Muscarinic cholinergic binding in rat brain

Proc Natl Acad Sci U S A. 1974 May;71(5):1725-9. doi: 10.1073/pnas.71.5.1725.

Abstract

Binding sites with high affinity and specificity for [(3)H]quinuclidinyl benzilate (QNB) are present in homogenates of rat brain. The characteristics of the binding sites resemble those of muscarinic cholinergic receptors. Specific binding is saturable with respect to [(3)H]QNB and tissue concentration and is time-, temperature-, and pH-dependent. The bimolecular rate of association (2.0 x 10(8) M(-1) min(-1)) and dissociation (1.2 x 10(-2) min(-1)) at 35 degrees indicate a dissociation constant of 60 pM and a density of 65 pmol/g of brain. Muscarinic antagonists and agonists displace specific [(3)H]QNB binding, while nicotinic and non-cholinergic drugs possess little affinity for [(3)H]QNB-binding sites.

Publication types

  • Comparative Study

MeSH terms

  • Acetylcholine / pharmacology
  • Animals
  • Arecoline / pharmacology
  • Atropine / pharmacology
  • Benzilates / metabolism*
  • Binding Sites
  • Binding, Competitive
  • Brain / metabolism*
  • Brompheniramine / pharmacology
  • Carbachol / pharmacology
  • Chlorpheniramine / pharmacology
  • Hydrogen-Ion Concentration
  • In Vitro Techniques
  • Kinetics
  • Male
  • Methacholine Compounds / pharmacology
  • Microsomes / metabolism
  • Mitochondria / metabolism
  • Oxotremorine / metabolism*
  • Pilocarpine / pharmacology
  • Quaternary Ammonium Compounds / pharmacology
  • Quinuclidines / metabolism*
  • Rats
  • Receptors, Cholinergic*
  • Scopolamine / pharmacology
  • Temperature
  • Time Factors
  • Tritium

Substances

  • Benzilates
  • Methacholine Compounds
  • Quaternary Ammonium Compounds
  • Quinuclidines
  • Receptors, Cholinergic
  • Pilocarpine
  • Tritium
  • Chlorpheniramine
  • Arecoline
  • Oxotremorine
  • Atropine
  • Carbachol
  • Scopolamine
  • Brompheniramine
  • Acetylcholine