Horm Metab Res 1993; 25(3): 165-169
DOI: 10.1055/s-2007-1002069
Clinical

© Georg Thieme Verlag, Stuttgart · New York

In Vivo and In Vitro Effects of Glucocorticoids on Glucose Transport in Human Polymorphonuclear Leukocytes

Y. Okuno, Y. Nishizawa, T. Kawagishi, H. Morii
  • The Second Department of Internal Medicine, Osaka City University Medical School, Osaka, Japan
Weitere Informationen

Publikationsverlauf

1992

1992

Publikationsdatum:
14. März 2008 (online)

Summary

In order to study whether or not exogenous and/or endogenous glucocorticoids affect the glucose transport rate in human cells, we examined the transport rate of a non-metabolizable hexose analogue, 3-O-methyl-D-glucose, in polymorphonuclear leukocytes from patients with hypercortisolism. The mean glucose transport rate was prominently decreased in 5 patients with Cushing's syndrome compared with 29 healthy controls (5.4±1.8 vs 10.4±2.5 fl/cell · sec, mean±SD, p<0.001) and the transport rate returned to normal range after adenoma resection in 2 of them. In 10 patients with nephrotic syndrome treated with prednisolone, a significant negative correlation was found between transport rates and daily prednisolone doses. When prednisolone of 40 mg/day was administered to a diabetic patient and the dose was gradually reduced, glucose transport rate was transiently decreased during the initial period. In an in vitro study, a synthetic glucocorticoid, dexamethasone, directly inhibited glucose transport rate in those cells in time- and concentration-dependent manners by mainly reducing max. These results suggest that either exogenous or endogenous hypercortisolism in humans is associated with a decrease in glucose transport rate in polymorphonuclear leukocytes, and that the direct effect of glucocorticoids accounts at least in part for the decreased glucose transport rates found in those cells.

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