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Am J Physiol Endocrinol Metab 281: E217-E223, 2001;
0193-1849/01 $5.00
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Vol. 281, Issue 2, E217-E223, August 2001

Fetal hyperinsulinemia increases farnesylation of p21 Ras in fetal tissues

Elizabeth Stephens, Patti J. Thureen, Marc L. Goalstone, Marianne S. Anderson, J. Wayne Leitner, William W. Hay Jr., and Boris Draznin

Veterans Affairs Research Service, Department of Medicine, Perinatal Research Center, Department of Pediatrics, University of Colorado Health Sciences Center, Denver, Colorado 80220

Even though the role of fetal hyperinsulinemia in the pathogenesis of fetal macrosomia in patients with overt diabetes and gestational diabetes mellitus seems plausible, the molecular mechanisms of action of hyperinsulinemia remain largely enigmatic. Recent indications that hyperinsulinemia "primes" various tissues to the mitogenic influence of growth factors by increasing the pool of prenylated Ras proteins prompted us to investigate the effect of fetal hyperinsulinemia on the activitiy of farnesyltransferase (FTase) and the amounts of farnesylated p21 Ras in fetal tissues in the ovine experimental model. Induction of fetal hyperinsulinemia by direct infusion of insulin into the fetus and by either fetal or maternal infusions of glucose resulted in significant increases in the activity of FTase and the amounts of farnesylated p21 Ras in fetal liver, skeletal muscle, fat, and white blood cells. An additional infusion of somatostatin into hyperglycemic fetuses blocked fetal hyperinsulinemia and completely prevented these increases, specifying insulin as the causative factor. We conclude that the ability of fetal hyperinsulinemia to increase the size of the pool of farnesylated p21 Ras may prime fetal tissues to the action of other growth factors and thereby constitute one mechanism by which fetal hyperinsulinemia could induce macrosomia in diabetic pregnancies.

insulin; prenylation; fetal macrosomia


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