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Regulation of muscarinic agonist binding by cations and guanine nucleotides
Ist Teil von
European journal of pharmacology, 1983-10, Vol.94 (1), p.59-72
Ort / Verlag
Amsterdam: Elsevier B.V
Erscheinungsjahr
1983
Quelle
Elsevier Journal Backfiles on ScienceDirect (DFG Nationallizenzen)
Beschreibungen/Notizen
EDTA treatment of membrane preparations from rat brain and myocardium reduced the relative proportion of superhigh and high affinity binding sites for muscarinic agonists by up to 60%. This effect was partially or completely reversed by millimolar concentrations of Mg
2+ or Mn
2+. A number of multivalent metal cations gave qualitatively similar effects, yielding stimulation of agonist binding at low concentrations but inhibition at higher concentrations. The divalent cation-linked subpopulation of muscarinic agonist binding sites identified in this study appears to be the primary target for guanine nucleotide inhibition.