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

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.