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Endocrinology, doi:10.1210/endo-128-2-689
Endocrinology Vol. 128, No. 2 689-696
Copyright © 1991 by the Endocrine Society.
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Enhanced Expression of Insulin-Like Growth Factor-Binding Protein-I in the Fasted Rat: The Effects of Insulin and Growth Hormone Administration*

LIAM J. MURPHY{dagger}, CHARITA SENEVIRATNE, PAUL MOREIRA and RONALD E. REID

Departments of Internal Medicine and Physiology, Faculty of Medicine, and Faculty of Pharmacy (R.E.R.), University of Manitoba Winnipeg, Manitoba, Canada R3E OW3

Abstract

The effect of fasting on insulin-like growth factor- binding protein-1 (IGFBP-1) expression was examined in the rat. Food deprivation for a period of 24 h resulted in a 9.5 ± 2.0-fold increase in hepatic IGFBP-1 mRNA abundance (P < 0.001). An increase in circulating IGFBP-1 in sera from fasted rats was demonstrated by immunoblotting, and an increased abundance of a 30-kDa IGFBP in sera from fasted rats was apparent when [125I]IGF-I was used in ligand blotting experiments. Refeeding resulted in a prompt decline in hepatic IGFBP- 1 mRNA. Administration of insulin (0.5-4 U, ip) to fasted rats resulted in profound hypoglycemia, but either increased or had no significant effect on hepatic IGFBP-1 mRNA abundance. In contrast, administration of human GH (hGH; 100 µg, ip) resulted in a prompt decline in hepatic IGFBP-1 mRNA, followed by a late rebound in IGFBP-1 mRNA to levels greater than those in fasted controls. Furthermore, hepatic IGFBP-1 mRNA levels were significantly lower in hGH-treated (100 µg every 8 h) fooddeprived rats than in saline-treated food-deprived rats (2.25 ± 1.55- vs. 8.99 ± 3.80-fold increase; P < 0.005). Similar changes were observed when serum IGFBP-1 was quantitated by immunoblotting. The effects of GH could not be explained by secondary hyperinsulinism, since no significant increase in insulin levels was observed in GH-treated rats. From these observations we conclude the enhanced expression of IGFBP-1 in the fooddeprived rat may be a consequence of GH deficiency rather than insulin deficiency. (Endocrinology 128: 689–696, 1991)

Footnotes

* This work was supported by grants from the Medical Research Council and the Canadian Diabetes Association.

{dagger} Recipient of a Medical Research Council scholarship award.

Received July 26, 1990.




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