Maternal diabetes-induced hyperglycemia and acute intracerebral hyperinsulinism suppress fetal brain neuropeptide Y concentrations

Endocrinology. 1997 Mar;138(3):963-9. doi: 10.1210/endo.138.3.5001.

Abstract

We examined the effect of streptozotocin-induced maternal diabetes of 6-day duration and 4- to 24-h intracerebroventricular and systemic hyperinsulinism on fetal brain neuropeptide Y (NPY) synthesis and concentrations. Maternal diabetes (n = 6) leading to fetal hyperglycemia (5-fold increase; P < 0.05) and normoinsulinemia caused a 40% decline (P < 0.05) in fetal brain NPY messenger RNA (mRNA) and a 50% decline (P < 0.05) in NPY radioimmunoassayable levels compared to levels in streptozotocin-treated nondiabetic (n = 7) and vehicle-treated control (n = 8) animals. In contrast, systemic hyperinsulinemia (n = 7) of 5- to 100-fold increase (P < 0.05) over the respective control (n = 7) with normoglycemia caused an insignificant (20-30%) decrease in fetal brain NPY mRNA and protein concentrations. However, fetal intracerebroventricular hyperinsulinism (n = 7) with no change in fetal glucose concentrations caused a 50-60% decline (P < 0.05) in only the NPY peptide levels, with no change in the corresponding mRNA amounts. We conclude that fetal hyperglycemia of 6-day duration and intracerebroventricular hyperinsulinism of 4-24 h suppress fetal brain NPY concentrations, the former by a pretranslational and the latter by either a translational/posttranslational mechanism or depletion of intracellular secretory stores. We speculate that fetal hyperglycemia and intracerebroventricular hyperinsulinism additively can inhibit various intrauterine and immediate postnatal NPY-mediated biological functions.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acute Disease
  • Animals
  • Brain / embryology*
  • Brain / metabolism
  • Brain Diseases / etiology
  • Brain Diseases / metabolism
  • Female
  • Fetal Diseases / etiology
  • Fetal Diseases / metabolism
  • Fetus / metabolism*
  • Hyperglycemia / etiology
  • Hyperinsulinism / etiology
  • Hyperinsulinism / metabolism
  • Neuropeptide Y / antagonists & inhibitors*
  • Neuropeptide Y / metabolism
  • Osmolar Concentration
  • Pregnancy
  • Pregnancy in Diabetics / complications
  • Pregnancy in Diabetics / metabolism*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Neuropeptide Y