Rosiglitazone stimulates the release and synthesis of insulin by enhancing GLUT-2, glucokinase and BETA2/NeuroD expression

Peroxisome proliferator-activated receptor (PPAR)-γ is a member of the nuclear receptor superfamily, and its ligands, the thiazolidinediones, might directly stimulate insulin release and insulin synthesis in pancreatic β-cells. In the present study, we examined the effects of rosiglitazone (RGZ) on...

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Veröffentlicht in:Biochemical and biophysical research communications 2008-03, Vol.367 (3), p.623-629
Hauptverfasser: Kim, Hyo-Sup, Noh, Jung-Hyun, Hong, Seung-Hyun, Hwang, You-Cheol, Yang, Tae-Young, Lee, Myung-Shik, Kim, Kwang-Won, Lee, Moon-Kyu
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Sprache:eng
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Zusammenfassung:Peroxisome proliferator-activated receptor (PPAR)-γ is a member of the nuclear receptor superfamily, and its ligands, the thiazolidinediones, might directly stimulate insulin release and insulin synthesis in pancreatic β-cells. In the present study, we examined the effects of rosiglitazone (RGZ) on insulin release and synthesis in pancreatic β-cell (INS-1). Insulin release and synthesis were stimulated by treatment with RGZ for 24h. RGZ upregulated the expressions of GLUT-2 and glucokinase (GCK). Moreover, it was found that RGZ increased the expression of BETA2/NeuroD gene which could regulate insulin gene expression. These results suggest that RGZ could stimulate the release and synthesis of insulin through the upregulation of GLUT-2, GCK, and BETA2/NeuroD gene expression.
ISSN:0006-291X
1090-2104
DOI:10.1016/j.bbrc.2007.12.192