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• W1553291264 abstract "The placenta is a glucocorticoid target organ, and glucocorticoids (GCs) are essential for the development and maturation of fetal organs. They are widely used for treatment of a variety of diseases during pregnancy. In various tissues, GCs have regulated by glucose transport systems; however, their effects on glucose transporters in the human placental endothelial cells (HPECs) are unknown. In the present study, HPECs were cultured 24 h in the presence or absence of 0·5, 5 and 50 µmol·l–1 of synthetic GC triamcinolone (TA). The glucose carrier proteins GLUT 1, GLUT 3 and GC receptor (GR) were detected in the HPECs. We showed increased expression of GLUT 1 and GLUT 3 proteins and messenger RNA (mRNA) levels (p < 0·05) after 24-h cell culture in the presence of 0·5, 5 and 50 µmol·l-1 of TA. In contrast, GR protein and mRNA expressions were down-regulated (p < 0·05) with 0·5, 5 and 50 µmol·l–1 of TA 24-h cell culture. The results demonstrate that GCs are potent regulators of placental GLUT 1 and GLUT 3 expression through GR. Excessive exposure to GCs causes maternal and fetal hypoglycemia and diminished fetal growth. We speculate that to compensate for fetal hypoglycemia and diminished fetal growth, the expression of placental endothelial glucose transporters might be increased. Copyright © 2011 John Wiley & Sons, Ltd." @default.
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• W1553291264 date "2011-10-10" @default.
• W1553291264 modified "2023-10-18" @default.
• W1553291264 title "Triamcinolone up-regulates GLUT 1 and GLUT 3 expression in cultured human placental endothelial cells" @default.
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• W1553291264 doi "https://doi.org/10.1002/cbf.1817" @default.
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