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Research ArticleArticle

Pharmacological Analysis of the Novel Mode of Interaction between Xanomeline and the M1 Muscarinic Acetylcholine Receptor

Arthur Christopoulos, Ann M. Parsons and Esam E. El-Fakahany
Journal of Pharmacology and Experimental Therapeutics June 1999, 289 (3) 1220-1228;
Arthur Christopoulos
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Ann M. Parsons
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Esam E. El-Fakahany
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Abstract

Previous findings in our laboratory suggested that the M1muscarinic acetylcholine receptor (mAChR) agonist xanomeline exhibits a novel mode of interaction that involves persistent binding to and activation of the M1 mAChR, subsequent to extensive washout, as well as a possible insurmountable element. In the present study, we examined this interaction in greater detail, using Chinese hamster ovary cells transfected with the genes for the M1mAChR and neuronal nitric oxide synthase. Pretreatment of cells with xanomeline, followed by extensive washout, resulted in elevated basal levels of neuronal nitric oxide synthase activity that were suppressed by the antagonists atropine or pirenzepine in a concentration-dependent manner. Analysis of the data yielded estimates of Schild slope factors and pKB values for the antagonists that were consistent with a model of simple competition between these latter agents and the persistently bound form of xanomeline. The ability of the antagonists to produce parallel dextral shifts of the concentration-response curves to carbachol and xanomeline was also investigated. The interaction between xanomeline and pirenzepine appeared to be insurmountable, but this may have been due to an equilibrium artifact. In contrast, the interaction between xanomeline and atropine conformed to a model of competition, indicating that the mode of interaction of free xanomeline at the M1 mAChR is pharmacologically identical with that of the persistently bound form. Radioligand binding studies also showed that the presence of various concentrations of xanomeline had no significant effect on the calculated affinity of atropine or pirenzepine in inhibiting the binding of [3H]N-methylscopolamine. Overall, these findings suggest that the persistent attachment of xanomeline to the M1 mAChR does not prevent this agonist from interacting with the classic binding site in a competitive fashion.

Footnotes

  • Send reprint requests to: Prof. Esam E. El-Fakahany, Departments of Psychiatry, Neuroscience and Pharmacology, Box 392 Mayo Memorial, University of Minnesota Medical School, Minneapolis, MN 55455. E-mail:elfak001{at}maroon.tc.umn.edu

  • ↵1 This work was supported by National Institutes of Health Grant NS25743.

  • ↵2 Present address: University of Wisconsin-Stout, Biology Department, Menomonie, WI 54751.

  • Abbreviations:
    mAChR
    muscarinic acetylcholine receptor
    CHO
    Chinese hamster ovary
    CCh
    carbachol
    NMS
    N-methylscopolamine
    nNOS
    neuronal nitric oxide synthase
    dpm
    disintegrations per minute
    • Received October 29, 1998.
    • Accepted January 27, 1999.
  • The American Society for Pharmacology and Experimental Therapeutics
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Journal of Pharmacology and Experimental Therapeutics: 289 (3)
Journal of Pharmacology and Experimental Therapeutics
Vol. 289, Issue 3
1 Jun 1999
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Research ArticleArticle

Pharmacological Analysis of the Novel Mode of Interaction between Xanomeline and the M1 Muscarinic Acetylcholine Receptor

Arthur Christopoulos, Ann M. Parsons and Esam E. El-Fakahany
Journal of Pharmacology and Experimental Therapeutics June 1, 1999, 289 (3) 1220-1228;

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Research ArticleArticle

Pharmacological Analysis of the Novel Mode of Interaction between Xanomeline and the M1 Muscarinic Acetylcholine Receptor

Arthur Christopoulos, Ann M. Parsons and Esam E. El-Fakahany
Journal of Pharmacology and Experimental Therapeutics June 1, 1999, 289 (3) 1220-1228;
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