In vivo modulation of the number of muscarinic receptors in rat brain by cholinergic ligands

Eur J Pharmacol. 1981 Aug 27;74(1):73-81. doi: 10.1016/0014-2999(81)90325-3.

Abstract

Administration of the muscarinic agonist oxotremorine led to a decrease in the number of muscarinic receptors, as determined by specific binding of [3H]quinuclidinyl benzilate ([3H]QNB), in several rat brain regions both during development and at maturity. In contrast, administration of the muscarinic antagonist scopolamine led to an increase in the number of [3H]QNB-binding sites in various brain regions. Scopolamine also prevented the decrease in the number of [3H]QNB-binding sites induced by administration of an organophosphorus drug. The results are compatible with the hypothesis that the number of brain muscarinic receptors, or at least of a sub-class of them, is regulated by their transmitter.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholinesterase / analysis
  • Animals
  • Binding Sites
  • Brain / metabolism
  • Ligands
  • Male
  • Organothiophosphorus Compounds / pharmacology
  • Oxotremorine / pharmacology*
  • Quinuclidinyl Benzilate / metabolism
  • Radioligand Assay
  • Rats
  • Rats, Inbred Strains
  • Receptors, Cholinergic / drug effects*
  • Receptors, Muscarinic / analysis
  • Receptors, Muscarinic / drug effects*
  • Scopolamine / pharmacology*

Substances

  • Ligands
  • Organothiophosphorus Compounds
  • Receptors, Cholinergic
  • Receptors, Muscarinic
  • Oxotremorine
  • Quinuclidinyl Benzilate
  • amiton
  • Scopolamine
  • Acetylcholinesterase