G6Pase through an elevated luminal glucose level.
Csala, M., Margittai, E., Senesi, S., Gamberucci, A., Banhegyi, G., Mandl, J., et al. (2007). Inhibition of hepatic glucose 6-phosphatase system by the green tea flavanol epigallocatechin gallate. FEBS LETTERS, 581(8), 1693-1698 [10.1016/j.febslet.2007.03.045].
Inhibition of hepatic glucose 6-phosphatase system by the green tea flavanol epigallocatechin gallate
Senesi, S.;Gamberucci, Alessandra;Benedetti, Angiolo
2007-01-01
Abstract
Effect of 5-100 mu M epigallocatechin gallate (EGCG) on hepatic glucose 6-phosphatase (G6Pase) system was investigated. EGCG inhibited G6Pase in intact but not in permeabilized rat liver microsomes, suggesting the interference with the transport. However, EGCG did not hinder microsomal glucose 6-phosphate (G6P) uptake. Instead, it increased the accumulation of radioactivity after the addition of [C-14]IG6P, presumably due to a slower release of [C-14]glucose, the product of luminal hydrolysis. Indeed, EGCG was found to inhibit microsomal glucose efflux. Since G6Pase activity is depressed by glucose in a concentration-dependent manner, we concluded that EGCG inhibits G6Pase through an elevated luminal glucose level.File | Dimensione | Formato | |
---|---|---|---|
FEBSL Csala 2007.pdf
non disponibili
Descrizione: articolo su rivista
Tipologia:
PDF editoriale
Licenza:
Creative commons
Dimensione
248.84 kB
Formato
Adobe PDF
|
248.84 kB | Adobe PDF | Visualizza/Apri Richiedi una copia |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
https://hdl.handle.net/11365/20419