Effects of muscarinic blockade on insulin secretion and on glucose-induced thermogenesis in lean and obese human subjects

Eur J Clin Invest. 1991 Dec;21(6):608-15. doi: 10.1111/j.1365-2362.1991.tb01417.x.

Abstract

To determine whether hyperinsulinaemia of human obesity is dependent on the activity of the parasympathetic nervous system, and whether activation of the parasympathetic nervous system plays a role in glucose-induced thermogenesis, the metabolic effect of a continuous intravenous glucose infusion [44.4 mumol kg-1 body weight (bw) min-1] with or without atropine infusion was assessed in 11 obese patients and 10 lean controls. Compared with lean controls, obese patients had increased basal and glucose-stimulated plasma insulin and C-peptide concentrations and increased plasma glucose concentrations during glucose infusion. Glucose oxidation during i.v. glucose was lower in obese patients than in lean controls. Glucose-induced thermogenesis was similar in obese patients and in lean controls. Atropine infusion did not affect basal plasma glucose, insulin or free fatty acid concentrations nor glucose-stimulated plasma glucose, insulin, C-peptide, glucagon or free fatty acid concentrations in both groups of subjects. Glucose and lipid oxidation rates and glucose-induced thermogenesis were also unaffected by atropine administration. It is concluded that (1) glucose-stimulated hyperinsulinaemia in human obesity is not dependent on a hyperactivity of the parasympathetic nervous system, which indicates that human obesity is different from most animal models of obesity; (2) glucose-induced thermogenesis is similar in obese and lean subjects when a similar load of glucose is administered; (3) inhibition of the parasympathetic nervous system does not affect the thermic effect of i.v. glucose.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Atropine / pharmacology
  • Blood Glucose / metabolism
  • Body Temperature Regulation / drug effects
  • Body Temperature Regulation / physiology
  • C-Peptide / blood
  • Female
  • Glucose / pharmacology
  • Humans
  • Hyperinsulinism / etiology
  • Insulin / blood
  • Insulin / metabolism*
  • Insulin Resistance
  • Insulin Secretion
  • Male
  • Obesity / complications
  • Obesity / physiopathology*
  • Parasympathetic Nervous System / drug effects
  • Parasympathetic Nervous System / physiology*

Substances

  • Blood Glucose
  • C-Peptide
  • Insulin
  • Atropine
  • Glucose