Differences in adrenergic recognition by pancreatic A and B cells

Science. 1986 May 16;232(4752):875-7. doi: 10.1126/science.2871625.

Abstract

The adrenergic control of glucose homeostasis is mediated in part through variations in the release of pancreatic hormones. In this study, purified pancreatic A and B cells were used to identify the recognition and messenger units involved in the adrenergic regulation of glucagon and insulin release. Catecholamines induced beta-adrenergic receptor activity in A cells and alpha 2-adrenergic receptor activity in B cells. The two recognition units provoked opposite variations in the production of cellular cyclic adenosine monophosphate, the beta-adrenergic unit enhancing the nucleotide's permissive effect on amino acid-induced glucagon release and the alpha 2-adrenergic unit inhibiting that upon glucose-induced insulin release. In both cell types, catecholamines interact powerfully with the synergistic control of hormone release by nutrient- and (neuro)hormone-driven messenger systems.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic beta-Agonists / pharmacology
  • Adrenergic beta-Antagonists / pharmacology
  • Animals
  • Cyclic AMP / analysis
  • Epinephrine / pharmacology
  • Glucagon / metabolism
  • Insulin / metabolism
  • Insulin Secretion
  • Islets of Langerhans / analysis
  • Islets of Langerhans / drug effects
  • Islets of Langerhans / physiology*
  • Male
  • Rats
  • Rats, Inbred Strains
  • Receptors, Adrenergic, beta / drug effects
  • Receptors, Adrenergic, beta / physiology*

Substances

  • Adrenergic beta-Agonists
  • Adrenergic beta-Antagonists
  • Insulin
  • Receptors, Adrenergic, beta
  • Glucagon
  • Cyclic AMP
  • Epinephrine