Attenuation of hepatic expression and secretion of selenoprotein P by metformin

被引:38
作者
Speckmann, Bodo [1 ]
Sies, Helmut [1 ,2 ,3 ]
Steinbrenner, Holger [1 ]
机构
[1] Univ Dusseldorf, Inst Biochem & Mol Biol 1, D-40225 Dusseldorf, Germany
[2] Univ Dusseldorf, IUF, D-40225 Dusseldorf, Germany
[3] King Saud Univ, Riyadh, Saudi Arabia
关键词
Selenium; Glucose; Selenophosphate synthetase; Type; 2; diabetes; Metformin; Insulin; Glutathione peroxidase; INDUCED INSULIN-RESISTANCE; TYROSINE-PHOSPHATASE; 1B; IN-VIVO; GLUTATHIONE-PEROXIDASE; SELENIUM; PLASMA; MECHANISM; PROTEIN; CELLS; MEMBRANE;
D O I
10.1016/j.bbrc.2009.06.143
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
High serum selenium levels have been associated epidemiologically with increased incidence of type 2 diabetes. The Major fraction of total selenium in serum is represented by liver-derived selenoprotein P (SeP). This study Was undertaken to test for a hypothesized effect of hyperglycemia and the antihyperglycemic drug metformin on hepatic selenoprotein P biosynthesis. Cultivation of rat hepatocytes in the presence of high glucose concentrations (25 mmol/l) resulted in increased selenoprotein P mRNA expression and secretion. Treatment with metformin close-dependently down-regulated SeP? mRNA expression and secretion, and Suppressed glucocorticoid-stimulated production of SeP. Moreover, metformin strongly decreased mRNA levels of selenophosphate synthetase 2 (SPS-2), an enzyme essential for selenoprotein biosynthesis. Taken together, these results indicate an influence of metformin on selenium metabolism in hepatocytes. As selenoprotein P is the major transport form of selenium, metformin treatment may thereby diminish selenium supply to extrahepatic tissues. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:158 / 163
页数:6
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