Intracerebroventricular infusion of a triglyceride emulsion leads to both altered insulin secretion and hepatic glucose production in rats

Pflugers Arch. 2002 Dec;445(3):375-80. doi: 10.1007/s00424-002-0937-3. Epub 2002 Nov 1.

Abstract

We investigated here whether non-esterified fatty acids (NEFA) influence insulin secretion and action through a direct effect on central nervous system sites involved in the control of glucose homeostasis. Normal Wistar rats received a 48-h intracerebroventricular infusion of either a 10% triglyceride (Intralipid, IL)/heparin emulsion (IL/h) or saline/heparin solution (control). At 48 h, insulin secretion as measured by an intravenous glucose tolerance test, was more elevated in IL/h than in control rats. Pancreatic noradrenaline turnover was decreased by 57% in IL/h rats, suggesting low pancreatic sympathetic output that could account partly for the elevated insulin secretion. The time course of glycaemia was similar in both groups, suggesting insulin resistance. Euglycaemic-hyperinsulinaemic clamps were imposed to assess peripheral and hepatic insulin sensitivity. At each insulin concentration glucose utilization was increased to a similar extent in both groups, whereas hepatic glucose production decreased much less in IL/h than in control rats. Hepatic insulin insensitivity could be related partly to activation of the hypothalamic-pituitary-adrenocortical axis, since plasma corticosterone concentration was significantly increased in IL/h rats compared with controls. Our data indicate that lipids may alter both insulin secretion and hepatic sensitivity to insulin through their effect on central nervous system.

MeSH terms

  • Animals
  • Blood / metabolism
  • Blood-Brain Barrier
  • Fat Emulsions, Intravenous / administration & dosage*
  • Glucose / biosynthesis*
  • Glucose Clamp Technique
  • Injections, Intraventricular
  • Insulin / metabolism*
  • Insulin Secretion
  • Liver / drug effects
  • Liver / metabolism*
  • Male
  • Norepinephrine / metabolism
  • Palmitates / pharmacokinetics
  • Pancreas / metabolism
  • Rats
  • Rats, Wistar

Substances

  • Fat Emulsions, Intravenous
  • Insulin
  • Palmitates
  • Glucose
  • Norepinephrine